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Identify a group of Articles of Diseases

Learn about bone and joint diseases, cancerous tumors, and gynecological diseases, their types, and an article about each of them.

Articles of Diseases : Gynecological diseases

Articles of Diseases

 

New mothers commonly feel a little sad, anxious or tired.as studies show that up to 80 percent of mothers .have these feelings and they last for a week or two after giving birth. which is completely normal and usually disappears within a few weeks. But postpartum depression is another matter entirely. Although some symptoms appear similar. postpartum depression is much stronger and lasts for a longer period. The severity of these feelings. on the mother and make self-care or taking care of the child difficult and difficult.
Postpartum depression should not be taken lightly. It is a serious disorder that may lead a mother to harm her baby or commit suicide.but at the same time it can be overcome with appropriate treatment.
What are the symptoms of postpartum depression?
Most of the symptoms of postpartum .depression are similar to those of normal depression.and knowing the main symptoms .of postpartum depression may help you to recognize the illness early and seek medical help,.which may spare the mother and family long suffering. Symptoms of postpartum depression vary from woman to woman and even from day to day. and the following are the most important and common symptoms:
• Feeling sad or crying, for no apparent reason.
• Exhaustion, inability to sleep.
• Oversleeping.
• Inability to stop eating, or lack of interest in food at all.
• The presence of many aches or pains or unexplained symptoms.
• Irritability, anxiety or anger, without knowing the reason for that.
• Mood swings suddenly and without warning.
• Feeling of losing control.
• Difficulty remembering things.
• Inability to focus or make simple decisions.
• Lack of interest in things the mother would normally enjoy.
• Feeling that there is no real bond with the child.
• Despair and extreme frustration.
• Feelings of extreme guilt.
• The desire to escape from everyone and everything.
• Having urgent thoughts about harming oneself or the newborn.
• Withdrawal from social activities and lack of desire to mix with others.
Symptoms are likely to start within a few weeks of giving birth. Sometimes, postpartum depression doesn’t appear until months later. Symptoms may stop for a day or two and then return. If left untreated, symptoms may continue to worsen.
What causes postpartum depression?
The exact cause of depression is still not completely clear. but it is certain that there are some factors that contribute to the occurrence of postpartum depression. Postpartum depression may be caused by a combination of physical changes and emotional stress.
• Hormonal factors: One of the biggest physical changes a woman faces after giving birth is the change in hormone levels. During pregnancy, estrogen and progesterone levels are higher than normal, and within hours of birth, these hormones drop very quickly, returning to their pre-pregnancy levels. This sudden change sometimes leads to symptoms of postpartum depression. These hormones play a similar role in causing PMS that many women experience, but the changes that occur after childbirth are much stronger.
Other hormones may play a role in depression, especially low levels of thyroid hormone, or what is known as thyroid laziness.
• Lack of sleep.
• Substance misuse and excessive drinking of alcohol.
• The presence of a previous psychological problem increases the possibility of postpartum depression, as women with a previous mood disorder such as depression or bipolar disorder are more likely to occur than others.
• Emotional stressors such as the recent separation from the husband or his death, or family problems. or financial pressures. The lack of support provided by family and close people also plays a role in the occurrence of depression.

What are the ways to treat postpartum depression?
Recognizing the symptoms of postpartum .depression and seeking early medical help is the cornerstone of successful treatment. Treatment depends on two main lines: medication and psychotherapy. A doctor can use either one alone. but treatment may be more effective when used together.and it’s also important to include some healthy choices in your daily routine.
• Medications: Antidepressants have a direct effect on the brain. as they lead to chemical changes in the brain that regulate mood. But the negative point here is that these drugs are generally slow to act. as it takes several weeks from the start of taking the drug until signs of improvement appear. These medications sometimes have side effects including fatigue, decreased libido. dizziness, headache, weight gain, and diarrhea or constipation.
Drug treatment requires cooperation between the doctor, the patient and her family. When the side effects are severe or make the condition worse.the doctor should be informed to adjust the dose, or replace the treatment.
Most antidepressants are safe while you’re breastfeeding. but if you’re breastfeeding, be sure to tell your doctor so he can choose the most appropriate medication. The doctor should also be informed of any existing medical problems such as heart problems or epileptic seizures.
• Psychotherapy: A doctor or psychotherapist .can provide advice on psychotherapy that may help you understand your problem and. provide appropriate strategies for working through it.
• Ensuring a healthy lifestyle: by sticking to a balanced diet and doing some exercise on a daily basis. even if it’s just a walk in the neighborhood. On the other hand, it is important for the mother to get enough rest, although this may be difficult with a newborn baby who needs a lot of care.
Support from family and friends is more important than ever. It is essential that the mother communicates with the people she loves and trusts. understands the nature of her problem and mood swings, and listens to what she is experiencing and feeling.
Treatment helps most women feel better within six months.although it can take longer.

the reviewer:

Twins spread around the world, and although a twin pregnancy is a source of joy and joy for parents, it is considered a worrying factor for doctors, as early birth is a common thing that exposes newborns to many complications, the most important of which are respiratory, digestive and nervous problems, and the mother is also exposed to the risk of gestational diabetes and high blood pressure. blood during pregnancy and others.
Most expectant mothers can reach the end of pregnancy safely, and often complications are simple and treatable if diagnosed early, as newborn jaundice and anemia can be easily treated in most cases, and monitoring and control of sugar and blood pressure numbers in the mother helps to avoid many dangerous complications .
True (identical) twins make up a small percentage of twins, and these twins result from the splitting of a cell mass into two groups, each of which forms an embryo. In some cases, this division fails completely, so the two fetuses remain conjoined and this is known as conjoined twins. What is it and why does it occur?
What are Siamese twins?
Siamese twins or conjoined twins are a rare type of twin in which part of the twins’ bodies are fused together. When this happens, the fusion usually occurs between the same parts of the body, for example between a head and a head or between a chest and a chest. The location and extent of the conjoining varies according to the type of case.
In most cases, there are severe congenital malformations, but advances in medicine and surgery have improved survival rates, and helped surgeons to surgically separate some conjoined twins.
What are the causes of conjoined twins?
This condition occurs in true twins, that is, those that arise from the same egg as a result of the lack of complete separation during the period of fetal life inside the womb. Although the reason is not completely specific, studies accuse the taking of some medications such as clomiphene, which is used to induce ovulation in women in the context of infertility treatment, or in some rare cases after mothers were exposed to valproic acid (sodium valproate), which is used in the treatment of epilepsy, and thistle has also been associated with Clefts in some cases of Siamese twins as well.
One of the misconceptions is that Siamese twins are caused by a genetic condition, as doctors were unable to detect any genes that could be responsible for this condition, and therefore there is no risk of recurrence of the condition in the same family.
What are the symptoms of Siamese twins?
There are no specific signs or symptoms that indicate a conjoined twin pregnancy. As with other twin pregnancies, the uterus is growing faster than a single pregnancy, and there may be more tiredness, nausea, and vomiting early in the pregnancy.
Siamese twins are usually classified according to the place where they are joined, and sometimes they are joined in more than one place. Twins may share one or more parts of the body. Conjoining in Siamese twins occurs in any of the following locations:
• Chest where they may have a common heart and may also share one liver and this is one of the most common locations for Siamese twins.
• The abdomen, where the adhesion occurs near the belly button, and here the twins do not share the same heart, but the liver is common, and they may share a part of the lower intestine.
• The head is in the back, front or side of it, but not the face. Here the twins share part of the skull bone and may share some brain tissue.
• In rare cases, Siamese twins may be conjoined to one twin that is smaller and less formed than the other (non-conjoined twins).
As with twins, conjoined babies are more likely to be born prematurely, and may be stillborn or die soon after birth. Severe health problems for twins such as difficulty breathing, cerebral palsy or heart problems may occur. In the long term, children also suffer from spinal problems such as scoliosis, learning and integration difficulties, and psychological problems.
How are conjoined twins diagnosed?
Siamese twins can be diagnosed using ultrasound as early as the end of the first trimester, and more detailed ultrasound and echocardiography can be used around the middle of pregnancy to determine the connection and functioning of the twins.
If conjoined twins are discovered by ultrasound, magnetic resonance imaging (MRI) may be performed, which may provide more details about where the twins are joined and what organs they share. For the best possible treatment opportunities for children.
How are conjoined twins treated?
Dealing with conjoined twins is difficult and requires a highly experienced medical team to assess the severity of the condition and perform surgery if possible. This team includes obstetricians, pediatricians, neonatal intensive care specialists, cardiologists, thoracic and neurologists, and needs advice from radiologists, nutritionists and psychiatrists.
After the birth of conjoined twins, a full evaluation is made and decisions are made about their care and whether or not separating surgery is appropriate. This surgery may vary depending on exactly how the twins are conjoined, the age of the twins and the maturity of their organs.
In some complex cases, separation is not an option. The more complex the affected device, the more difficult the surgery. The twins may be conjoined at the top of their bodies and share a heart, making it nearly impossible to perform successful surgery, but with the advancement of medicine, more conjoined twins will be Able to benefit from successful separation surgery without any major complications.
the reviewer:

 

The birth of twins is considered a happy event. Having a twin in the house means more joy and joy, and more loving chaos for the parents, especially if the twins are identical so that it is difficult to distinguish between one and the other. Twins share the womb and share food, and later share childhood memories and distinct relationships develop between them, as parents notice a special communication between the twins, and studies indicate the presence of deliberate movements between the twins since the 14th week of pregnancy.
A twin pregnancy is the presence of more than one fetus in the mother’s womb, and these fetuses may be identical or not identical, and in both cases pregnancy is associated with higher rates of complications and complications during pregnancy and childbirth. Why does twin pregnancy occur, and what are its problems?
What is a twin pregnancy?
If two or more babies develop in a woman’s womb at the same time, this is known as a multiple pregnancy. Twins may be twins or triplets, and in rare cases, pregnancy occurs with four or more twins. There are two main forms of twin pregnancy, identical (true) and non-identical twins, and there are some other forms, but they are rare.
• In the case of identical twins, the sperm meets the egg and fertilization takes place to form the first cells that will develop into an embryo. After that, this block of cells divides into two masses forming identical twins, and if one of the two parts of this egg separates again, we have three identical twins and so on. These twins share the same genes, so they have identical morphological features, and it is impossible to differentiate between them in many cases, and identical twins are always of the same sex. Identical twins also share common diseases. If one of the twins shows signs of a genetic disease, the other twin carries a high risk of developing the same disease.
In some cases, the division of the cell mass into two masses is delayed, so the two fetuses share one placenta, and they may be present in one sac sometimes. When the division is delayed more, the twins are born conjoined and this is called Siamese twins, which is a very rare but dangerous condition, as surgeons are unable to separate the two children from each other in many cases.
• As for non-identical twins, they arise from two separate eggs. Where two eggs are released from the ovary, and they are fertilized with two sperms. Therefore, identical twins do not share the same genes, and each of them has its own placenta to be nourished inside the womb in most cases, and the children may be of the same sex or of different sexes.
What are the causes of a twin pregnancy (Multiple Pregnancy)?
Pregnancy with identical twins (true twins) is rare, with an estimated incidence of 1 per thousand births, and the factors that lead to its occurrence are unknown.
While pregnancy with non-identical twins most commonly occurs, it is mainly related to genetics, as it usually occurs in women who have a family history of twins on the mother’s side. The chance of it occurring increases with age, because the ovary releases more than one egg at the same time in older women, and the rate of its occurrence increases in women who received treatment to induce ovulation, especially when resorting to assisted fertilization techniques (IVF) to treat infertility. Food type may play a role in the occurrence of a twin pregnancy, as milk and dairy products may stimulate the ovaries to produce more eggs in one menstrual cycle.
How is a twin pregnancy diagnosed?
The presence of a twin pregnancy is suspected based on several factors such as the presence of twins in the family, or the large size of the uterus relative to the expected gestational age, which may indicate the presence of conditions that lead to excessive enlargement of the uterus, such as a twin pregnancy, ascites, or hydatid molars, or if the woman received A fertility treatment that increases ovarian activity.
But usually the presence of a twin pregnancy can be confirmed through an ultrasound scan, where the doctor can accurately determine the presence of two or more fetuses, and upon examination, it must be determined whether the children share the same placenta or if they have separate placentas.How are twins born?
Although natural childbirth is possible in some cases of twin pregnancies, the rate of resorting to caesarean section may be high, especially in triple pregnancies, in order to avoid serious complications and ensure the safety of the mother and fetuses. Of course, this surgery is done under general or regional anesthesia and in the operating room, in the presence of a specialized and experienced obstetrician.
What are the risks of a twin pregnancy?
Premature birth is one of the most common risks for a twin pregnancy, as the baby is usually born at the completion of (39-40) weeks of gestation, but most twins are born prematurely, that is, approximately before the 37th week of pregnancy. Babies suffer from many problems related to premature birth such as feeding difficulties, insufficient breast milk, newborn jaundice, iron deficiency anemia, and they also have digestive and respiratory problems due to the insufficient maturity of the body’s organs.
Babies born prematurely need to be admitted to the incubators and prematurity department to receive medical care, and some of them may need extreme care and respiratory support, and they are more likely to have long-term problems such as hearing or vision problems or cerebral palsy, and they also suffer from respiratory diseases, the most important of which is asthma in common. Many of these children have developmental problems, learning difficulties, and intellectual disabilities.
Mothers have symptoms of early pregnancy such as nausea, vomiting and extreme tiredness, and may become increasingly constipated. The risk of gestational diabetes, high blood pressure during pregnancy, and gestational toxicity increases, and they are exposed to problems related to the placenta such as placenta previa or premature placental abruption, which causes bleeding in the last months of pregnancy and threatens the life of the mother and fetus. Postpartum depression occurs most commonly.
A twin pregnancy is a difficult pregnancy, and there are many problems and complications that affect the mother and fetuses, so the pregnant mother with twins must be closely monitored, which requires more visits than usual to the obstetrician and gynecologist to follow up the pregnancy, monitor the mother’s condition, and early intervention when necessary.the reviewer:

 

Birth Control is the use of different devices, medications, tools, practices, or surgeries to prevent pregnancy, and it enables people to choose the timing that suits their circumstances to have children. A range of devices and treatments are available for both men and women that can help prevent pregnancy.
No method of contraception is 100% guaranteed, and the quality of each method often depends on adherence and caution when using it. Contraceptive pills, for example, are more than 99% effective if used correctly, but this depends on the woman’s memory and her commitment to taking the medication daily and at a fixed time.
In general, the contraceptive method is divided into traditional practices, barrier devices, medications, and surgical methods. What are each method?
What are the natural means of contraception?
Conventional contraceptive methods do not involve any type of device or medication and include two main methods:
Abstaining: This means avoiding any sexual intercourse at times when a woman’s fertility is high.
• Withdrawal: Also known as intercourse, it means a man pulls his penis out of the vagina so that ejaculation occurs outside the vagina. In theory, this prevents sperm from entering the vagina, but in reality the effectiveness of this method does not exceed 80% only.
What devices can be used?
The barrier devices prevent sperm from reaching the egg. It can be combined with a spermicide, a substance that chemically kills sperm, in order to improve its effectiveness. The most important devices:
• The condom: It forms a barrier and prevents pregnancy by stopping sperm from entering the vagina. It is placed around the penis before sexual intercourse. It is made of polyurethane or latex. Condoms can also help prevent the spread of sexually transmitted infections, and are more than 80% effective in preventing pregnancy. Condoms are widely available in drugstores and stores.
• The female condom: It is made of polyurethane, and has two flexible rings at their ends. One is placed behind the pubic bone to hold the condom in place, while the other is kept outside the vagina. Spermicide can be placed in the vagina before intercourse. The female condom is 79% effective, less available than male condoms and more difficult to use.
• Sponge: It is placed inside the vagina, and it has a depression to be held in place through the cervix. Spermicide foam is put into the vagina using a thin medical device. The sponge acts as a barrier to stop sperm from reaching the egg.
• The veil: It is a rubbery, tip-like device that is placed inside the vagina and fixed through the cervix.
• Intrauterine device (IUD): It is a small, flexible, T-shaped device that is placed in the uterus by the doctor. It has two types:
• A copper coil that releases copper and acts as a spermicide.
• A hormonal IUD contains progesterone. It prevents sperm from reaching and fertilizing an egg by thickening the cervical mucus and making the uterine wall thin.
The IUD stays in place for several years as long as there is no desire to become pregnant, and is 99% effective.
The IUD is generally considered safe, but it may cause heavy menstruation in some women, increase the incidence of ectopic pregnancy, and, in rare cases, lead to infection causing PID.
What drugs and hormones are used to prevent pregnancy?
• Injections: a contraceptive drug that contains progesterone only. The injection is given every 3 months in a doctor’s office. It prevents pregnancy by preventing a woman’s ovaries from releasing eggs. The injections are 94% effective, and the chance of pregnancy increases as the effect of the injection wears off. It is important to remember to schedule your next injection after 3 months to ensure its effectiveness.
• Contraceptive pills: The combined oral contraceptive pill is taken daily, and contains the hormones estrogen and progesterone. The hormones stop ovulation and make the lining of the uterus thin. Its effectiveness ranges between 91-95%.
The contraceptive pill is a popular method and is widely used by women, so its unwanted side effects should be taken into account such as weight gain, high blood pressure, headache and mood disturbance, and may sometimes be associated with more serious problems such as cardiovascular diseases, ischemic heart attacks, and others.
• The contraceptive patch: It is a patch placed on the skin, and it releases the synthetic hormones estrogen and progesterone. A patch is applied every week for three weeks in a row, usually on the lower abdomen or buttocks, and not in the fourth week to allow menstruation to occur. Its effectiveness is estimated at 91%.
• The vaginal ring that contains hormones: It is a flexible plastic ring that releases a low dose of progesterone and estrogen for 3 weeks, preventing ovulation and thickening the cervical mucus, so that sperm cannot move easily. A woman inserts the ring into her vagina for 3 weeks and then removes it for a week. During this week, menstruation occurs.
• The implant: It is a small tube containing progesterone inside the skin of the woman’s upper arm, and its effectiveness lasts up to 4 years, but it can be removed at any time and pregnancy becomes possible. It is 99% effective in preventing pregnancy.
• Emergency contraceptive pill: It can prevent pregnancy after intercourse. It prevents ovulation, insemination, or implantation of the fetus. It can be used within 72 hours of unprotected intercourse, and its effectiveness is 95% during the first 24 hours, and decreases to 60% after that.

Bleeding in the last months of pregnancy is a common occurrence, as one out of every ten women has a vaginal bleeding in the last trimester of pregnancy, and although most of these cases are minor, some of them may be an indication of a serious problem that threatens the safety of The mother and the fetus, so this problem must always be dealt with cautiously and consult a doctor quickly.

What are the causes of bleeding in the last months of pregnancy?

When labor begins, the cervix begins to open or dilate, causing a small amount of blood mixed with normal vaginal secretions or mucus to come out, which is normal. Bleeding in the last months of pregnancy can also be caused by:

Having sex and causing a slight bleeding of several points of blood.
Internal examination by a doctor.
Diseases or infections affecting the vagina or cervix.
Uterine fibroids.
Having a problem in the cervix, such as cervical cancer.
More serious causes of bleeding in the last months of pregnancy may include:

Placental abruption: It is the most common cause of life-threatening bleeding in the last months of pregnancy, and it accounts for about 30% of cases, and it can happen at any time, but it is more common in the last trimester of pregnancy. It occurs when the placenta separates from the inner wall of the uterus before the baby is born, and this separation causes vaginal bleeding, abdominal and back pain.
The reason for this separation is not clear, but it may occur because the blood supply to the placenta is insufficient, or the placenta may sometimes separate after an injury such as a car accident. Separation can occur in any woman, but it is more common in some cases, such as:

Chronic high blood pressure.
Gestational hypertension, especially if it is accompanied by complications such as preeclampsia.
Age greater than 35 years.
smoking.
Placental abruption in a previous pregnancy.
The bleeding may be more severe than it appears, because most of the blood may be trapped behind the placenta, and therefore it is not visible and cannot be estimated. On the other hand, the fetus is not able to obtain an adequate amount of blood, which threatens its safety and life.

Placenta previa: It is a pregnancy problem in which the placenta grows in the lower part of the uterus instead of the upper part, when the placenta may partially or completely block the cervix (the lower part of the uterus), which is the passage through which the fetus passes. In many cases, the placenta rests on the lower part of the uterus at the beginning of pregnancy, but it automatically moves upward as the uterus grows and expands.
When labor begins, the cervix dilates, capillaries in placenta previa rupture, and bleeding begins. This bleeding may occur after an internal examination, or for no apparent reason.

In most cases, the lower placenta accreta is known to the mother and the doctor before the bleeding begins, through ultrasound imaging, which is done to routinely monitor pregnancy, so the mother must be careful, monitor the bleeding, and inform the doctor if it occurs.

Placenta previa tends to occur in women older than 35, especially women who smoke. It also occurs when there is a scar on the uterus as a result of a previous cesarean section, or a fibroid removal, or when there is a twin pregnancy.

Vessels advanced on the fetus: a condition in which the blood vessels that deliver blood to the fetus (through the umbilical cord) grow above the cervix, blocking the fetus’s transit route. When labor begins, these vessels may rupture, depriving the fetus of blood. This condition is often associated with placenta previa, a twin pregnancy, or treatment of infertility with in vitro fertilization techniques (IVF).
The fetus depends entirely on the placenta for its nutrition, so the loss of any amount of blood is considered dangerous, even if it is small.

Uterine rupture: Uterine rupture may occur during labor, and it often affects women who have scars on the uterus such as a previous caesarean scar or surgery for any reason, or after severe trauma to the abdomen such as a car accident, and it may occur when labor is violently induced.
How is the diagnosis of bleeding in the last months of pregnancy?

The doctor first asks questions about the bleeding and other symptoms and the medical history, and then performs some tests such as blood tests to assess the degree of anemia, and ultrasound to assess the position and vitality of the fetus and to assess the position of the placenta. A transvaginal ultrasound can provide more accurate information about the cause of the bleeding and the location of the placenta, umbilical cord, and blood vessels.

How is the treatment of bleeding in the last months of pregnancy?

In the event of placenta abruption or placenta previa, it is recommended that you rest in bed in the hospital, where the mother and fetus can be monitored, and treatment given promptly if necessary. The pregnant woman may be discharged home when the situation is stable and the bleeding has stopped in some cases. While doctors prefer to terminate the pregnancy if the fetus is mature enough, or the bleeding is severe, and this is usually done by cesarean section.

Uterine rupture is an emergency situation that threatens the life of the mother and fetus, so a cesarean section must be performed quickly, after which the ruptured uterus can be repaired, and the doctor may have to perform a hysterectomy in some cases.

the reviewer:

High blood pressure during pregnancy is a common disease that affects many pregnant women, and despite the fact that its complications and complications are numerous, good control of high pressure and adherence to the doctor’s instructions and medications avoid complications for the patient.

 

Pre-eclampsia is one of the worst problems that can happen to pregnant women during pregnancy, and it may be the worst of all. Preeclampsia usually occurs in women who suffer from uncontrolled high blood pressure during pregnancy. What is preeclampsia, what are its symptoms, and how can it be prevented?

What is pre-eclampsia?

One of the worst problems of pregnancy, preeclampsia is characterized by gestational hypertension and is associated with signs of damage to other organ systems, including the kidneys, liver, blood and brain.

Pre-eclampsia is called pre-eclampsia, or pre-eclampsia, because untreated cases of it may develop serious – or even fatal – complications for the mother and the baby, including eclampsia. Eclampsia is a state of continuous convulsions in the mother that threatens her life.

Who are the women eligible for the risk of preeclampsia?

Preeclampsia occurs in women who suffer from high blood pressure during pregnancy, especially in those who have been diagnosed with high blood pressure before the 30th week.

Some women face a higher risk of pre-eclampsia, including:

Women who had pre-eclampsia in a previous pregnancy.
Women who suffer from chronic high blood pressure, migraines, diabetes, kidney problems, or lupus.
First pregnancy or pregnancy with twins.
Women who are overweight or obese.
Ladies over 35 years old.
Women who have become pregnant using assisted reproductive technology.
What are the symptoms of pre-eclampsia?

Symptoms of pre-eclampsia or pre-eclampsia include:

Abnormal swelling of the hands and face.
continuous headache.
Seeing points or changes in vision.
Upper abdominal pain.
Nausea or vomiting at the end of pregnancy.
Difficulty breathing due to fluid buildup in the lungs.
Decreased urine output.
What are the complications of preeclampsia?

Preeclampsia causes a number of complications, the most important of which are:

Complications for the fetus: High pressure impedes the delivery of blood in sufficient quantities to the fetus, and the fetus does not grow in a good way, which leads to a decrease in birth weight. On the other hand, doctors are forced to terminate the pregnancy early in many cases, as the child is born incomplete and is exposed to more problems than full-developed children, such as neonatal jaundice, respiratory distress, and others.
Complications that occur to the mother: Preeclampsia causes damage to the body’s organs, especially the heart, kidneys, liver, lungs, and eyes. Stroke can also occur.
Placental abruption is an emergency situation in which the placenta separates from the uterus before delivery, which may cause severe bleeding and threaten the death of the fetus.
Eclampsia, which is continuous and dangerous seizures.
HELLP syndrome, characterized by hemolysis, elevated liver enzymes, and low platelet counts, may develop. HELLP syndrome is very dangerous, and requires urgent and emergency treatment, and the doctor may have to terminate the pregnancy.
How is preeclampsia diagnosed and monitored for its development?

When high blood pressure during pregnancy, the doctor will likely want to do some tests, including:

Urine test for protein.
Blood tests to assess liver and kidney function and platelet count.
Simple chest x-ray to check for pulmonary edema, which is the presence of fluid in the lung.
Monitoring the growth of the fetus and the amount of amniotic fluid by ultrasound, and the doctor may order a Doppler image to assess the passage of blood through the placenta.
In some cases, the doctor resorts to special tests to monitor the heartbeat of the fetus.

How is preeclampsia treated?

Women who are diagnosed with preeclampsia face a difficult task, as the disease usually develops with the progression of pregnancy and the doctor may want to terminate the pregnancy quickly, but the interest of the fetus requires staying in the womb to ensure the adequate maturity of the newborn’s organs, as the birth of a child prematurely carries with it the dangers of prematurity and its many problems. Doctors try to ensure the interest of the fetus, provided that the mother is not harmed, and this is a difficult equation.

In most cases, preeclampsia clears up at or shortly after birth. When deciding on treatment, your doctor will consider several factors, such as the severity of the condition, the number of weeks pregnant, and potential risks to you and your baby:

If you’ve been more than 37 weeks pregnant, the doctor will probably want to deliver the baby, because the fetus is mature enough to survive outside the womb.
If you were less than 37 weeks pregnant, your doctor will monitor you and your baby carefully. This includes blood and urine tests for you. Monitoring your baby often includes an ultrasound of the abdomen and monitoring of the baby’s heart rate and growth.
Your doctor may want to deliver the baby early if the condition is severe.
You may need medications to control your blood pressure, steroid injections to help the fetus’s lungs mature faster, and in some cases, preventative anticonvulsants.

Symptoms usually disappear within 6 weeks of birth. In rare cases, symptoms may not go away or may start late after birth, so the mother should be monitored for several weeks after birth.

Can preeclampsia be prevented?

There are no effective and guaranteed ways to prevent preeclampsia, but in general, doctors advise pregnant women to eat a healthy diet rich in vegetables, fruits and whole grains, and to avoid smoking. Your doctor may prescribe low-dose aspirin, or calcium and vitamin D, to prevent preeclampsia.

In fact, the most important step is to monitor the arterial pressure, adhere to the medications prescribed by the doctor, and get good prenatal care to avoid any complications before they occur.

 

the reviewer:

Hypertension is a health concern for many, as it is one of the most common diseases associated with the occurrence of many diseases and complications. High blood pressure during pregnancy is common, and it can pose a double risk, as it affects the health of the mother and her fetus. This condition is a serious concern for some pregnant women, so it is important to recognize and treat it to avoid its effects.What are the causes of high pressure during pregnancy?

 

The cause of high blood pressure during pregnancy is not entirely known, but it is believed that some factors increase the likelihood of it rising: being overweight or obese, not doing enough physical activity, smoking, drinking alcohol, and having a family history of high blood pressure during pregnancy. Pregnancy, diabetes, kidney disease, or an autoimmune disease. It also increases in women who are carrying twins.

What are the normal blood pressure numbers when pregnant?

In fact, blood pressure tends to drop at the beginning of pregnancy, because pregnancy hormones cause the vessels to relax and dilate, which lowers blood pressure. Low blood pressure may cause a feeling of dizziness, tiredness and cold in pregnant women.

As the pregnancy progresses, the pressure rises slightly, but it decreases again after childbirth to return to its normal values. High pressure during pregnancy is due to several reasons, the most important of which are:

The volume of blood increases, and the volume may increase to 150% of its volume before pregnancy.
The work of the heart increases to be able to meet the needs of the mother and the fetus, and this increase leads to a slight enlargement of the heart muscle, which disappears spontaneously after birth.
The kidneys secrete vasopressin, a hormone that traps water in the body, causing swelling and swelling in the ankles and feet.
What are the types of high pressure during pregnancy?

High blood pressure is generally defined as blood pressure greater than 140/90 mmHg, and high blood pressure during pregnancy is divided into several types:

Chronic high blood pressure: Some women have pre-existing high blood pressure before they became pregnant. This condition can be referred to as chronic high pressure, and it is usually treated with appropriate high pressure medications. High pressure in the first 20 weeks of pregnancy indicates that this rise is chronic and has nothing to do with pregnancy.
Gestational hypertension: Gestational hypertension develops after the 20th week of pregnancy and usually disappears after delivery. Gestational hypertension can cause serious complications, the most important of which is preeclampsia.
Preeclampsia, called pre-eclampsia, is a dangerous condition of high gestational pressure associated with the presence of protein in the urine, and leads to many problems and complications.
How is high blood pressure diagnosed during pregnancy?

Your doctor checks your blood pressure at every visit during pregnancy, and compares the result to your pre-pregnancy pressure. The pressure is considered elevated if it is more than 15 mmHg higher than the pre-pregnancy pressure. In general, the pressure is considered high if it is higher if the blood pressure reading is equal to (130/80) or higher, while it is considered very high if it is higher than (140/90).

If your blood pressure is high, the doctor will want to perform some tests, including blood tests and other laboratory tests to look for excess protein in the urine to check for signs of preeclampsia.

What are the complications of high pressure during pregnancy?

High pressure during pregnancy can cause gestational toxicosis (called pre-eclampsia), in which kidney and liver function is damaged, and it may develop into a worse condition, and lead to convulsions or what is called eclampsia. Gestational eclampsia is a serious and potentially fatal condition for both the mother and the baby.

Therefore, doctors classify the pregnancy with high blood pressure as a high-risk pregnancy, and monitor the development of the condition by repeatedly measuring pressure, monitoring kidney and liver function, and checking for protein in the urine. Doppler ultrasound is also required to measure the quality of blood passing through the placenta.

How is high blood pressure treated during pregnancy?

Some traditional blood pressure medications can cause problems in pregnant women and are not recommended, as they are able to pass through the placenta and reach the fetus, which negatively affects it. High blood pressure during pregnancy is treated with special medications. Methyldopa and labetalol are both safe to use to control blood pressure during pregnancy.

Doctors advise taking other steps to treat preeclampsia, and may prescribe aspirin or calcium with vitamin D to prevent its development.

What are the points to remember?

There are a set of recommendations that can reduce the problems and complications of high pressure during pregnancy, including:

If you suffer from high blood pressure, consult your doctor when planning pregnancy. Your doctor will replace your medications with medications that are safe for the fetus.
Monitor blood pressure at home during pregnancy.
To get accurate readings, make sure to measure the pressure while sitting in a comfortable position, and try to take the measurement at the same time daily and in the same arm, and if you notice a rise in pressure, consult your doctor.

Consult your doctor immediately if you experience a severe headache, blurred vision, or abdominal pain. These symptoms may indicate the presence of preeclampsia.
It is important to get prenatal care, make sure you see your doctor and take your medication regularly.
Avoid gaining weight, and stick to a healthy diet rich in vegetables, fruits and whole grains.
Avoid smoking and alcohol completely during pregnancy.
Breastfeeding is important for the child, and there is nothing to impede breastfeeding in case of high pressure, but it is important to consult a doctor about the medications allowed during the breastfeeding period.
the reviewer:

Congenital anomalies in the Female Reproductive System are developmental disorders that affect a girl’s reproductive organs, and occur during her development inside her mother’s womb. The female reproductive organs include the vagina, ovaries, uterus, and cervix.

 

What are the causes of birth defects in the female reproductive system?

A baby’s genitals begin to form between weeks 4 and 5 of pregnancy and continue until week 20. Development is a complex process and many things can affect this process. The severity of your child’s condition depends on when the disorder occurred. In general, if problems occur early in pregnancy, the effect will be wide-ranging.

The reproductive system develops close to the urinary system, so congenital defects of the urinary system and the spine are common concomitantly.

Problems with the development of a girl’s reproductive organs can result from:

A defective or deficient gene (genetic defect) occurs in several cases, including congenital adrenal hyperplasia.
Use of certain medications during pregnancy.
What are the symptoms of birth defects in the female reproductive system?

Some birth defects of the female reproductive system may be asymptomatic. Some symptoms may appear early or at puberty, while others appear late. They are diagnosed when a woman complains of gynecological problems such as endometriosis, infertility, or repeated miscarriages. Symptoms vary according to the type of deformity present, and may include:

Inability to empty the bladder.
Breasts not growing.
Repeated premature births or miscarriages.
Monthly cramps or pain without menstruation.
Abdominal swelling often caused by blood or mucus that cannot escape.
Pain during intercourse.
infertility;
What are the types of birth defects in the female reproductive system?

Birth defects of the female reproductive system include:

cloacal anomalies: The cloaca is a tube-like structure. In the early stages of embryonic development, the urinary tract, rectum, and vagina empty into this single tube, but later they separate and each has its own opening. If the cloacal continues as the baby grows in the womb, the three openings do not form and separate. For example, a baby girl may be born with a single opening near the rectal area, and urine and stool cannot drain from the body, causing the abdomen to swell. These congenital malformations are rare.
Disorders of the external genitalia (visible): Developmental problems can lead to enlargement of the clitoris or fusion of the labia. Labia prolapse is a condition in which the folds of tissue surrounding the opening of the vagina stick together. Most other birth defects of the female reproductive system are associated with hermaphroditism and ambiguous genitalia.
Non-perforated hymen: The hymen is a thin tissue that partially covers the opening of the vagina, and has one or more openings that allow menstrual blood to pass through. Some females are born without a hymen, and this case is not considered rare, while the membrane is not perforated in others, and then the girl complains after puberty of abdominal pain that recurs monthly without menstruation. In fact, menstruation occurs, but blood collects inside the body because there is no opening to allow it to exit.
Ovarian disorders: A girl may carry an extra ovary, extra tissue attached to one of the ovaries, or a structure called the ovarian testis, which contains both male and female tissue.
Uterine and cervical disorders: A baby may be born with an extra uterus and cervix, a semi-formed uterus, or a uterine blockage. Usually, girls born with half a uterus and half a vagina also lack a kidney on the same side of the body. Some girls may have a heart-shaped uterus, or a uterus with a septum in the middle of its cavity called a bicornuate uterus. The two-horned uterus is smaller, so the fetus cannot grow well, so abortion is common, and the fetus may grow for several months, but it is born early.
Vaginal disorders: The baby may be born without a vagina or the vaginal opening is clogged with a layer of cells higher than the site of the hymen. An absent vagina is often the result of Mayer-Rokitansky-Küster-Hauser syndrome. In this syndrome, part or all of the internal reproductive organs (uterus, cervix, and fallopian tubes) are missing in a girl. Other abnormalities include the presence of two vaginas, or a vagina that opens into the urinary tract.
How are birth defects diagnosed in the female reproductive system?

The doctor may notice signs of birth defects right when the baby is born. These signs include:

Genitals It is difficult to determine whether it is male or female (ambiguous genitals).
Labia stuck together or abnormally sized.
The absence of openings in the genital area or the presence of a single rectal opening.
An abnormal vagina.
Bladder outside the body.
Enlargement in the groin or abdomen.

Diagnosing congenital malformations of the female reproductive system requires a wide range of examinations, including:

Laparoscopy.
Chromosome determination, a genetic test.
Hormone levels, especially testosterone and cortisol.
Ultrasound or magnetic resonance imaging (MRI) of the pelvic region.
How are congenital defects in the female reproductive system treated?

Doctors often suggest surgery as a treatment for congenital defects of the female reproductive system. Surgery for some defects can be done while the baby is still a baby, while others can be delayed until the baby is older. Some surgeries can be very complex, and doctors may not be able to do much in complicated cases such as an absence of the uterus.

Early diagnosis is especially important in the case of ambiguous genitalia. The doctor must examine the child carefully before deciding whether it is male or female, this is called gender determination and depends on the results of the clinical examination, chromosomes, hormone tests and X-ray results. Treatment should also include psychological counseling for the parents, and the child should also undergo counseling when she grows up.

the reviewer:

Diagnosing congenital malformations of the female reproductive system requires a wide range of examinations, including:

Laparoscopy.
Chromosome determination, a genetic test.
Hormone levels, especially testosterone and cortisol.
Ultrasound or magnetic resonance imaging (MRI) of the pelvic region.
How are congenital defects in the female reproductive system treated?

Doctors often suggest surgery as a treatment for congenital defects of the female reproductive system. Surgery for some defects can be done while the baby is still a baby, while others can be delayed until the baby is older. Some surgeries can be very complex, and doctors may not be able to do much in complicated cases such as an absence of the uterus.

Early diagnosis is especially important in the case of ambiguous genitalia. The doctor must examine the child carefully before deciding whether it is male or female, this is called gender determination and depends on the results of the clinical examination, chromosomes, hormone tests and X-ray results. Treatment should also include psychological counseling for the parents, and the child should also undergo counseling when she grows up.

the reviewer:

Infertility is one of the most important problems facing people. The instinct of motherhood is an instinctive instinct in women, and the denial of having a child may be one of the most difficult obstacles a woman faces in her life.Infertility is not only a female problem, men can also be sterile. In fact, it is possible for men and women to suffer from infertility equally. About a third of infertility cases are associated with female problems, and another third are related to male problems. The remaining third of cases may be caused by a mixture of male and female infertility, or the cause may not be known. And we will talk here about infertility in women.

 

What is infertility?

Infertility is the inability to conceive after a year of trying without using any form of contraception. Women who become pregnant but do not reach full pregnancy may be diagnosed with infertility as well. A woman who has never been pregnant before is diagnosed with primary infertility, and a woman who has had at least one successful pregnancy will be diagnosed with secondary infertility.

Female infertility can result from a combination of factors that affect or interfere with the following biological processes:

Ovulation, which is the release of a mature egg from the ovary.
Fertilization, which occurs when sperm meets an egg in the fallopian tube after it has traveled through the cervix and uterus.
Implantation, which occurs when a fertilized egg attaches to the uterine lining where it grows into an embryo.
What are the causes of infertility in women?

Infertility is a common condition, as many women face difficulty in getting pregnant, and this percentage increases due to the tendency of women to postpone marriage and pregnancy in their desire to work and build a professional future. Fertility decreases with age, and various factors such as smoking, drinking alcohol, and obesity or excessive thinness.

There are many diseases that lead to a disturbance in the occurrence of pregnancy and that affect the three main steps (ovulation, fertilization, implantation), and the most important of these diseases are:

Hormonal disorders such as polycystic ovary syndrome (PCOS), or prolactinoma (a tumor in the pituitary gland) that leads to high prolactin, hyperthyroidism, or hypothyroidism, and others.
Impairment of ovulation due to premature ovarian insufficiency, which occurs in many cases, including exposure of the pelvis to radiation, which leads to damage to the ovaries.
Uterine abnormalities: In some cases, a healthy uterine fibroid can block the fallopian tubes and prevent fertilization.
Blockage of the fallopian tubes so that the egg is unable to meet the sperm and often occurs after inflammation in them, or adhesions in the pelvis due to endometriosis (which is the presence of the lining of the uterus abscess), or as a result of inflammation in the peritoneum, or after a surgical operation such as an appendectomy or surgery on the Abdomen and pelvis.
Congenital malformations of the female reproductive system.
Some medications can negatively affect fertility, including chemotherapy for tumors, some psychiatric medications, or drug and drug abuse.
How is infertility diagnosed?

The doctor will take your medical history and conduct an examination of the pelvic area to look for any abnormalities. The doctor will also order a set of auxiliary tests, the most important of which are:

Monitoring ovulation Although this is possible using a home device, the most accurate way is to monitor ovulation with ultrasound imaging and laboratory blood tests to assess the status of hormones.
Ultrasound to examine the ovaries and uterus.
Hysterosalpingography, or hysterosalpingogram, is a type of X-ray used to evaluate the fallopian tubes and uterus.
Laparoscopy, which uses a camera to examine internal organs.
Hormonal analyzes and ovarian reserve (AMH) tests. These analyzes are useful in estimating the expected number of years of ovarian activity and determining the possibility of pregnancy in a woman. AMH naturally decreases with age, but when it drops sharply, it indicates that the eggs in the ovaries are almost depleted.
How is infertility treated?

The type of treatment depends on a number of factors, the most important of which are the cause of infertility and the age of both partners. Both partners must take the decision that suits them after knowing the appropriate treatment options.

It is possible to resort to drug treatment, which depends mainly on stimulating or regulating ovulation, while surgery is used in a few cases, such as correcting uterine abnormalities, or opening the blockage in the fallopian tubes.

Science has made great advances in the field of infertility treatment, which has given many hopes. Reproductive assistance includes multiple methods, such as intrauterine sperm injection, where millions of sperm are injected into the uterus near the time of ovulation. In the most difficult cases, doctors resort to the in vitro fertilization technique, or the so-called in vitro fertilization, and this technique depends on taking the mother’s eggs after inducing ovulation for several Days and fertilization with sperm taken from the father in the laboratory, and after vaccination, the fetus is returned to the uterus.

When should a woman seek medical advice?

Doctors prefer to wait for a year after marriage, provided that the couple does not use any method of contraception. But in some cases, the woman should not wait for a year, as it is preferable to visit the doctor before that, and the most important of these cases are:

Six months have passed since marriage for a woman over 35 years old.
Having severely painful or irregular menstrual cycles.
History of a previous cancer.
A history of repeated miscarriages.

the reviewer:

Although the word tumor is associated in the minds of people with a cancerous or serious problem, some tumors are characterized by being healthy, and they may exist in the body for many years without causing any symptoms. One of the most common benign tumors in the body is uterine fibroid.
What are uterine fibroids?
Uterine fibroids are tumors that grow in or on a woman’s uterus. Sometimes these tumors become very large and cause severe abdominal pain and menstrual bleeding, and in other cases they cause no symptoms or signs at all. These tumors are usually benign or noncancerous.
Fibroids are known by many names, including: leiomyomas, uterine myomas, fibroids.
What are the types of uterine fibroids?
The type of fibroid that a woman develops depends on its location in or on the uterus.
• Uterine fibroids within the muscle of the uterus: It is the most common type of fibroids. This type appears inside the muscular wall of the uterus, and the tumor may grow to a large degree, causing an expansion and enlargement in the size of the uterus.
• Subserosal uterine fibroids: Subserosal fibroids form on the outside of the uterus, and the uterus appears asymmetrical if these tumors are large.
• Submucosal fibroids: This type of tumor forms in the middle muscular layer of the uterus, and is the least common type.
What are the causes of uterine fibroids?
It’s not clear what causes uterine fibroids, but several factors influence their formation, including:
• Hormones: The ovaries produce the hormones estrogen and progesterone, which cause the lining of the uterus to regenerate during each menstrual cycle, and may stimulate the growth of fibroids.
• Family history: Fibroids may affect families. If your mother, sister, or grandmother has a history of this condition, it may affect you, too.
• Pregnancy: Pregnancy increases the production of estrogen and progesterone in your body. Tumors can form and grow rapidly during your pregnancy.
• Obesity.
What are the symptoms of uterine fibroids?
Your symptoms will depend on the number of tumors you have, as well as their location and size. For example, submucous fibroids may cause heavy menstrual bleeding and problems getting pregnant. While small tumors do not cause any symptoms. Fibroids may shrink during or after menopause, because women at this stage experience a decrease in the level of estrogen and progesterone, the two hormones that stimulate the growth of fibroids.
Symptoms of uterine fibroids include:
Heavy bleeding between or during menstruation. Heavy bleeding may cause anemia.
• Pain in the pelvis or lower back.
• Increased menstrual pain.
• Pain during intercourse.
• Pressure or fullness in the lower abdomen.
• When the tumor is large, it presses on the bladder, causing an increase in the number of urination times.
• Swollen or enlarged abdomen.
How are uterine fibroids diagnosed?
For a proper diagnosis, you should see a gynecologist for a pelvic examination to determine the condition, size and shape of the uterus. You may also need other tests, including:
• Ultrasound imaging: Ultrasound imaging can be done by placing a probe on the abdomen, or through the vagina. Imaging allows the doctor to see the structure of the uterus, determine the presence of any fibroids, and can determine their number, measure them, and monitor their growth.
• Magnetic resonance imaging of the pelvis (MRI): Magnetic resonance imaging gives clear and accurate images of the uterus, ovaries and other pelvic organs.
Do fibroids cause problems during pregnancy and childbirth?
Fibroids rarely cause infertility, and most women are able to become pregnant and give birth safely.
But large tumors can cause some problems, as they take up a large space in the uterine cavity, which prevents the fetus from taking a position that allows it to give birth naturally, and the rate of caesarean section increases. On the other hand, the supply of the placenta can be affected if it is located directly above the fibroid, so the possibility of early placental abruption, a condition that causes bleeding in the last months of pregnancy, and threatens the safety of the fetus, increases. Therefore, it is important to monitor the size of the fibroid during pregnancy by ultrasound.
How are uterine fibroids treated?
The doctor sets a treatment plan based on your age, the size of your fibroids, and your health condition. Accordingly, the doctor will present a set of options, the most important of which are:
• Monitoring: If you do not have any symptoms, or your symptoms are mild and manageable, the best option may be to wait and watch.
• Medications: Your doctor may prescribe medications to regulate your hormonal levels and thus reduce tumors.
• Surgery: Surgery can be done to remove large or multiple uterine fibroids. This is known as myomectomy. Abdominal myomectomy involves making a large incision in the abdomen to gain access to the uterus and to remove the fibroids. This surgery can also be done through endoscopy, where several small incisions are made and surgical tools and a camera are inserted. The problem of fibroids is that they are reversible, and it is common for them to reappear after they have been removed.
• The doctor may present the option of hysterectomy, especially in severe cases of tumors that cause severe bleeding and anemia. Of course, a hysterectomy will cause permanent infertility, so doctors prefer to perform it after menopause.
Some options can relieve symptoms such as bleeding and pain, but they do not shrink or remove fibroids. These include:
• A hormonal IUD containing progesterone.
• Non-steroidal anti-inflammatory drugs, which are taken without a prescription, such as ibuprofen, but these drugs should be avoided in patients with peptic ulcer and asthma.
• Contraceptive pills.

 

the reviewer:

Abdominal pain is a common symptom, and we all suffer from it from time to time. Abdominal pain may go away spontaneously or by taking simple painkillers, but in some cases it may be an indication of a dangerous condition, including ovarian torsion in women.
What is ovarian torsion?
Ovarian torsion occurs when the ovary wraps around the tissues that support it and provide blood flow to the ovary. This torsion leads to the interruption of blood from the ovary, causing ischemia, and this may lead to tissue necrosis in the ovary and its death, and consequently, the loss of the ovary if it is not treated correctly and in the right time.
In some cases, the ovary twists again in the opposite direction automatically, and the blood supply returns, and the symptoms disappear without any treatment.
You’re more likely to develop ovarian torsion if you have ovarian cysts, which can cause ovarian swelling. You can reduce your risk of ovarian torsion by using birth control pills or other medications to help reduce the size of the cysts.
What are the symptoms of ovarian torsion?
Ovarian torsion causes severe pain in the lower abdomen, which occurs suddenly and without warning, and is accompanied by nausea and vomiting.
This condition is never without pain. If you have nausea and vomiting without pain, you probably have a different condition. In either case, you should see a doctor.
What are the causes of ovarian torsion and risk factors?
Ovarian torsion can occur if the ovaries are not stable. An enlarged ovary can tilt slightly and is at risk of torsion. This occurs in the following cases:
• The presence of a cyst in the ovary.
• Polycystic ovary syndrome (PCOS).
• The presence of a long ovarian ligament, which is the fibrous stalk that connects the ovary to the uterus.
• Pregnancy, as pregnancy hormones may cause some swelling in the ovaries.
• Hormonal treatment for infertility, which may stimulate the ovaries.
Although this condition can occur in women and girls of any age, it is more likely to occur during the childbearing years.
How is ovarian torsion diagnosed?
If you have severe abdominal pain, seek immediate medical attention. The longer it takes before the condition is treated, the more complications you will experience. After evaluating your symptoms and reviewing your medical history, your doctor will perform a pelvic exam to pinpoint the locations of your pain.
In fact, diagnosing ovarian torsion is difficult in many cases, as the symptoms are very similar to a number of diseases that lead to acute abdominal pain, including:
• Urinary infections such as pyelonephritis.
• Ovarian abscess.
• Ectopic pregnancy.
• Appendicitis.
• Kidney stones.
Doctors usually use a number of auxiliary tests, such as blood and urine analysis to rule out urinary infections, and ultrasound or magnetic resonance imaging (MRI) to assess the condition of tissues inside the abdomen and pelvis. But despite all that, the only way to confirm the diagnosis is to perform surgery when a warp is suspected and corrected.
How is ovarian torsion treated?
Surgery is the only solution to ovarian torsion. The surgeon removes the torsion by laparoscopic or conventional surgery.
• Endoscopy: The doctor inserts a thin, lighted instrument into a small incision in your lower abdomen, allowing the doctor to see your internal organs. Another cut will be made to allow it to reach the ovary, then a blunt probe or other instrument will be used to loosen the warp. This laparoscopic surgery is usually done under general anaesthesia.
• Conventional surgery: With this operation, the doctor will make a larger incision in the lower abdomen to allow him to access the ovary and manually untie the warp.
If it has been a long time since the torsion, and the prolonged interruption of blood supply causes death of the ovarian tissue, the doctor may need to remove the ovary.
It is usual to prescribe analgesic medications to relieve pain such as non-steroidal anti-inflammatory drugs such as ibuprofen, and the doctor may need to administer more powerful drugs such as opioids.
It’s common for a doctor to prescribe medications to reduce the risk of recurrence, such as high doses of contraceptives or other forms of hormonal birth control.
What are the complications of ovarian torsion?
The longer it takes before diagnosis and treatment, the more ovarian tissue is at risk. When torsion occurs, the ovarian blood supply is reduced, and ischemia can also affect the fallopian tube. Prolonged ischemia may lead to necrosis (tissue necrosis). If this happens, oophorectomy is necessary.
The only way to avoid these complications is to seek immediate medical help if symptoms appear.
Ovarian torsion does not cause infertility, and does not affect fertility in any way. Even if the ovary is lost, the second ovary remains functional.

 

the reviewer:

A woman’s body, especially during the childbearing years, is subject to a delicate hormonal balance, and any imbalance in this balance will lead to an imbalance in the body and its vital functions, including childbearing.
Polycystic ovary syndrome is one of the common hormonal disorders, which leads to the emergence of masculine characteristics, and may cause infertility in some cases. What is it, what are its symptoms and ways to treat it?
What is polycystic ovary syndrome?
Polycystic Ovary Syndrome, also referred to as PCOS, is a condition that affects a woman’s hormone levels during the reproductive years, as a woman’s production of male hormones increases. A hormonal imbalance causes irregular periods and makes it difficult to get pregnant.
Polycystic ovary syndrome also causes facial and body hair growth and baldness, and contributes to long-term health problems such as diabetes and heart disease. Birth control pills and diabetes medications can help repair a hormonal imbalance and relieve symptoms.
What are the causes of polycystic ovary syndrome?
The cause of Polycystic Ovary Syndrome is not known precisely, but genes have been accused of contributing to its occurrence. There is a disturbance in two main hormones in this syndrome, which are:
• High levels of male hormones prevent the ovaries from producing hormones and making eggs normally.
• About 70% of women with this syndrome have insulin resistance, which means that their cells do not use insulin properly.
When cells don’t use insulin properly, the body’s need for insulin increases, causing the pancreas to produce more insulin to compensate. Increased insulin stimulates the ovaries to produce more male hormones.
What are the symptoms of polycystic ovary syndrome?
It is possible for the patient to notice the symptoms when the menstruation occurs for the first time, but some patients do not know of their infection until after they gain weight or face difficulties in getting pregnant.
Common symptoms of polycystic ovary syndrome include:
• The high male hormone causes the emergence of masculine characteristics such as hair growth on the face and body, including the back, abdomen, and chest, and the sudden appearance of acne on the face, chest and upper back, and baldness.
• Menstrual cycle disorder: Ovulation does not occur normally as a result of the existing hormonal disturbance, so it is common for menstrual cycles to be spaced and irregular. Some women with this syndrome have fewer than 8 menstrual cycles per year.
On the other hand, the uterine lining grows longer than normal, so periods may be heavy.
• Overweight: About 80% of affected women are overweight or obese.
• Blackening of the skin: black spots of skin can form in the folds of the body such as the neck, groin area and under the breasts.
Headaches: Hormonal changes can trigger headaches in some women.
What are the problems experienced by patients in the long term?
The hormonal disorder in Polycystic Ovary Syndrome causes multiple problems, the most important of which are:
• Infertility.
• Gestational diabetes or high blood pressure during pregnancy.
• Abortion or premature birth.
• Fatty hepatitis.
• Metabolic syndrome, where the patient complains of a group of problems including high blood pressure, increased blood sugar, and abnormalities in cholesterol and triglyceride levels that significantly increase the risk of cardiovascular disease.
• Type 2 diabetes or pre-diabetes.
• Sleep Apnea Syndrome.
• Depression, anxiety and eating disorders.
• Abnormal uterine bleeding.
• Endometrial cancer.

How is polycystic ovary syndrome diagnosed?
Doctors usually diagnose PCOS in women who have at least two of the following three symptoms:
• High androgen levels.
• Irregular menstrual cycles.
• Cysts in the ovaries.
Your doctor will ask about your symptoms and do a pelvic exam to look for any problems with the ovaries or other parts of the reproductive tract. The doctor will often need the following assistive examinations:
• Laboratory tests to determine the levels of male hormones.
• Laboratory tests to determine the level of cholesterol, insulin and triglycerides to assess the risk of heart disease and diabetes.
• Ultrasound scans to look for abnormal follicles and other problems in the ovaries and uterus.
What are the treatment steps?
Treatment for polycystic ovary syndrome usually begins with lifestyle changes such as weight loss, diet and exercise. Losing a few kilograms of body weight can help regulate your menstrual cycles and improve symptoms, improve cholesterol levels, reduce insulin, and reduce the risk of heart disease and diabetes.
Medications can help regulate your menstrual cycles and treat polycystic ovary symptoms such as hair growth and acne.
• Contraceptive pills: These pills restore the lost hormonal balance, regulate ovulation, and relieve symptoms. These hormones come in the form of pills, patches, or vaginal rings.
• Metformin: It is a medicine used to treat type 2 diabetes, and it also treats polycystic ovary syndrome by improving insulin levels.
• Clomiphene: It is a fertility drug that can help women with this condition get pregnant, but it increases the risk of a twin pregnancy.
• Surgery: Surgery may be an option for some patients if other treatments do not help.
From a cosmetic point of view, medications can be used to reduce hair growth, and hair can be removed either by traditional or laser methods.

the reviewer:

Premenstrual syndrome is a condition that affects a woman’s feelings, physical health, and behavior during several days of her menstrual cycle, usually just before her period. It is a very common condition, with symptoms affecting more than 90% of women, and it can disrupt some aspects of life. What are its causes, and how is it treated?
What are the causes of premenstrual syndrome?
It is not known exactly what causes Premenstrual Syndrome, but several factors are involved in this condition, including:
• Periodic changes in hormones: Symptoms and signs of premenstrual syndrome change with fluctuations in hormones, and disappear with pregnancy and menopause.
• Chemical changes in the brain: Serotonin is a brain chemical (neurotransmitter) believed to play a critical role in moods. Fluctuations in serotonin may trigger PMS symptoms. Inadequate amounts of serotonin can contribute to premenstrual depression as well as fatigue, food cravings, and sleep problems.
The incidence of premenstrual syndrome (PMS) increases if there is a psychiatric disorder such as depression, bipolar mood, or postpartum depression. It is also common in women who suffer from domestic violence, or emotional problems

 

What are the ways to treat premenstrual syndrome?
Premenstrual Syndrome cannot be cured, but you can take steps to relieve your symptoms. Treatment options if you have a mild to moderate form of PMS include:
• Drinking plenty of fluids helps relieve flatulence. Try to drink warm water and herbs, and avoid caffeinated drinks.
• Follow a balanced diet to improve your general health, by eating plenty of fruits and vegetables and reducing your consumption of sugar and salt.
• Take nutritional supplements such as folic acid, vitamin B-6, calcium, and magnesium to reduce colic and mood swings.
• Take vitamin D to reduce symptoms.
• Sleep for at least 8 hours during the night to relieve fatigue.
• Exercise can improve mood. Some women may prefer light and relaxing sports, such as yoga.
• Avoid smoking.
• Practicing hobbies helps in improving the mood.
For many women, lifestyle changes are enough to relieve PMS symptoms, but your doctor may prescribe one or more medications depending on the severity of your symptoms. Common PMS medications include:
• Antidepressants: These medications are the first line of treatment for premenstrual syndrome, especially in severe cases, or premenstrual depressive disorder. These medications are generally taken daily, but in some women with premenstrual syndrome, antidepressants are used only for the two weeks before menstruation begins.
• Non-steroidal anti-inflammatory drugs (NSAIDs): Taking non-steroidal anti-inflammatory drugs such as ibuprofen or naproxen sodium before or at the start of menstruation reduces cramping and discomfort in the breasts.
Diuretics: When exercise and reduced salt intake aren’t enough to reduce the weight gain, swelling and puffiness caused by PMS, taking diuretic pills may help your body get rid of extra fluid through the kidneys. Spironolactone (Aldactone) is a diuretic that helps relieve some of the symptoms of premenstrual syndrome.
• Hormonal contraceptives: These prescription medications stop ovulation, relieving PMS symptoms.

the reviewer:

Pregnancy is an important period in a woman’s life. The changes caused by pregnancy are reflected in the body and health of the pregnant mother. Some problems and disorders may appear that must be diagnosed and treated as early as possible to avoid complications that harm the health of the mother and the fetus.
Gestational diabetes is one of the common problems that affect pregnant women, which negatively affects the health of the fetus. In this article, we will learn about gestational diabetes, its causes, methods of diagnosis and treatment.
What is gestational diabetes?
In some women, blood sugar levels rise. This condition is known as gestational diabetes, and it usually occurs between 24 and 28 weeks of pregnancy.If you develop gestational diabetes, this does not mean that you had diabetes before pregnancy or that you will develop it after pregnancy, but it may increase the risk of developing type 2 diabetes in the future, and if it is not treated properly, it may raise the risk of your baby developing diabetes and increase the occurrence of complications for you and when Your baby during pregnancy and birth.
What are the symptoms of gestational diabetes?
Gestational diabetes may not cause any symptoms, and if you have some, they are often mild and include fatigue, blurred vision, extreme thirst and an urgent need to urinate. Therefore, doctors do not prefer to wait for symptoms to appear, but rather they investigate for high blood sugar between 24-28 weeks of pregnancy.

 

What are the causes of gestational diabetes?
The exact cause of gestational diabetes is unknown, but it is likely that hormones play a role. Hormones rise during pregnancy, which helps the placenta to grow and the pregnancy to continue, but it can also cause the body to become resistant to insulin.
When the body resists insulin, sugar rises abnormally, and this is called gestational diabetes.
What are the factors that increase your risk of gestational diabetes?
The incidence of gestational diabetes increases in pregnant women who have one of the following factors:

• A family history of diabetes.
• Gaining more weight than normal during pregnancy.
• Twin pregnancy.
The birth of a child weighing more than 4 kg previously
• Previous history of gestational diabetes.
• A story of an unexplained miscarriage or a stillbirth.
• Polycystic ovary syndrome (PCOS) or other conditions associated with insulin resistance.
How is gestational diabetes diagnosed?
If you do not have a known history of diabetes and your blood sugar levels are normal early in your pregnancy, your doctor will test for gestational diabetes often between 24-28 weeks of pregnancy.
Doctors order a glucose challenge test, where the pregnant woman is asked to drink a sugar solution and take a blood test one hour and two hours later. Higher numbers indicate gestational diabetes, if:
Fasting blood glucose greater than or equal to 92 mg/dL
• The blood sugar level after one hour is higher or equal to 180 mg/dL
• The blood glucose level after 2 hours is higher or equal to 153 mg/dL
It is important to remember that these numbers vary slightly from one laboratory to another.
What is the treatment plan that doctors follow when developing gestational diabetes?
The treatment plan depends on your blood sugar levels during the day. In most cases, your doctor will advise you to measure your blood sugar levels before and after meals, treat your condition by eating healthy food and exercising regularly, and may also add insulin injections if necessary.

It is important for a pregnant woman to learn how to use a blood sugar monitor and insulin injections, in order to be able to monitor sugar frequently during the day and adjust it. Ask your doctor about the correct way to time your insulin injections with your meals and exercises to avoid low blood sugar.
Is gestational diabetes dangerous?
If gestational diabetes is not well managed, blood sugar levels may remain higher than they should be during your pregnancy. These excess amounts of sugar pass from the mother’s blood through the placenta to the fetus, and the fetus makes more insulin.
Insulin causes an increase in the size of the fetus, which leads to difficulties in childbirth such as difficulty delivering shoulders, and brachial plexus paralysis. The doctor may resort to a cesarean section in order to avoid the impact of the large fetus in the birth canal. These children suffer from breathing difficulties, especially those who were born prematurely, and they also have an increase in the number of red blood cells, which leads to the occurrence of neonatal jaundice. In these children, high insulin causes a drop in blood sugar after birth, which leads to convulsions. Improperly treated gestational diabetes may result in the death of the baby during fetal life or shortly after birth. In the long run, children of mothers with diabetes are at risk of developing diabetes throughout their lives.
For the mother, gestational diabetes increases the risk of high blood pressure during pregnancy and pre-eclampsia, as well as the long-term risk of heart problems and diabetes.
Many of these complications can be avoided by strictly following the recommendations of the attending physician, and ensuring good control of sugar.

Can gestational diabetes be avoided?
Although there are no guarantees that gestational diabetes will not occur, following general health rules may be useful in reducing the risk of gestational diabetes and type 2 diabetes in the future, the most important of which are:
• Try to follow a healthy diet rich in vegetables, fruits and whole grains. Your diet should be rich in fiber and low in fat.
• Get rid of excess weight before pregnancy.
• Keep active. Exercising before and during pregnancy is beneficial. It is possible to do light sports such as walking for thirty minutes a day. Try to make this sport a daily part of your life, and remember its long-term benefits.

the reviewer:

After fertilization occurs, a zygote is formed, which is called fertilization. After several days, the fertilized egg reaches the uterine cavity and adheres to it. The implantation of the fertilized egg in the uterus or nesting is considered the beginning of pregnancy.
In some cases, the fertilized egg implants outside the main cavity of the uterus, a condition that we call ectopic pregnancy, and it is a dangerous situation and may threaten the life of the pregnant woman. So what is it? What are its symptoms and treatment methods?
What is pregnancy outside of the womb?
An ectopic pregnancy, also called an ectopic pregnancy, is the implantation of a fertilized egg outside the uterine cavity, and this often occurs in the fallopian tube that transports eggs from the ovary to the uterus, and this type of pregnancy is called a tubal pregnancy. An ectopic pregnancy can sometimes occur in other areas of the body such as the ovaries, the abdominal cavity, or the lower part of the uterus (cervix) that connects to the vagina. An ectopic pregnancy cannot continue normally, a fertilized egg cannot survive and the implanted tissue may cause life-threatening bleeding if left untreated.What are the causes of an ectopic pregnancy?
The cause of an ectopic pregnancy is not always clear, but studies indicate a number of factors that may play a role in its occurrence, the most important of which are: the shape and condition of the fallopian tubes, and various genetic and hormonal factors.
All women are exposed to an ectopic pregnancy, but the possibility of its occurrence increases in some women more than others, especially:• The mother’s age is 35 years or more.
• Previous pelvic or abdominal surgery.
• Previous infection with pelvic inflammatory disease.
• Previous endometriosis.
• Pregnancy with an intrauterine device (IUD).
• Pregnancy as a result of infertility treatment techniques.
• Smoking.
• Previous ectopic pregnancy.
• Previous infection with sexually transmitted diseases such as chlamydia and gonorrhea.
• The presence of structural abnormalities in the fallopian tubes that make it difficult for the fertilized egg to move towards the uterus.What are the symptoms of an ectopic pregnancy?
It is not possible to distinguish an ectopic pregnancy at first, the symptoms may start as any normal pregnancy, where the menstrual cycle occurs, the pregnancy analysis is positive, and nausea and vomiting may occur.
When a normal pregnancy grows, the uterus expands, while the fallopian tubes cannot stretch enough, and this expansion causes a group of symptoms, the most important of which are:• Sharp waves of pain in the abdomen, pelvis, shoulder or neck.
• Severe pain that appears on one side of the abdomen.
• Mild to severe vaginal bleeding or spotting.
• Dizziness or fainting.
Later, the fallopian tube may rupture due to its excessive stretching, and the rupture is considered a life-threatening emergency.
How is an ectopic pregnancy diagnosed?
Many women resort to a home pregnancy test to find out if they are pregnant, and this test gives a positive or negative result. While the laboratory analysis depends on the measurement of the hCG hormone, this hormone doubles every two or three days at the beginning of pregnancy, and continues to increase during pregnancy.
When this duplication does not occur, the hormone increases very slowly, and may not increase at all, which is what worries doctors. Of course, the failure of replication does not diagnose the presence of an ectopic pregnancy, but it is an indication of a problem, which may be an ectopic pregnancy, a failure to implant a fertilized egg, or an imminent miscarriage.
The next step in diagnosis is a transvaginal ultrasound, where the uterine cavity is empty, and the doctor may be able to see the gestational sac in the fallopian tubes if it is large enough. The doctor may ask to monitor the tests when the diagnosis is not certain.
If you have severe symptoms such as severe pain or bleeding, there may not be time to complete all of these steps. In these cases, an emergency operation is performed to avoid fallopian tube rupture and severe life-threatening bleeding.What are the ways to treat an ectopic pregnancy?
Ectopic pregnancy is not safe for the mother, and the fetus will not be able to reach maturity. It is necessary to remove the fetus as soon as possible to ensure the mother’s health now and her fertility in the long term. Treatment options vary depending on the location and degree of development of the ectopic pregnancy, and include:
• Medications: The drug option can be used in early cases, and methotrexate is the most common drug used. Methotrexate is a drug that stops the growth of rapidly dividing cells such as cells of an ectopic pregnancy. It is given by injection. Methotrexate is generally considered a safe drug, but it is severely teratogenic, so pregnancy should be avoided after taking it for several months.
• Laparoscopic surgery: Some cases of ectopic pregnancies are treated through laparoscopic surgery, where a small incision is made in the abdomen near or in the navel. Then the doctor uses a thin tube equipped with a camera and light (endoscope) to see the area of ​​the tube. An ectopic pregnancy can be removed and the tube left to heal on its own. But in some cases, the ectopic pregnancy and the tube must be removed together. Choosing one of these two methods depends on the amount of bleeding and damage, and whether the tube has ruptured or not. Another factor is the condition of the other tube, whether it is normal or shows signs of previous damage.

 

• Emergency surgery: If the ectopic pregnancy causes profuse bleeding, you may need emergency surgery, which can be done laparoscopically or through an abdominal incision (laparotomy). In some cases, the fallopian tube can be saved, but if the tube has ruptured, it must be removed.

the reviewer:

Breast cancer is the most common cancer that affects women, and fortunately, breast cancer is considered a treatable and curable disease, especially if it is diagnosed early. What is breast cancer? And why does it happen? What are the methods of treatment?
What is breast cancer?

 

Some cells in the breast can grow abnormally and form a lump. This is what we call breast cancer. Breast cancer occurs in the lobules or ducts of the breast. The lobules are the glands that secrete milk and the ducts are the passages that carry milk from the glands to the nipple, but cancer can occur in the fatty tissue or the elastic fibrous tissue inside the breast. Uncontrollable cancer cells often invade healthy breast tissue and travel to the lymph nodes under the arm. Lymph nodes are the primary pathway that helps cancer cells travel to other parts of the body.

What are the symptoms of breast cancer?
No woman should neglect any strange symptom that she feels in the breast, as breast cancer can cause a group of symptoms, the most important of which are: feeling a lump in the breast, secretions from the nipple other than milk, peeling in the skin of the nipple, withdrawal of the nipple inward, a lump or swelling under the arm A change in the shape, color, or size of the breast.
Why does breast cancer happen?
It is not clear why some people develop cancer while others do not. In fact, there is no specific reason for this, but there are a group of factors that increase the risk of infection, as breast cancer tends to occur in women after 55 years, especially those who have not given birth before, or They gave birth for the first time after the age of thirty.
Some hormonal, genetic and environmental factors play a role in the occurrence of cancer, the most important of which are:

• Early menstruation (before the age of 12 years), or late menopause (after 55 years).
• Hormone therapy: Taking estrogen and progesterone medications after menopause increases the risk of breast cancer.
• Having previously had ovarian, uterine or breast cancer.
• Obesity.
• Having a history of breast cancer in the family.
Despite all this, breast cancer may affect people who do not carry any risk factor, and it may affect men in some cases. Therefore, periodic examination and early detection are the basis for the success of treatment.
How is breast cancer diagnosed?
There are several tests and procedures used to diagnose breast cancer, including the following:
• Breast examination: Your doctor will examine both the breasts and the lymph nodes under the armpit, to check for any lumps or other abnormalities.
• Mammogram: It is an X-ray of the breast and is often used to check for breast cancer. If abnormalities appear on your mammogram, your doctor may recommend other procedures.
• Mammogram: It is used to determine whether a new breast lump is a solid mass or a fluid-filled cyst.
• Breast magnetic resonance imaging (MRI).
• Taking a sample of breast cells for testing (biopsy): It is the only way that can confirm the presence of breast cancer, as the cells taken from the tissue of the suspected area are sent to the laboratory to find out whether the cells are cancerous or not. It also determines the type of cells found in breast cancer, and whether the cancer cells contain hormone or other receptors.
There is also a set of tests and procedures used to determine the stage of breast cancer, including the following:
• Blood tests, such as a complete blood count.
• A mammogram of the other breast to look for signs of cancer.
• Breast magnetic resonance imaging (MRI).
• Bone scan.
• Computerized tomography (CT Scan).
• Positron emission tomography (PET Scan).
How is breast cancer treated?
Breast cancer has many treatment options, and the method is determined based on the type, degree and size of the cancer, the most important of which are:
• Surgery: There is more than one surgical method used, and the choice of method depends on the size of the tumor and the extent of its spread. These include lumpectomy, mastectomy, or excision of both breasts.
• During the operation, surgeons remove some lymph nodes and are examined. If they are infected, the lymph nodes must be removed as well.
• Radiation therapy.
• Chemotherapy: the use of drugs to kill cancer cells. Some people may undergo chemotherapy alone, but this type of treatment is often used in combination with other treatments, especially surgery.
• In some cases, doctors prefer to give patients chemotherapy before surgery, as they hope that the chemotherapy will shrink the tumor and then the surgery will be easier.
• Hormone therapy: It is used to treat types of breast cancer that are sensitive to hormones. Hormone therapy can help slow or even stop the growth of breast cancer.
• Medications.
• Supportive care: Patients need care and psychological support after the operation, as many of them feel dissatisfied with their appearance after the operation. Support from family and close friends is important, and attending support groups and meeting with cancer survivors can be helpful. These meetings provide information and advice about wig shops and special bras, which can reduce psychological distress.
What are the recommendations for breast cancer?

Cure rates for breast cancer are high if detected and treated early, while the chances of a cure are low if diagnosed late. Doctors recommend a periodic monthly examination after the end of the menstrual cycle, and the woman can conduct this examination on her own, as she is best able to detect any changes that occur in the structure and texture of the breast.
An annual examination should be conducted by an expert doctor, and a mammogram is performed once every two years after the age of forty, and once every year after the age of fifty.
Of course, any woman should seek medical advice as soon as she feels any change in the shape, texture or size of the breast, in order to ensure her safety.
the reviewer:

Cancer is the growth of cells that are abnormal and out of control. These cells can invade and destroy healthy tissue. The cancer is called the area from which it originated.
In this article, we will talk about cervical cancer, what are its causes? What are the ways to treat and prevent it?
What is cervical cancer?

 

Cervical cancer is a type of cancer that begins in the cervix, the tube that connects the lower part of a woman’s uterus to the vagina. Cervical cancer is a common occurrence in women, and its importance lies in the possibility of early detection and prevention of its occurrence.
What are the symptoms of cervical cancer?

Most women diagnosed with cervical cancer do not learn of the disease early, because it usually does not cause any symptoms until its later stages. When symptoms do appear, it is easy to confuse them with other conditions such as menstrual cycles and urinary tract infections.
• Abnormal bleeding, for example, between periods, after intercourse, or after menopause.
• Vaginal discharge that looks or smells different than usual.
• Pelvic pain.
• Increased need to urinate

What are the causes of cervical cancer?
The human papillomavirus (HPV), which is sexually transmitted, is the main cause of most cervical cancers. When you are exposed to this virus, the body’s immune system prevents the virus from causing harm in most cases, but the virus may sometimes survive and turn some cervical cells into cancerous cells.

Studies point to the human papillomavirus, as it causes various cancers in women and men, the most important of which are: vulvar cancer, vaginal cancer, penile cancer, anal and rectal cancer.

Who are the women who are eligible for infection?
Cervical cancer can affect any woman, and it can occur at a young age. However, there are a number of factors that can put a woman at risk, and increase her risk of infection, the most important of which are:
• Multiple sexual relations.
• Having a sexually transmitted disease such as human immunodeficiency virus (AIDS), chlamydia, or gonorrhea.
• Smoking.
• Obesity.
• Infection of the mother or sister with cervical cancer.
• Take birth control pills.
• Having more than three children, especially if the woman’s age at the time of her first child was young.
How is cervical cancer diagnosed?
Tests can be useful in detecting cervical cancer and pre-cancerous cells that may develop into cancer, the most important of which are:
Pap smear test: During the smear test, the doctor scrapes and brushes the cervical cells on a glass plate and then examines them in the laboratory for abnormalities. A smear test can identify abnormal cells in the neck, including cancer cells, or that show changes that increase the risk of cervical cancer.
• HPV DNA test: Cells collected from the cervix are checked for infection with any type of HPV that often causes cervical cancer.
If cervical cancer is suspected, your doctor will often start with a cervical exam, in which he uses a special magnifying instrument called a colposcope to look for any abnormal cells. During a colposcopy, your doctor takes a sample of cells from your neck (biopsy) for laboratory testing.
If the results of the initial biopsy are not reassuring, your doctor may order a biopsy under general anaesthesia, so that he or she can take a sample of your cervix large enough to make a definitive diagnosis.
If you are diagnosed with cancer, you should undergo additional tests to determine the extent (stage) of the cancer. The stage of the cancer is a major factor in determining treatment. These tests include:
• Imaging tests: Computerized tomography (CT scan), magnetic resonance imaging (MRI) and positron emission tomography (PET scan) help your doctor determine the presence of cancer spreading outside the cervix.
• Cystoscopy and rectum.
How is cervical cancer treated?
Cervical cancer is very easy to treat if caught early, and the four main treatments include:
• Surgery: The goal of surgery is to remove as much of the cancerous mass as possible. In the early stages of cancer, it may be sufficient to remove the area containing the cancerous cells. For more widespread cancer, surgery involves removing the neck and other organs in the pelvis.
• Radiation therapy: Radiation therapy kills cancer cells using high-energy rays, which can be delivered through a machine from outside the body or from inside the body using a metal tube placed in the uterus or vagina.
• Chemotherapy: which uses drugs to kill cancer cells throughout the body. Doctors give this treatment in the form of runs, where the patient is given chemotherapy for a period of time and then the treatment is stopped to give the body a chance to recover.
• Targeted therapy: bevacizumab (Avastin) is a new drug that works differently from chemotherapy and radiation, by preventing the growth of blood vessels that nourish cancer and help it grow and survive. This medication is often given with chemotherapy.
What are the ways to prevent cervical cancer?

Cervical cancer is one of the few preventable cancers, as a vaccine has been released to prevent infection with the human papilloma virus, which is the main factor in the occurrence of this cancer.
On the other hand, early detection of cervical cancer can be done through a smear procedure, which is an easy procedure that is carried out in the clinic. A Pap smear can reveal the presence of cell changes or abnormal cells, and it can detect the presence of cancer in its early stages where it is still easy to treat. Early detection programs recommend a Pap smear every two years.

the reviewer:

The uterus is a hollow, pear-shaped organ located in the pelvis and is the place where the fetus grows. The lining of the uterus sheds and is renewed monthly, and the lining cells grow and multiply to replace the lost cells. In some cases, this growth is disturbed, leading to the appearance of abnormal cells, or the so-called cancerous cells.

 

Endometrial cancer affects the layer of cells that make up the uterine lining, and is sometimes called uterine cancer. Other types of cancer can form in the muscle of the uterus, but they are much less common than endometrial cancer. Endometrial cancer is often diagnosed in the early stages, because it often causes vaginal bleeding, and if detected early, surgical removal of the uterus is often curative.

What are the symptoms of endometrial cancer?
The most common symptom of endometrial cancer is abnormal vaginal bleeding, and this includes the following:
• Changes in the length and intensity of the menstrual cycle.
• Vaginal bleeding or spotting between periods.
• Postmenopausal bleeding.
• Vaginal discharge that is watery or contains little blood.
• Pain in the lower abdomen or pelvis.
• Pain during intercourse.
Who are the women at risk of developing endometrial cancer?
The risk of developing uterine cancer increases with age. Most cases of cancer are diagnosed after the age of 45. Other factors include:
• Some diseases such as diabetes mellitus.
• Family history of endometrial cancer.
• Previous breast or ovarian cancer.
• Hypertension.
• The pelvic area was previously exposed to radiation.
• Changes in the balance of female hormones: the ovaries secrete two hormones, estrogen and progesterone. If the balance of these two hormones changes so that it shifts in the direction of increased estrogen, this will increase the risk of developing endometrial cancer, and this occurs in the following cases:
• Menstrual years: The more menstrual cycles you have during your lifetime, the greater your body’s exposure to estrogen. If your first period was before the age of 12 or you went through menopause later in life, your risk of uterine cancer increases.
• History of pregnancy: During pregnancy, the hormonal balance changes towards an increase in progesterone, so endometrial cancer commonly affects women who have not given birth, unlike cervical cancer, which is more frequent in women who have given birth to more children.
• Polycystic Ovary Syndrome (PCOS): In this disease, estrogen levels are high and progesterone levels are usually low, which increases the chances of developing endometrial cancer.
• Obesity: Excess weight increases the risk of endometrial cancer because excess fat alters the balance of hormones in the body.
Some types of medications can also alter the balance of estrogen and progesterone in the body, including:
• Hormone therapy for breast cancer can increase the risk of endometrial cancer.
• Estrogen replacement therapy used to treat menopausal symptoms increases the risk of endometrial cancer.
How is endometrial cancer diagnosed?
Your doctor will ask about your symptoms and medical history, perform a pelvic exam to see and feel for abnormalities in your uterus and other reproductive organs, and may order a transvaginal ultrasound. If the doctor identifies any changes during the ultrasound examination, he or she will order one or more of the following tests to collect a sample of tissue for examination:
• Endometrial biopsy: In this test, your doctor inserts a thin, flexible tube into the uterus to take a small piece of endometrial tissue through the tube.
• Hysteroscopy: In this examination, the doctor inserts a thin, flexible tube with a camera at the end of it into the uterus through the cervix. He uses this endoscope to visually examine the lining of your uterus and take biopsies for existing abnormalities.
• Dilation and curettage: If the biopsy samples are not clear, the doctor may collect another sample of endometrial tissue by scraping and dilation, where he dilates the cervix and uses a special instrument to scrape the tissue from the lining of the uterus.
After collecting the tissue sample, it is sent to the laboratory to see if it contains cancerous cells. If it is confirmed that you have endometrial cancer, your doctor will often order other tests to see if the cancer has spread, such as blood tests, X-rays, CT scans of the abdomen, and others. from imaging examinations.
What are the ways to treat endometrial cancer?
Treatment options for endometrial cancer include:
• Surgery: Surgery is the best option. Surgeons remove the uterus, and the ovaries and fallopian tubes may also be removed. In some cases, surgery involves removing nearby lymph nodes if there is a suspicion that they are infected. In the early stages of endometrial cancer, surgery is considered completely curative.
• Radiation therapy: Radiation therapy uses high-energy beams to kill cancer cells. Radiation therapy can be applied from outside the body, or by placing radioactive materials in the uterus or vagina.
• Chemotherapy: Chemotherapy uses drugs to kill cancer cells. The drugs may be in pill form or given intravenously.
• Hormone therapy: Hormone therapy works to change the levels of hormones in the body, which slows down the growth of cancer cells. The doctor may suggest hormonal treatment for advanced stages of cancer, or if the cancer has returned after treatment, and it is often combined with chemotherapy.

The C125 antigen test, which is one of the tumor markers, can be performed in many cases, one of which is endometrial cancer, and this antigen is elevated in the laboratory, so it cannot be relied upon to make the diagnosis. On the other hand, it is considered a good examination to follow the progress of treatment and relapse, if it occurs.

the reviewer:

The body’s cells are in constant motion, dividing and multiplying to replace damaged and lost cells. When the body loses control over its own cells, these cells begin to multiply pathologically, forming a tumor mass.
Cancer may affect any member of the female reproductive system, some of them show early symptoms, while others are delayed in diagnosis. Unfortunately, the symptoms of ovarian cancer are delayed, making treatment difficult.

 

What are the symptoms of ovarian cancer?
It is easy to overlook the early symptoms of ovarian cancer because they are similar to other common diseases or because they tend to come and go, and they include the following: a feeling of bloating and abdominal pain, a feeling of early fullness, and an increased frequency of urination.

Later, as the disease progresses, other more obvious symptoms begin to appear, including:
• Digestive symptoms such as indigestion, constipation, and heartburn.
• Symptoms related to hormonal disturbances, such as menstrual irregularities, or bleeding after menopause.
• Low back pain.
• Painful intercourse.
• Dermatomyositis (a rare inflammatory disease that can cause skin rashes, muscle weakness and sore muscles)
Unfortunately, most of these symptoms are associated with many causes, and they often go away with simple treatments such as painkillers. As the tumor grows, the symptoms will recur more severely, prompting the patient to see a doctor, and then the cancer will most likely have spread outside the ovary, making it more difficult to treat effectively.
Why does ovarian cancer occur?
The exact cause of ovarian cancer is unknown, but some factors may increase your risk:
• Family history of ovarian cancer, in fact less than 5% of ovarian cancer is linked to genetic conditions, but you should be careful if your mother, sister or daughter has had ovarian cancer previously.
• A personal history of breast cancer, uterine cancer or colon cancer.
• Obesity.
• The use of some fertility drugs or hormonal treatment that contain estrogen.
• Absence of a previous pregnancy story.
• Endometriosis.
• Age. Ovarian cancer tends to occur in women after menopause, and it rarely affects young women.
How is ovarian cancer diagnosed?
If your doctor suspects you have ovarian cancer, he or she will likely recommend a pelvic exam. A pelvic exam can help your doctor detect abnormalities, but small ovarian tumors can be very difficult to feel.
The doctor may also perform the following tests:
• Transvaginal ultrasound: It is used to detect tumors in the reproductive organs, including the ovaries, but it cannot determine whether these masses are healthy or cancerous.
• Computerized tomography of the abdomen and pelvis (CT Scan) can show tumors and masses well, and some doctors may use magnetic resonance imaging (MRI) instead.
• Blood tests to measure the levels of carcinomatous antigen 125 (CA-125): It is a tumor marker that is found in high quantities in the blood of a woman with ovarian cancer, and gives an indication of the possibility of infection. In many other conditions, C125 is elevated, so it is not high enough to make a diagnosis, but it is widely used to assess response to treatment in ovarian and other reproductive cancers.
• Biopsy: This is the only way your doctor can confirm that you have ovarian cancer and determine the type of cancer cells.
After making the diagnosis, the doctor may order a chest x-ray to assess the spread of the tumor to the lungs, and laparoscopy is useful to know its spread within the abdominal cavity.
What are the ways to treat ovarian cancer?
Treatment depends on how far the tumor has spread. The treatment plan includes one or two of the following:
• Surgery: Surgery is the main treatment for ovarian cancer. The aim is to remove the tumor, but it is often necessary to remove the entire uterus. The doctor may also recommend removing both the ovaries, fallopian tubes, nearby lymph nodes, and other pelvic tissues, to ensure that no cancerous cells are left in the abdomen.
• Chemotherapy: Chemotherapy is often used after surgery to kill any remaining cancer cells.
• Modern treatments such as hormonal therapy that inhibits tumor growth, and targeted therapy that reduces tumor perfusion and prevents its nutrition while causing minimal damage to healthy cells in the body.

Are there methods for early detection of ovarian cancer?
It is much easier to treat ovarian cancer when it is diagnosed in the early stages, but it is not easy to detect it early, as the ovaries are located deep within the abdominal cavity, so it is not easy to feel the presence of a tumor, and its symptoms are very similar to many common diseases.
There’s no routine diagnostic test for ovarian cancer, and cervical smears aren’t helpful in detecting ovarian cancer, so it’s important to tell your doctor about any frequent or unusual symptoms.

the reviewer:

Articles of Diseases : Bone and muscle diseases

Articles of Diseases

جراحة استبدال المفاصل هي إزالة جزء أو كل المفصل التالف وتركيب مفصل صناعي ليسمح للطرف بالتحرك بحرية دون ألم أو قيود. عادةً ما يكون المفصل الاصطناعي مصنوعًا من البلاستيك، أو المعدن، أو السيراميك، أو مزيج من هذه المواد. يتم إجراء معظم عمليات استبدال المفاصل تحت التخدير العام أو الموضعي.
هناك سببان رئيسيان لاستبدال المفاصل: الأول هو تخفيف الألم، فخلال عملية استبدال المفصل يقوم الجراح بإزالة الأسطح التالفة من المفصل واستبدالها بزراعات صناعية بديلة مما يؤدي إلى التخلص من الألم، والسبب الثاني هو تحسين نوعية الحياة وقدرة المريض على القيام بالعمل، فبعد تركيب المفصل الجديد يستطيع العديد من الأشخاص المشي بسهولة أكبر وقد يتمكن البعض من ركوب الدراجة وممارسة الرياضات المختلفة، وسنتحدث هنا عن الركبة و تعتبر عمليات استبدال مفصل الورك من أكثر العمليات الجراحية شيوعاً في هذا المجال.
ما هو استبدال مفصل الركبة؟
يعد الضرر الناجم عن التهاب المفاصل هو السبب الأكثر شيوعًا لاستبدال مفصل الركبة، وهذا يشمل كلاً من هشاشة العظام والتهاب المفاصل الروماتويدي. عادة ما تستغرق عملية إزالة مفصل الركبة واستبداله بمفصل صناعي جديد أقل من ساعتين، ولكن تعود الحياة إلى طبيعتها وقد تستمر عملية إعادة تأهيل المفصل لعدة أشهر.
تعتبر عملية استبدال مفصل الركبة من العمليات الجراحية الشائعة نسبياً، وهي عملية فعالة للغاية حيث يتمكن معظم المرضى من العودة إلى حياتهم الطبيعية وممارسة العديد من الأنشطة، لكن الأطباء ينصحون بتجربة علاجات أخرى مثل: فقدان الوزن، والأدوية، والعلاج الطبيعي، استخدام أدوات مساعدة المشي كالعكاز والعكاز قبل اللجوء إلى تبديل المفصل.
من المهم أن نتذكر أن حالة كل مريض تختلف عن الأخرى، فشدة الألم ومدى تداخله مع الأنشطة اليومية مثل المشي وصعود السلالم، ومدى الإعاقة التي يسببها، وإذا كانت الركبة مشوهة ومنحنية، و الحالة الصحية للمريض، هل كان قادراً على تحمل العملية أم لا.
ما هو الغرض من استبدال مفصل الورك؟
الحالات التي يمكن أن تلحق الضرر بمفصل الورك وتتطلب إجراء عملية جراحية لاستبدال المفصل بمفصل صناعي تشمل العديد من الحالات مثل: التهاب المفاصل الروماتويدي الذي يسبب تآكل الغضاريف والعظام مما يؤدي إلى تشوه المفصل، موت العظام الذي يحدث بسبب عدم كفاية الدم وصولاً إلى مفصل الورك، مما يؤدي إلى خلعه أو كسره، مما يؤدي في النهاية إلى انهيار المفصل وتشوهه.
يلجأ الأطباء في البداية إلى المسكنات ومضادات الالتهاب غير الستيروئيدية والعلاج الطبيعي ومجموعة من التوصيات لتخفيف الضغط على المفصل التالف. لكن مع مرور الوقت تزداد الإصابة ويصبح الألم شديدا ومستمرا، ولا يستجيب للمسكنات، مما يعيق الحركة، فيصبح المشي صعبا حتى لو استخدم المريض العصا والعكاز. ويؤثر ذلك أيضًا على قدرة المريض على صعود ونزول الدرج، والنهوض من وضعية الجلوس. الأنشطة اليومية البسيطة مثل ارتداء الملابس صعبة.
كيف تستعد لاستبدال المفصل؟
قبل العملية يقوم جراح العظام بإجراء فحص للمريض، من خلال السؤال عن التاريخ الطبي وإذا كان المريض يعاني من أمراض معينة والسؤال عن الأدوية التي يتناولها، ثم يقوم بفحص المفصل مع الاهتمام بمدى الحركة والقوة للعضلات المحيطة، ومن ثم يطلب إجراء اختبارات الدم والأشعة السينية للمفصل، وقد يحتاج المريض إلى تقييم أكثر دقة مثل التصوير المقطعي المحوسب (CT) أو التصوير بالرنين المغناطيسي (MRI).
نظرًا لأن التدخين يمكن أن يتعارض مع العلاج، فمن المهم التوقف عن استخدام منتجات التبغ لمدة شهر على الأقل قبل الجراحة ولمدة شهرين على الأقل بعد الجراحة، وإذا كان من الصعب التوقف عن التدخين، تحدث مع طبيبك للحصول على المساعدة.
ماذا يحدث أثناء استبدال مفصل الركبة؟
تستمر العملية الجراحية ما بين ساعة إلى ساعتين وتتم تحت التخدير العام أو الموضعي في غرفة العمليات بالمستشفى، حيث يقوم الجراح بعمل شق جراحي فوق الركبة وإزالة الجلد والعضلات ومن ثم إزالة العظام التالفة والمتضررة و الغضروف، ومن ثم تثبيت مفصل الركبة الجديد على عظمة الفخذ وعظم الساق باستخدام دبابيس ومسامير اسمنتية متخصصة، ومن ثم يقوم الجراح بإغلاق الجرح بالغرز ووضع الضمادة المناسبة.
ماذا يحدث أثناء عملية استبدال مفصل الورك؟
تستغرق هذه الجراحة بضع ساعات تحت التخدير العام أو الموضعي، حيث يقوم الجراح بعمل شق في مقدمة أو جانب الورك من خلال طبقات الأنسجة المختلفة ثم يقوم بإزالة العظام والغضاريف التالفة ويترك العظام السليمة في مكانها، و ثم يتم استبدال الكرة المستديرة الموجودة أعلى عظمة الفخذ بالكرة الصناعية، ويتم زرع مقبس صناعي في عظمة الحوض ليحل محل السنخ التالف.
بعد العملية ماذا سيحدث؟
بعد الجراحة يجب البقاء في المستشفى لعدة أيام حتى يتم التأكد من الشفاء التام. سيقوم الفريق الطبي بمراقبة الضغط والنبض والتأكد من تناول الأدوية في الوقت المناسب. تساعد المسكنات في السيطرة على الألم والوجع الذي يشعر به المريض بعد الجراحة، ويحتاج العديد من المرضى إلى تلقي جرعات من الأدوية لمنع تجلط الدم ومنع تكون جلطات الدم.
يشجع الأطباء المرضى على المشي مبكراً، حتى لو كان مؤلماً، لتحريك مفاصل وعضلات الجسم، وقد يحتاج المريض إلى تناول مسكنات الألم للسيطرة على الألم خلال الأيام الأولى. لاحقًا، يعد العلاج الطبيعي مهمًا جدًا لسرعة الشفاء وتقوية العضلات وتحريك المفاصل، وسيساعد المعالج الطبيعي المريض على تعلم كيفية استخدام العكازات وأدوات المشي المختلفة.

المراجع:

التهاب المفاصل الروماتويدي هو مرض مناعي ذاتي تقدمي طويل الأمد يسبب التهابًا وتورمًا وألمًا في المفاصل وأجزاء أخرى من الجسم. يعد التهاب المفاصل الروماتويدي مرضًا شائعًا إلى حد ما، حيث يصيب حوالي 1٪ من سكان العالم. ما هو التهاب المفاصل الروماتويدي وما هي طرق علاجه؟

ما هو التهاب المفاصل الروماتويدي؟
التهاب المفاصل الروماتويدي هو أحد أمراض المناعة الذاتية وكذلك مرض جهازي، مما يعني أنه يؤثر على الجسم كله. للحصول على جسم سليم وسليم، يقوم جهاز المناعة بمهاجمة الخلايا والجراثيم الضارة والغريبة، ولكن في بعض الأحيان يبدأ جهاز المناعة بمهاجمة أنسجة وأعضاء الجسم عن طريق الخطأ لاعتقاده أنها أجسام غريبة وضارة. في هذه الحالة، يتسبب الجهاز المناعي في تدمير الأنسجة والأعضاء السليمة، وفي حالة التهاب المفاصل الروماتويدي، يمكن أن تكون هذه الأنسجة المفاصل، أو الرئتين، أو العينين، أو القلب.

ما هي أعراض التهاب المفاصل الروماتويدي؟
التهاب المفاصل الروماتويدي هو مرض مزمن تتأثر فيه مجموعة من المفاصل في وقت واحد، وغالباً ما تشمل هذه المفاصل مفاصل اليدين والقدمين، وتشمل الإصابة نفس المفاصل في جانبي الجسم، وهذا ما يميزه عن بعض الأمراض التي تؤثر على مفصل واحد، مثل التهاب المفاصل الإنتاني، على سبيل المثال. يتميز التهاب المفاصل الروماتويدي بنوباته المتكررة، حيث تتفاقم أعراضه وعلاماته خلال فترات معينة، ويفصل بين هذه الفترات أوقات قد تختفي فيها الأعراض تمامًا.

أعراض التهاب المفاصل الروماتويدي ليست صارخة في البداية. قد يشكو المريض من تصلب المفاصل، ويكون هذا التيبس في الصباح أو يحدث بعد الراحة أو الجلوس لفترة طويلة، ويختفي بعد تحريك المفاصل. وغالباً ما يؤثر التيبس على مفاصل اليدين ثم ينتقل إلى مفاصل أخرى. ويعاني بعض الأشخاص أيضًا من ارتفاع طفيف في درجة الحرارة، مع شعور بالتعب والضيق العام وشعور غامض بأنهم ليسوا على ما يرام. وتشمل الأعراض الأكثر شيوعاً ما يلي:
• آلام المفاصل، حيث تكون مفاصل الأصابع والمعصمين مؤلمة، خاصة عند الحركة. وفي وقت لاحق، يمكن أن تتأثر المفاصل الكبيرة مثل الركبتين والكتفين وغيرها، ويمكن أن تنتفخ هذه المفاصل وتصبح حمراء ودافئة.
• تصلب المفاصل، حيث يؤدي المرض إلى إصابة الأوتار، فلا يتمكن المريض من مد المفصل أو ثنيه بشكل كامل، وتتفاقم الحالة بسبب الألم الذي يشعر به المريض عند الحركة. قد يشكو بعض المرضى من عدم استقرار المفصل مما يعرضهم للخلع.
• قد يسمع المريض أصوات طقطقة عند تحريك مفاصل اليدين والقدمين، وهذا نتيجة اصطدام العظام الصغيرة ببعضها بسبب تلف الغضاريف الواقية.
تكون المفاصل طبيعية في البداية، ولكن فيما بعد مع تقدم المرض تتشوه هذه المفاصل.
وفي حوالي نصف الحالات يؤثر المرض على أعضاء أخرى في الجسم، مما يسبب جفاف الفم والتهاب العينين، وقد تتأثر الرئتان أو القلب أو الكلى أو الأوعية الدموية.

How is rheumatoid arthritis diagnosed?
Doctors usually pay attention to the details of symptoms, their severity, and when they occur. They also perform a clinical examination that includes examining the joints of the body for swelling and redness, checking range of motion, and testing reflexes, responses, and muscle strength. If your doctor suspects rheumatoid arthritis, he or she will likely refer you to a rheumatologist.

Since no single test can confirm a diagnosis of rheumatoid arthritis, a rheumatologist may use multiple tests such as a blood test for ANA antibodies often found in autoimmune diseases, or checking the level of certain substances that are elevated during inflammatory conditions. Other tests, such as the rheumatoid factor test, can also be done.
Doctors often order some radiological images, such as ultrasound, X-ray, or magnetic resonance imaging (MRI) to confirm the diagnosis and show the extent of damage or damage to the joints.

How is rheumatoid arthritis treated?
Medications available to treat rheumatoid arthritis include NSAIDs to treat inflammation and relieve pain, cortisone therapy, immunosuppressive therapy, and biological therapies. Although surgery is not considered the main treatment for rheumatoid arthritis, it may be necessary in some cases, such as excision of tendon repair or replacement of a severely damaged joint.

Doctors recommend constantly moving the joints to keep them supple and avoid joint deformities. Relaxation exercises or alternating warm and cold compresses can help lubricate the muscles and keep the joint moving. However, some aids may be necessary to avoid putting pressure on the affected joints.
What are the possible complications of rheumatoid arthritis?
People with rheumatoid arthritis are at risk of developing many diseases and complications. Some of these complications are related to the disease itself, while some are related to medications used to treat arthritis, including:
• Obesity, where the patients’ body mass index (BMI) increases significantly, and these people are at risk of developing diabetes and high blood pressure.
Carpal Tunnel Syndrome: It is a type of nerve damage that results from compression and irritation of the nerve in the wrist, and its symptoms include pain, numbness, tingling and tingling in the fingers, thumb and part of the palm.
• Inflammation: Inflammation can affect the lungs, heart, blood vessels, eyes, or other parts of the body.
• Tendon rupture: Inflammation in the tendons can rupture, especially on the back of the fingers.
• Inflammation of the blood vessels: Inflammation of the blood vessels can cause them to weaken, thicken and narrow, and this may affect blood flow to different tissues.
• Increased susceptibility to infection: There is a greater risk of catching colds, flu, pneumonia and many other diseases, especially if the affected person is taking immunosuppressive drugs to treat rheumatoid arthritis.
• Osteoporosis: It is a common disease in patients with rheumatoid arthritis, and cortisone treatment increases the exacerbation of osteoporosis.
• The secretions of the salivary and tear glands decrease, and the eyes and mouth become dry, which is known as Sjögren’s syndrome.
• Heart problems, where the risk of hardening and blockage of the arteries, which leads to heart attacks, increases, and the possibility of pericarditis increases.
• Lung disease: People with rheumatoid arthritis have an increased risk of inflammation and scarring of lung tissue, which can lead to lung cirrhosis and bronchiectasis. The membrane surrounding the lungs also becomes inflamed, leading to inflammation and effusion of the pleura.

the reviewer:

It is an infection of the joint, and may also be referred to as purulent arthritis. Septic arthritis usually occurs in only one joint, and the condition usually affects a large joint such as the knee, hip or shoulder, and occurs more often in children, the elderly, and people who use illegal drugs.
What are the symptoms of septic arthritis?
Symptoms of septic arthritis can vary, depending on the person’s age and the medications the person is taking. Symptoms may include:
• Severe pain that increases with movement.
• joint swelling.
• Hotness and redness around the joint.
• Fever.
• goosebumps.
• exhaustion.
• Lack of appetite.
• Rapid heart rate.
• irritation.
What are the causes of septic arthritis?
This inflammation occurs when infection caused by pathogens spreads to the joint or the fluid surrounding the joint called synovial fluid. The infection usually begins in another area of ​​the body and spreads through the bloodstream to the tissues of the joint. The infection may also enter the body through surgery, open wounds, or injections.
Septic arthritis occurs as a result of infection of the joint with a virus such as hepatitis A, hepatitis B, mumps, AIDS, and others, or bacteria such as streptococci, staphylococcus, and the latter being responsible for infection with gonorrhea. While the infection of the fungus occurs infrequently, and most often it affects the immunocompromised patients.
What are risk factors for septic arthritis?
Although septic arthritis is a condition that can affect anyone, it tends to affect some people more than others, including:
• The presence of joint problems such as osteomyelitis, gout, lupus, or rheumatoid arthritis.
• Having a history of joint surgery such as joint replacement surgery.
• The presence of certain skin conditions.
• The presence of open wounds.
• Drug or alcohol abuse.
• Taking medications that suppress the immune system, such as cortisone or chemotherapy for tumors.
• Weak immune system, such as patients with diabetes, liver failure, kidney failure, or AIDS.
• Cancer.
• Smoking.
• Diabetes.
How is septic arthritis diagnosed?
The doctor examines the joint and asks questions about the patient’s symptoms. If he suspects septic arthritis, he may order additional tests such as:
• Blood tests such as a complete blood count (CBC), which measures the number of red and white blood cells and platelets and can assess the presence of anemia or infection. Doctors also resort to other analyzes such as blood culture to see if bacteria are present in the bloodstream and determine their type.
• Arthrocentesis, where a sample of the inflamed joint fluid is taken and sent to the laboratory for examination in terms of color, viscosity, and the presence of white blood cells and bacteria. Test results can tell your doctor if a joint infection is present and what is causing the infection.
• Radiological examinations, including X-ray imaging, magnetic resonance imaging (MRI), computerized tomography (CT scan), and positron emission tomography (PET Scan).
How is septic arthritis treated?
Treatment for septic arthritis caused by bacteria usually begins with antibiotics to kill the bacteria causing the infection. The type of antibiotic used is determined based on the results of blood culture and joint fluid analysis. Sepsis must be treated quickly and aggressively to prevent degenerative arthritis and joint damage. As a result, doctors prefer to administer intravenous antibiotics, as they treat sepsis faster than oral antibiotics. Most people begin to feel better within 48 hours of treatment with antibiotics. Later, the patient completes the course of treatment with oral antibiotics, and most patients need a long treatment ranging from six to eight weeks. Your doctor may also prescribe antifungal medications instead of antibiotics if fungi are causing the infection, but viral arthritis doesn’t require any special treatment.
Many people with septic arthritis need draining the synovial fluid. This is done in order to reduce the amount of fluid within the joint, reduce pain and swelling, and prevent joint damage from worsening. This can be done by arthrocentesis (the removal of fluid with a needle), arthroscopy, or the surgical method. traditional. During an arthroscopy, your doctor will make several small incisions near the affected joint. Next, he will insert a small tube containing a camera into the incision. Usually, the doctor will insert a tube into the affected joint in order to prevent the joint from swelling again. The tube can be removed after several days.
Other treatment methods may be used to reduce pain along with treating sepsis. These methods include:
• Use of non-steroidal anti-inflammatory drugs.
• Rest the joint.
• Splinting the affected joint.
• the physical treatment.
the reviewer:

 

Most head injuries involve minor injuries that do not require specialized care or hospitalization, however they can cause chronic symptoms such as headaches or difficulty concentrating, and we may have to spend time away from many normal activities to get enough rest to ensure full recovery. But some head injuries can be severe and cause severe consequences, so head trauma should always be treated with caution.

What are head injuries?
Head injuries include any type of injury to the brain, skull, or scalp, and this can range from a mild bump or bruise to a brain injury.
Head injuries may be closed or open. A closed head injury is any injury that does not break the skull. An open head injury is an injury that penetrates the scalp and skull and reaches the brain, such as an open fracture or a gunshot. Consequences and treatments can vary greatly depending on the cause and severity of the head injury.

What are the types of head injuries?
There are many reasons that can cause head injury, in some cases the blow is as light as falling a few steps away, but it is enough to cause a problem in the brain structures. Head injuries include scalp wounds, facial and skull fractures, concussion, bruising and swelling of brain structures, and intracranial hemorrhage.

Concussion occurs in the brain when the trauma to the head is sufficient to injure the brain, and it is believed that it is the result of the brain hitting the hard walls of the skull. Minor injuries recur, causing severe injury.

In severe cases, some cerebral vessels rupture, causing bleeding inside the skull. The bleeding blood may collect between the brain and the bones of the skull, and bleeding may occur within the brain tissue, which is called cerebral hemorrhage. This bleeding causes damage to the nerve tissues, and the swelling of the brain and the accumulated blood causes a rise in pressure inside the skull, which exacerbates the nerve damage that occurs.

What are the symptoms of a head injury?
Symptoms of brain damage may be delayed for several days, and it is very important for the patient to be aware of the possible symptoms so that he can monitor their occurrence and tell the doctor, and these symptoms include: mild mental confusion, headache, difficulty concentrating, sleep disturbance, ringing in the ears and in some cases The only symptom may be a bump on the head, but the bump or bruise may be delayed for about 24 hours.

Symptoms of a more serious head injury that require special treatment include: a fracture of the skull or face, inability to move a limb, problems with balance, double vision, blurry vision, loss of consciousness or coma, persistent vomiting, seizures, inability to Moving eyes, etc.

Severe bruises in the head, especially those caused by car accidents, are accompanied by abdominal bruises and spinal bruises, and then it is important not to move the patient, call an ambulance immediately and make sure that the patient is able to breathe, and in the event of bleeding, pressing hard with a clean cloth on the wound To control blood loss.

How are head injuries diagnosed?
The first way to assess consciousness and potential head injury is the Glasgow Consciousness Scale. It is a 15-point test that assesses a patient’s mental state. A higher score on the scale indicates a less severe injury. Doctors use this scale to monitor progression over the days following the injury.

The doctor will need to know the circumstances of the injury, but often the patient will not remember the details of the accident. Therefore, doctors prefer talking to someone else who was present at the time of the accident to get some details if possible.

Imaging tests are often used to diagnose head injuries. A CT scan or magnetic resonance imaging (MRI) scan helps look for fractures, hemorrhages and brain swelling.

How are head injuries treated?
The treatment of head injuries depends on the type of injury. For patients with minor head injuries, monitoring is sufficient. The patient may need to take pain relievers to control the headache. It is preferable to avoid taking NSAIDs such as ibuprofen or aspirin because they increase bleeding if present. Take anti-nausea and anti-vomiting medications to relieve the patient’s sense of annoying nausea. If the patient has an open wound, the doctor may use sutures to close it and then cover it with a bandage.

In severe cases, the patient needs to be treated with anticonvulsants, and giving diuretics in order to increase fluid excretion and reduce high pressure inside the skull. A surgical procedure with the aim of draining the blood pool and thus relieving pressure on the brain tissue.

In the long run, minor injuries leave little trace, but severe injuries can cause permanent damage. These patients need physical therapy for a long time, and they may need to use assistive devices such as crutches and others.

How can head injuries be prevented?
Important safety measures include: not allowing children to play sports that are not appropriate for their age, supervising and teaching children how to use sports equipment properly, wearing a helmet to protect the head when riding a motorcycle, and wearing a seat belt when driving.

the reviewer:

Carpal Tunnel Syndrome is one of the common and increasing health problems in the current era, and it may sometimes be a minor and transient problem, but at other times it needs surgical and therapeutic intervention.
What is carpal tunnel syndrome?

It is a medical condition in which the median nerve, which runs from the middle of the arm to the palm of the hand, is compressed. This compression occurs in the wrist area, through which the median nerve passes on its way to the hand. The function of the median nerve is to transmit tactile sensations from the palm of the hand to the thumb, index finger, middle finger and part of the ring finger, in addition to controlling the work of some small muscles in the hand.

What are the causes of Carpal Tunnel Syndrome?
A combination of factors can compress or irritate the median nerve in the area where it crosses the carpal tunnel and cause carpal tunnel syndrome. For example, a broken carpal bone may narrow the carpal tunnel and irritate the median nerve, and rheumatoid arthritis may cause this syndrome due to the inflammation and swelling. In any case, there is no clear cause in most cases, and there may be a role for several combined factors that lead to the emergence of this syndrome, as a group of risk factors that increase the likelihood of developing this syndrome have been identified:
• Gender: Women are generally more prone to carpal tunnel syndrome, and this may be due to the small size of their carpal tunnel.
• Autoimmune diseases: Autoimmune diseases are a wide range of diseases that are associated with inflammatory conditions, as is the case in rheumatoid arthritis, which may affect the carpal tunnel, causing compression of the median nerve and the emergence of the syndrome.
• Nerve-damaging diseases: Some chronic diseases, especially diabetes, increase the risk of nerve damage, including damage to the median nerve.
• Fluid retention in the body, which frequently occurs during pregnancy and after menopause, leads to an increase in pressure within the carpal tunnel and irritation of the median nerve. It is noted that the symptoms of carpal tunnel syndrome associated with pregnancy improve after pregnancy.
• Other diseases such as high arterial pressure, chronic kidney failure, and thyroid disease.
This syndrome may also result from the use of some types of medications, such as anastrozole used in the treatment of breast cancer. The risk of carpal tunnel syndrome increases among obese people, smokers and people who do not engage in sufficient physical activity, and the incidence of infection increases in people who practice specific professions such as sewing.

What are the symptoms of Carpal Tunnel Syndrome?
Carpal tunnel syndrome usually presents with a feeling of tingling and numbness in the areas of the median nerve distribution in the hand, ie the thumb, index finger, middle finger and half of the ring finger, while the pinky is healthy. These symptoms are intensified at night and may even awaken the patient from sleep, and the cause of the intensification of symptoms at night may be due to the position of the wrist during sleep and/or fluid accumulation around the wrist while lying down.

This condition may be temporary and transient, spontaneously resolves, or it may be continuous and develop gradually. Patients may suffer with the development of the condition from a feeling of burning and/or cramping and weakness in the hand, and weakness of the hand grip leads to the repetition of falling objects from the hand. In the very advanced stages, with the chronicity of this syndrome, patients develop atrophy of the small muscles of the hand.

How is carpal tunnel syndrome diagnosed?
The diagnosis of carpal tunnel syndrome is based on the existing symptoms and a physical examination of the patient in addition to neurotransmitter studies. The physical examination includes examining the hand, wrist, shoulder and neck to look for any causes of nerve compression. The examination also includes swelling or abnormalities, as well as assessment of sensation in the fingers and hand muscle strength.

Symptoms can be induced by some tests where pressure is placed on the median nerve in the wrist area, or the wrist is bent downward, which increases pressure on the median nerve and symptoms appear. As for neurotransmitter studies, they are diagnostic tests that measure the speed of neurotransmission in the nerves, where it is noted that the transmission speed in the median nerve decreases as it crosses the wrist area.

How is carpal tunnel syndrome treated?
The treatment of carpal tunnel syndrome differs from one case to another. It depends on the severity of symptoms and the presence or absence of muscle weakness. Non-surgical treatment methods include avoiding the wrong positions of the wrist and using splints to fix the hand in an appropriate position, especially during sleep, in addition to drug treatment such as analgesics and non-steroidal anti-inflammatory drugs. Associated pathological conditions such as arthritis, and steroid injections into the carpal tunnel are also useful to reduce inflammation.

Surgical treatment may be necessary in the event of severe damage to the median nerve. Surgical work includes removing pressure from the nerve in the wrist by cutting the tissue that is compressing it, and the results are generally good.

How can carpal tunnel syndrome be prevented?
It can be prevented by modifying the lifestyle and avoiding positions that cause excessive pressure on the wrist, in addition to treating the accompanying conditions such as diabetes, high arterial pressure and arthritis.

the reviewer:

There is no doubt that sport helps a person build a strong body, and fight diseases and aging, but its practice is linked in some cases to the possibility of sports injuries, which are often caused by trauma or overuse of muscles or joints.
The chances of sports injuries increase if a person does not exercise regularly, or if this sport requires physical contact with others, or if he does not do warm-up exercises before exercising.

What are the types of sports injuries?
Different sports injuries produce different symptoms and complications. The most common types of sports injuries include:
• torn ligaments: ligaments are tissues that connect two bones together in a joint, and excessive tension may cause their rupture.
• A rupture of muscles or tendons, which are the cords of thick tissue that connect bone to muscle. Tennis elbow is one of the most famous examples, and is characterized by severe pain in the back of the elbow and forearm, and occurs due to overuse of the tendons in this area.
• Knee injuries, any injury that interferes with the normal movement of the knee joint can be a sports injury, and ranges from excessive stretching to a tear in the muscles or tissues of the knee.
• Swollen muscles. Swelling is a normal reaction to any injury. Swollen muscles are often painful and weak as well.
• Rupture of the Achilles tendon (Achilles tendon) is a thin and strong tendon located at the back of the ankle, and during exercise, this tendon may rupture or rupture. If this happens, the affected person will feel sudden, severe pain and have difficulty walking.
• Bone fractures. These fractures range from simple partial fracture (hair) to complex fractures. Most of these fractures occur in the arms and legs.
Dislocation of the joint. Sports injuries may lead to a dislocation of a joint in the body, as the bone is removed from its joint cavity. This is often painful and leads to swelling and weakness of the joint.
• Shoulder rupture. Four pieces of muscle work together to form a purse that protects the shoulder and moves it in all directions. A tear in any of these muscles can weaken them, and this can lead to a dislocation of the shoulder joint.
• Spinal stenosis: Spinal stenosis occurs when lifting heavy weights, which is especially true for weightlifting athletes.
How are sports injuries diagnosed?
Many sports injuries cause immediate pain and discomfort, while other sports injuries, such as muscle overuse injuries, may not be noticed until long-term tissue damage has occurred. These injuries are often diagnosed during clinical examinations or through routine examinations.
When someone has a sports injury, a doctor will likely take the following steps to reach a diagnosis:
• Taking a medical history, which includes asking questions about how the injury occurred, and the pattern and severity of the pain.
• Conducting a clinical examination. The doctor may try to move the affected part of the body or the affected joint, which helps him to determine the extent of joint movement and the extent of damage caused by the injury.
• Radiography. X-rays, magnetic resonance imaging (MRI), CT scans, and ultrasounds can help doctors and health care providers see body tissues and damage from an injury. , which contributes to the development of appropriate treatment.
How are sports injuries treated?
Often used to deal with athlete’s injuries, this five-point program includes protection, rest, ice, compression, and elevation.
• Protection. The injured tissue must be protected from any further injury, by applying bandages, elastic coverings, or simple splints.
• Rest. Injured tissues need time to heal, but the casualty can rest selectively. For example, he may have to give up tennis, but he can still walk or run.
• The use of cold compresses, which is the least expensive, simplest and most effective way to relieve pain, especially in the beginning. The cold causes the blood vessels to constrict and reduces blood flow to the affected area, reducing swelling and pain. For best results, apply an ice pack for 10 to 15 minutes as soon as possible after the injury, and repeat this every hour for the first four hours, then four times a day for two to three days.
• Light pressure on the affected part, the pressure will help reduce swelling and inflammation. In most cases, a simple elastic bandage is sufficient, but care must be taken not to be too tight, as applying excessive pressure may obstruct blood flow to the area and injure it.
• Elevating the affected limb. This is a simple strategy that uses the force of gravity to drain fluid away from the affected tissue, reducing swelling, inflammation and pain. Doctors recommend keeping the sore foot or affected limb elevated on one or two pillows in bed so that it remains higher than the rest of the body. Most often, this procedure helps relieve symptoms and speed up treatment as much as possible.

Despite this, some injuries may require medical or surgical intervention by specialized doctors, as is the case when dislocations and fractures occur, for example. Doctors prescribe pain relievers, the most important of which are NSAIDs, which reduce swelling and prevent inflammation. Splints are useful in case of fractures or to stabilize the affected joint, and surgery may be necessary in some cases. Most doctors resort to physical therapy in order to strengthen the muscles in the affected area to speed up recovery, and enable the patient to regain the ability to move as soon as possible and avoid relapse.

the reviewer:

 

The body’s natural immunity attacks foreign factors, so the body recognizes viruses, germs, pathogens and intruders and attacks them to limit their harm. In some cases, the body’s immunity is disturbed, and it recognizes its cells as a strange and pathogenic agent, so it attacks and harms them, and this is what happens in autoimmune diseases.

What is Behcet’s disease?
Behcet’s disease is a rare autoimmune disease in which the body attacks blood vessels, resulting in mouth ulcers, rashes, and other symptoms. The severity of symptoms varies from person to person.

Behcet’s disease is a chronic condition, the symptoms of which may disappear temporarily but recur at a later time. Symptoms can be controlled with medications and lifestyle changes in order to reduce the occurrence of serious complications such as blindness.

What are the symptoms of Behcet’s disease?
Symptoms of Behcet’s disease vary from person to person and may come and go or become less severe over time. Symptoms and signs depend on which parts of the body are affected. Areas commonly affected in Behcet’s disease include:
Mouth: Mouth ulcers appear as painful erosion of the oral mucosa. They are the most common symptom of Behcet’s disease. They begin as raised, round lesions in the mouth that quickly turn into painful ulcers. The ulcers heal within 1-3 weeks, but they may reappear.
• Skin: In some patients, acne-like sores appear on their bodies, and in others, raised, painful red nodules develop on the skin, especially the lower legs.
• Genitals: Red, open sores can appear on the scrotum (the scrotum) and the vulva, and they are usually painful and may leave scars.
• Eyes: Inflammation in the eye causes redness, pain and blurred vision, usually in both eyes, and this inflammation may appear for a while and then disappear. This inflammation may be dangerous if it extends to the retina, which threatens to blindness.
• Joints: Arthritis occurs in half of patients with Behçet’s disease, and causes pain, swelling and stiffness in the joints, especially the knee, ankle, elbow and wrist joints. Arthritis lasts for a few weeks and does not cause permanent joint damage.
• Blood vessels: Inflammation in the arteries and veins can cause redness, pain and swelling in the arms and legs when a clot forms. Inflammation in the large arteries can lead to complications such as an aneurysm or narrowing and blockage of the vessels.
• Gastrointestinal tract: Abdominal pain, diarrhea and gastrointestinal bleeding may occur.
• Brain: Inflammation in the brain and nervous system can cause headaches, fever, imbalance, seizures, or stroke.
What are the causes of Behcet’s disease?
Behcet’s disease is an autoimmune disease, meaning that the body’s immune system mistakenly attacks some of its healthy cells, and genetic and environmental factors likely play a role. There is a link between the occurrence of Behçet’s disease and some genes, and some studies suggest that a virus or a bacterium can induce this disease in people who carry certain genes.

Behcet’s disease symptoms and signs are thought to be caused by inflammation in the blood vessels, and this condition can involve arteries and veins of all sizes.

How is Behcet’s disease diagnosed?
No tests can confirm or deny that you have Behcet’s disease, so your doctor will rely mainly on your signs and symptoms. Diagnosis requires a combination of symptoms, and since mouth ulcers occur in nearly everyone with this condition, mouth ulcers that recur at least three times in 12 months are generally considered essential for a diagnosis of Behcet’s disease.

In addition, the diagnosis requires at least two other signs, such as the presence of recurrent genital ulcers, inflammation of the eye, skin ulcers, or others.

Your doctor will need to rule out other conditions that give similar symptoms, such as Crohn’s disease and reactive arthritis. Tests he might need include:
• Blood test: Although there is no laboratory analysis capable of proving the disease, laboratory tests are necessary to rule out the presence of other similar diseases.
• Multiple sensitivity test: In this test, your doctor inserts a sterile needle into your skin and examines the area after a day or two. If the test is positive, a small red bump forms where the needle was inserted, indicating that your immune system is overreacting to a small injury.
• Biopsy: A biopsy of an affected area can show vasculitis, which supports the diagnosis of Behcet’s disease.

How is Behcet’s disease treated?
Unfortunately, there is still no cure for Behcet’s Disease, and treatments are aimed at relieving pain and symptoms and minimizing complications.

Mild cases are treated with topical medications such as:
• Skin creams, gels and ointments: Topical corticosteroid medications are applied directly to skin ulcers and genital ulcers to reduce inflammation and pain.
Mouthwashes: Using a special mouthwash containing corticosteroids and other substances reduces the pain of mouth ulcers.
• Eye drops: Eye drops that contain corticosteroids and other anti-inflammatory can reduce pain and redness in the eyes if the inflammation is mild.
• Non-steroidal anti-inflammatory drugs such as ibuprofen are effective in relieving pain, but they have many side effects, the most important of which are peptic ulcers and kidney damage, so they should be taken after consulting a doctor.
• If topical medications do not help, your doctor may recommend a medication called colchicine to treat recurrent oral and genital ulcers and swollen joints. Colchicine is a treatment for gout, but it has been shown to be effective in treating Behcet’s disease.
Severe cases of Behcet’s disease require permanent medications to control the damage caused by the disease and reduce complications. These medications work to reduce the body’s immune reaction, so on the one hand they improve symptoms, but on the other hand the body becomes less able to resist infections. Among these medicines we mention:
• Corticosteroids: Corticosteroids such as prednisone reduce the inflammation caused by Behcet’s disease, and doctors often prescribe them with other medications to suppress the activity of your immune system. Long-term use of corticosteroids in high doses may lead to increased arterial pressure and osteoporosis.
• Medications that suppress your immune system: The inflammation associated with Behcet’s disease can be reduced by medications that prevent your immune system from attacking healthy tissue. These medications include azathioprine, cyclosporine, and cyclophosphamide.

What are the complications of Behcet’s disease?
Most symptoms of Behcet’s disease can be controlled and if properly treated, it is unlikely to cause permanent health problems. However, treating some symptoms is necessary to avoid long-term problems. For example, if an eye infection is not treated, the patient may become vulnerable to vision loss.

Behcet’s disease is a disease of the blood vessels, so serious vascular problems such as stroke, which occurs when something obstructs the blood flow to the brain, can occur. Inflammation of the arteries and veins can also cause blood clots to form.

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What is osteoporosis?
Osteoporosis causes bones to become so weak and easy to break that even a simple fall or exertion such as bending or coughing can fracture them. Within the healthy bone, there are small spaces resembling beehives, and in the case of osteoporosis, the size of these spaces increases, which results in the bones losing their strength and density, and in addition to this, the bone circumference is weaker and thinner. Osteoporosis can occur at any age, but it is more common in the elderly, especially women. The bones most commonly affected are the ribs, the hip, and the bones in the wrist and spine.

What are the symptoms of osteoporosis?
The early stages of osteoporosis cause no signs or symptoms. In most cases, people don’t know they have this condition until they have a fracture. Early symptoms if they appear include:
• Receding gums.
• Poor grip strength.
• Weak and brittle nails.

Osteoporosis can worsen without proper treatment, increasing the risk of fractures. Symptoms of severe osteoporosis include fractures that occur from a fall or even from severe sneezing or coughing. It can also include back or neck pain or lack of height as a result of a compression fracture, which is a break in one of the vertebrae in the neck or back that is so weak that it breaks under normal pressure on the spine.

If you have an osteoporotic fracture, the recovery time depends on several factors, including the location and severity of the fracture, your age and medical history.

What causes osteoporosis?
Osteoporosis is a disease of the elderly. Bones gradually lose their normal structure over time. In your 30s, your body begins to break down bone faster than it can replace it. This results in bones that are less dense, more fragile and therefore more susceptible to fracture.

Vulnerabilities of the year affect women more than men, and tend to affect people of Caucasian and Asian race more than others. Some factors can accelerate the occurrence of fragility, the most important of which are:
• Estrogen deficiency: menopause is associated with a faster loss of bone tissue in a woman’s body due to changes in hormone levels associated with its occurrence. Early menopause is also a risk indicator for osteoporosis.
• Hormonal disorders such as hyperthyroidism, and increased blood cortisol in Cushing’s syndrome.
• The use of some medications, such as corticosteroids, which are taken for a long time, orally or by injection, such as prednisone or cortisone.
• Factors that reduce the absorption of minerals such as severe malnutrition or malabsorption such as celiac disease, or wrong and prolonged diets.
• Lack of physical activity.
• Smoking.
• Decreased body weight.

How can osteoporosis be diagnosed?
Low bone density on a simple x-ray or CT scan can be the first warning sign of osteoporosis, and your doctor may notice signs of a fracture without symptoms.

When you suspect osteoporosis, your doctor will take your medical history and perform a physical examination. Your doctor may also order blood and urine samples to look for other causes that may cause bone loss, and he or she will ask you to take a bone density test (Dexa Scan).

This test uses low levels of X-rays to determine the mineral levels in the bones of the wrist, hip or spine, the most common areas affected by osteoporosis. This painless test takes about 10-30 minutes.
What are the possible treatments for osteoporosis?

If the test shows you have osteoporosis, your doctor will develop a treatment plan, prescribe medications and ask you to make lifestyle changes. These changes include increasing your intake of calcium and vitamin C, as well as getting proper exercise.

There is no cure for osteoporosis, but proper treatment can help protect and strengthen your bones, slow the breakdown of bone in your body, and some treatments can stimulate the growth of new bone.
The most common medications used to treat osteoporosis are bisphosphonates, which are used to prevent further bone mass loss. Bisphosphonates are taken orally or by injection.

Other medications that are used to prevent bone loss or stimulate bone growth include:
• Testosterone: Testosterone is the male hormone, and giving it to men can help increase bone density.
• Hormone therapy: For women, estrogen used during and after menopause can help stop the loss of bone density, but unfortunately estrogen therapy is also associated with an increased risk of blood clots, heart disease, and certain types of cancer, especially breast, colon and ovarian cancer.
• Raloxifene (Evista): This drug has been found to provide the benefits of estrogen without causing many risks, although there is still an increased risk of blood clots.
• Denosumab (Prolia): This drug is given by injection and can have even more promising results than bisphosphonates in reducing bone loss.
• Teriparatide (Forteo): an injectable parathyroid hormone that stimulates bone growth.
• romozuzumab (Efinity): This medicine is used to treat postmenopausal women who are at risk of fracture. This medication is given as two injections under the skin (in the same place) once a month for 12 months or less. This medicine can increase the risk of heart attack or stroke, so it is recommended to avoid it in people with heart problems.
There are promising studies on the role of stem cells in the treatment of osteoporosis in the future.

the reviewer:

What is congenital hip dislocation?
Congenital hip dislocation, or what is scientifically called developmental dysplasia of the hip (DDH), occurs when a child is born with an unstable hip, and this instability increases as the child grows.The hip joint resembles a ball (the femoral head) located within the pelvic cavity. In the case of dysplasia that occurs during the early stages of embryonic development, the socket becomes very shallow and does not fully contain the ball, resulting in instability and the joint may sometimes dislocate, meaning that the ball slips out of the socket with movement. Congenital hip dislocation is common, with an estimated 1 percent of every child affected by this disorder.

What are the causes of congenital hip dislocation?
The cause of congenital hip dislocation is unknown in many cases. Factors that contribute to this condition include decreased amniotic fluid in the womb, breech presentation i.e. the baby’s hips are born first instead of the head, and the presence of a family history of this condition. The fetus cannot move freely if the uterus is small, which hinders the normal development of the hips, so it is more likely that your baby will develop this condition if you are pregnant for the first time, because your uterus has not previously expanded.

Congenital hip dislocation is more common in females than males, but any baby can have it, so the doctor will check your baby after birth for signs of hip dislocation, and will continue to check your baby’s hip routinely during the first year of life.

Congenital hip dislocation is not usually associated with other problems or diseases, but the soft ligaments characteristic of some syndromes such as Ehler-Danlos and Marfan syndrome are unable to keep the femoral head within the socket, resulting in the appearance of hip dislocation. It can also be associated with some muscular and neurological problems such as cerebral palsy and meningocele.

Despite its name, a dislocated hip may not be present at birth, but rather develops during the first year of life. When the pelvic cavity is shallow, the hip is easily dislocated. Mistakes such as swaddling increase the risk of dislocation. Swaddling or wrapping the baby gives the newborn a feeling of comfort and warmth, which helps him sleep. However, tightening the baby’s legs to prevent movement may cause a dislocation of the hip joint in some cases.

What are the symptoms of congenital hip dislocation?
There are no symptoms of congenital hip dislocation in a newborn child. In older children, lameness may appear, movement of the legs outward, and a difference in the length of the legs, especially when only one hip is affected. When symptoms appear, the diagnosis is long overdue and treatment becomes difficult, so the child should be examined by an expert for signs of hip dislocation and not wait for the limp to appear.

How is congenital hip dislocation diagnosed?
Scanning for congenital hip dislocation is done at birth and during the first year of life, and the most common scanning method is a clinical examination. The child’s doctor moves the child’s hips and legs while listening for crackling or cracking sounds that could indicate a dislocation. The test is done in two stages and is called Barlow-Ortolani.
A routine examination of the hips includes looking for several signs, the most important of which are:
• Legs point outward or appear different in length.
• Specifies the range of motion.
• The folds on the legs and buttocks appear asymmetrical when the legs are extended.
Imaging tests can confirm the diagnosis Ultrasonography can be used for children younger than 6 months, and x-rays (X-rays) can be used to check older children, and many doctors recommend routine screening for hip dislocation even in the absence of symptoms, because late diagnosis is associated with Complex and painful surgeries and unsatisfactory results in many cases.

How is congenital hip dislocation treated?
If your child is younger than 6 months and diagnosed with a congenital hip dislocation, he or she will likely be treated with a soft brace called a Pavlik Harness. The child wears a saddle-like device that holds the legs in a frog-like position. The child may need to wear the saddle for 6-12 weeks depending on the age of the child and the severity of the condition, and may need to be worn permanently or intermittently depending on the severity of the condition.
If treatment with a Pavlik saddle is unsuccessful or the child is older than 6 months, the child may need more difficult procedures. The surgeon maneuvers to insert the hip into its socket. This is called closed dislocation. Or, surgeons may lengthen the tendons and remove other obstructions before putting the hip in place. This is called an open dislocation. After the hip is returned to its proper position, the hip and legs are placed in a splint for at least 12 weeks.
If the child is 18 months or older, or does not respond well to treatment, the doctor may have to cut part of the femur or pelvis to restructure the hip, meaning that the surgeon will reshape the femoral head or the acetabular socket.
What are the complications of congenital hip dislocation?

If hip dislocation is not detected in childhood or not treated properly, it may cause painful complications in adolescents and young adults such as degenerative arthritis or pain in the inguinal region during activities. The patient may also feel unsteady in the hip.

the reviewer:

What is clubfoot?
Clubfoot is a congenital deformity that causes a child’s foot to twist inward instead of outward, and the tissue that connects muscles to bones (tendons) is shorter than normal. This condition is usually recognized after birth, but doctors can also tell if a baby has club feet before birth by ultrasound. Although this condition usually affects one foot, it can also affect both feet. Clubfoot occurs in about one in every 1,000 live births, and it affects more often, for unknown reasons, males than females.

Clubfoot can sometimes be corrected by stretching it and placing a brace, but surgery may be necessary in severe cases.

What are the symptoms of clubfoot?
If this condition affects your child, the front of his foot is clearly pointing inward and outward, making his heel appear to be out of his foot while his toes point inward toward the other foot. In severe cases, the foot may appear to be upside down.

Children with club feet stagger while walking, often walking on the back of their affected foot to maintain balance.
Although club feet seem uncomfortable, they do not cause any pain or discomfort during childhood, although children may experience pain later in life. Children with clubfoot have a smaller calf muscle in the affected leg, and this leg may be slightly shorter than the unaffected leg.

What are the causes of clubfoot?
The exact cause of clubfoot isn’t known, but doctors agree that having a history (parents or siblings) increases the likelihood that a child will be born with the condition. Women who smoke or drink alcohol during pregnancy are also more likely to give birth to a baby with one or two feet with clubfoot, and the lack of amniotic fluid in the womb increases the risk. Clubfoot may also be part of a structural congenital malformation such as spina bifida, a birth defect that occurs when the spine and spinal cord do not develop or close properly.

How is clubfoot diagnosed?
The doctor can diagnose clubfoot by visually examining the foot of the newborn, and may sometimes order an X-ray image to see the severity of the clubfoot. Most cases of clubfoot can be noticed before delivery with a routine ultrasound in the 20th week of pregnancy. Do not assume that your child’s feet are clubfoot if they appear to be turned inward, as there are other abnormalities in the leg or bones in the foot that make the foot look abnormal.

How is clubfoot treated?
There are two effective ways to treat clubfoot: stretching and surgery. Surgery is used for severe cases, and stretching is used as an early treatment.

• Extension maneuver: Shortly after birth and before your baby starts walking, the doctor will show you how to maneuver and stretch your baby’s foot in a straight line. You should extend your baby’s foot daily to help it stay in the right position. This method is used in very mild cases.
• The Ponseti method: Another extension method that involves placing a splint on your child’s injured foot after extending it to a certain position. The doctor changes the cast every few weeks, or in some cases, every week or every few days. This process is repeated until the clubfoot is corrected, and the earlier it is started, the better the results.
The French method: Another extension method that involves applying duct tape to the club foot instead of using a splint. The doctor will likely continue this way until the child is 6 months old.
If scoliosis is corrected by extension, a splint or brace is placed on the leg every night for up to 3 years to keep the foot in the correct position.
• Surgery: If the clubfoot does not respond to manual maneuvering or if it is severe, surgery is necessary to correct it. The surgery is done to correct the position of the tendons, ligaments, bones and joints and bring them into proper alignment.

After surgery, the child must wear a splint for a year to keep the foot in the correct position.

What are the complications of club foot?
Clubfoot usually doesn’t cause any problems until your child starts standing and walking. If the clubfoot is treated, your child will likely walk fairly normally, but he may have some difficulties with movement as the affected foot is less flexible than the healthy foot and is slightly smaller, and the affected leg is slightly shorter in length but usually does not cause major problems .

But if it is not treated, clubfoot causes more serious problems, as a twisted ankle does not allow the child to walk on the soles of the foot, so the child tries to lean on the front or the outside of the foot, which leads to the appearance of ulcers on the foot that worsens the situation. Defective to weak growth in the calf muscles, and joint damage.

Parents should not neglect the psychological state of the child, as the abnormal gait may be embarrassing for the child, and poor balance may lead the child to try to avoid playing with his peers, which leads the child to isolation and depression.

the reviewer:

What is herniated vertebrae?
Your spine is made up of a series of bones (vertebrae) stacked together. The spine from beginning to end contains seven bones in the cervical spine, 12 in the thoracic spine, and five bones in the lumbar spine, followed by the sacrum and the coccyx at the bottom. These bones are separated by flexible discs. These discs absorb shocks that occur during daily activities such as walking, lifting objects and bending, and protect the vertebrae from rubbing against each other.

What is herniated vertebrae?
Each disc is made up of two parts: a soft gelatinous inner core and a hard, rubbery ring around the periphery. Injuries and weakness can cause a protrusion of the inner part through a tear in the peripheral ring. This is called a slipped, herniated, or herniated disc.
Spinal disc herniation can affect any part of your spine from the neck to the lower back, but most injuries occur in the lower back.

What are the symptoms of disc herniation?
Your spine is a complex network of vertebrae, nerves, and blood vessels. The spinal cord passes through a canal in the spine from which nerves branch. These nerves come out of the space between the vertebrae, so the absence of this space puts pressure on the nerves, causing the patient to feel pain and numbness along the affected nerve.
Symptoms of spinal disc herniation include:
• Lower back pain. This pain increases at night when coughing or making certain movements.
• Pain and numbness often on one side of the body.
• Pain spreading to the arms or legs.
• Pain that increases after standing or sitting.
• Pain when walking short distances.
• Unexplained muscle weakness.
• A feeling of tingling, pain or burning along the affected nerve.
• Inability to control urine or stool output.
Pain patterns vary from person to person. See your doctor when your pain results in numbness or tingling that interferes with your ability to control your muscles.

What are the causes of disc vertebrae?
Spinal disc herniations occur when the outer ring becomes weak or ruptures, allowing the inner part to slide out. This can happen with age, or due to certain movements and is more common in males than females. The disc can slip when you twist or bend to lift something. Lifting a very large, heavy object can cause great effort to be applied to the lower back, resulting in the disc slipping, and this is what happens during weightlifting.
The older you get, the greater your risk of herniated discs, because your discs begin to lose their protective gel content, and as a result can slip more easily.

Lifestyle plays a role in the occurrence of vertebral disc herniation, as it is believed that smoking reduces the supply of sufficient oxygen to the discs, so they are easily susceptible to disc herniation. Also, overweight people may also have a high risk of disc herniation because their discs have to bear more effort. On the other hand, the back muscles are weak in people whose work requires them
Sitting for long hours, or who are accustomed to a sedentary lifestyle, which increases the chances of them suffering from slipped discs.

How is disc herniation diagnosed?
The doctor first performs a physical examination trying to determine the source of the pain in your back, and asks you to lie on your back and move your legs in different directions to help him determine the cause of the pain. Your doctor may also perform a neurological exam to check your reflexes, muscle strength, your ability to walk, and the sensation of light touch, needle prick or vibrations.
A careful clinical examination may be sufficient to establish a diagnosis, but the doctor will often order auxiliary tests to confirm the diagnosis and rule out other infections that may cause similar symptoms, the most important of which are:
• X-rays: A simple image does not show herniated vertebrae, but it can rule out other causes of back pain such as infection, tumor, alignment problems, or a broken bone.
• Computerized tomography (CT Scan): It gives cross-sectional images of the spine and the structures surrounding it.
• Magnetic resonance imaging (MRI): Magnetic resonance imaging (MRI) is the best option to confirm the location of the disc and identify the affected nerves.
• Myelogram: It is an X-ray imaging after dye is injected into the spinal fluid. This test can show pressure on the spinal cord or nerves from herniated vertebrae or other conditions.
• Electromyography: Electromyography (EMG) and nerve conduction measures the quality of electrical impulses traveling along nerve tissue, helping to pinpoint the exact location of nerve damage.

How is spinal disc herniation treated?
Treatment for disc herniations ranges from conservative to surgical, depending on the severity of symptoms and the degree to which the disc has slipped from its location. Most people can relieve pain with an exercise program suggested by a physical therapist that stretches and strengthens the back and the muscles around it.

Pain relievers and avoiding heavy lifting can also help improve symptoms. Although NSAIDs are useful in relieving pain, they may cause stomach ulcers, so consult your doctor before starting to take them. Refraining from any movement activity because of the pain and discomfort caused by a herniated vertebrae may cause muscle weakness and joint stiffness, so the patient should try to stay active as much as possible by doing light activities such as walking.
If your herniated disc doesn’t respond to pain relievers, your doctor may prescribe stronger medications, such as:
• Muscle relaxants to relieve muscle spasms.
• Opiates to relieve pain.
• Neuropathic pain medications such as gabapentin or duloxetine.
• Local injections of steroids.

Your doctor may resort to surgery if symptoms do not subside within six weeks or if a herniated disc is affecting muscle function. The surgeon may remove the damaged or slipped part of the intervertebral disc without removing the entire disc. In more severe cases, the doctor may replace the disc with an artificial one, or remove the disc and fuse the two vertebrae together.

the reviewer:

What is scoliosis?
Scoliosis is an abnormal curvature of the spine that often occurs during a bulge of growth just before puberty, in which the spine appears curved from side to side or in an “S” or “C” shape.

What are the causes of scoliosis?
There is no clear cause for scoliosis in 80% of cases, but in some others the issue can be linked to problems in the nervous system or the motor system such as cerebral palsy and muscle weakness. The most common causes that doctors may be able to identify include the following:
• Cerebral palsy is a group of nervous system diseases that affect movement, learning, hearing, vision and thinking.
• Muscular dystrophy, a group of genetic diseases that cause muscle weakness.
• Congenital malformations that affect the bones of the child’s spine, such as spina bifida.
• Marfan syndrome.
• Vertebral collapse due to spinal injuries, infections, fractures, or severe osteoporosis.
Patients with a history of scoliosis are more likely to develop this condition, and females are more likely to have a severe form of scoliosis than males.

What are the symptoms of scoliosis?
About 3% of adolescents suffer from scoliosis, and most cases are mild and do not require treatment, but some of them become more severe as the child grows. Severe cases of scoliosis can be disabling and can reduce the space inside the chest, making it difficult for the lungs to function properly.

Symptoms vary according to the degree of scoliosis. Common symptoms associated with scoliosis include:
• One shoulder blade is higher or more prominent than the other.
• Hips are asymmetrical.
• Back pain.
• Breathing problems due to the lack of sufficient space inside the chest for the expansion of the lungs.
How is scoliosis diagnosed?
The first step your doctor takes to find out if you have scoliosis is a physical exam, and he or she may order some imaging tests to help diagnose.
The doctor will watch your back while standing with your arms at your sides, looking for curvature and symmetry in your waist and shoulders. Then the doctor will ask you to bend forward, looking for any curvature in the upper or lower back.
Imaging tests your doctor may order to diagnose scoliosis include:
• X-ray imaging: a simple image can confirm the diagnosis of scoliosis and reveal the severity of the curvature in the spine, and can also be used to monitor the progression of the disease.
• Magnetic resonance imaging (MRI): If the doctor suspects that there is an underlying condition causing scoliosis such as a tumor, he may order an MRI, which is useful for taking detailed pictures of the bones and surrounding tissues.
• Computerized tomography (CT Scan): A computerized tomography scan gives a three-dimensional image of the body.
• Bone Scan: This examination shows the locations of a radioactive substance that is injected into the body before the scan, as this substance is concentrated in places where blood perfusion increases, which determines the places of anomalies in the spine.

How is scoliosis treated?
Most children with scoliosis have a slight curvature and likely do not need treatment with braces or surgery. Instead, they can just have regular checkups to monitor changes in the curvature of their spine as they grow.

There are criteria for mild, moderate and severe cases, but the decision to start treatment varies according to each case. Factors to be taken into consideration include:
• Gender: Females have a higher risk of infection than males.
• Intensity of curvature: Large curvatures are likely to increase with time.
• Bending pattern: Double bending, also known as “S” bending, tends to be more severe than “C” bending.
• Location of the curvature: Curves that occur in the central (thoracic) segment of the spine tend to be more severe than those in the upper or lower sections of the spine.

Puberty: If a child’s bones stop growing, the risk of curvature is reduced, and this means that braces have the greatest effect in children whose bones are still developing.
Mild scoliosis does not need to be treated. In these cases, light exercises to strengthen the back muscles, such as relaxation exercises and yoga, are sufficient. Physical therapy may be helpful, and NSAIDs may be taken to relieve pain. These medicines may cause stomach ulcers, high arterial pressure, and kidney damage in some patients, so they should be used under the supervision of a doctor.

If your child’s bones are still growing and he has moderate scoliosis, the doctor may suggest that he wear a brace. Wearing a brace does not cure scoliosis, but it usually prevents its progression. Braces are stopped when the bones stop growing. Braces are often made of plastic and designed to match the body. This brace is nearly hidden under clothing and fits under the arms, around the rib cage, lower back, and pelvis. Braces do not impede movement. Children who wear braces are usually able to participate in most activities with some difficulty. If necessary, children can remove the brace to participate in sports or physical activities. Most braces are worn day and night, and the effectiveness of the brace increases with the number of hours a day is worn.

Severe scoliosis develops over time, so your doctor may suggest surgery to reduce the severity of the spinal curvature and to prevent it from getting worse. Spinal fusion surgery is the most common surgery used. Surgeons fuse two or more vertebrae in the spine together, so that the vertebrae cannot move independently. Pieces of bone or bone-like material are placed between the vertebrae. Rods, screws, and wire hold the curved portion of the spine straight and hold it until the old and new bone material has fused together.

If scoliosis progresses rapidly at a young age, surgeons can install a rod that adapts to the height increase that occurs as the child grows. The rod is fixed at the apex and end of the vertebral curvature and its length increases every 6 months. Complications of spinal surgery include bleeding, infection, pain and nerve damage.

the reviewer:

What is degenerative arthritis?
Degenerative Arthritis, also called Osteoarthritis. It is the most common chronic joint disease, affecting millions of people around the world.

First, the joint is where two bones meet, and the end of these two bones is covered with cartilage, a tissue that protects the bone from friction and facilitates movement. In degenerative arthritis, this cartilage is destroyed, causing the bones to rub together within the joint, resulting in pain, stiffness, and other symptoms.

What are the causes of degenerative arthritis?
Degenerative arthritis is considered a disease of the elderly, it occurs most often in the elderly, but it can affect adults of any age. The joint gradually begins to wear down and joint damage accumulates over time, which is why age is one of the main causes of degenerative arthritis. Other causes of joint injury include past injuries such as a meniscus tear, joint dislocation or ligament injuries, all of which are common in athletes. The presence of fractures close to the surface of the joint also causes damage to the cartilage and thus degenerative arthritis in the future.

Degenerative arthritis can affect any joint, especially the joints that bear body weight such as the knees and hips, especially in people who suffer from obesity, but it can affect other joints such as the joints of the hands, the spine, especially the neck and lower back.

What are the common symptoms of degenerative arthritis?
The most common symptoms of this disease are joint pain and joint stiffness, especially after rest periods or in the morning, and less movement. With the progression of the disease, the pain becomes more severe, and swelling may occur in the joint and the area around it, as well as deformation in the shape of the joint.

How is degenerative arthritis diagnosed?
Degenerative arthritis is a slow-developing disease that is difficult to diagnose in its early stages. As the disease progresses, joint pain occurs that increases in intensity and frequency with the progression of the disease. During the clinical examination, the doctor examines the affected joint for the presence of tenderness, swelling or redness, and the doctor often needs to request laboratory and radiological investigations to confirm the diagnosis and rule out other similar diseases.

What are the auxiliary examinations?
Laboratory tests do not provide a direct benefit in diagnosing degenerative arthritis, but they are important to rule out other conditions that cause joint pain, such as rheumatoid arthritis. It is also possible to perform a joint fluid analysis to determine whether gout or septic arthritis is the cause of the infection.

X-ray imaging: the cartilage often does not appear on the simple picture, but the joint loss appears in the form of narrowing of the space between the two bones in the joint, and the simple picture shows bony bumps around the joint, and abnormal growth of the bone, and small fluid-filled cysts may appear within articular cavity; An expert radiograph is important for diagnosing degenerative arthritis, and may be sufficient alone to make the diagnosis.
Magnetic resonance imaging (MRI): An MRI that produces detailed images of bone and elastic tissue, including cartilage, is not usually used to diagnose degenerative arthritis but provides important information in complex cases.

How is degenerative arthritis treated?
Treatment for degenerative arthritis is based on symptomatic management. Treatments can reduce pain and help the patient move better.
Medicines that can help improve symptoms of degenerative arthritis and relieve pain mainly include:
• Acetaminophen: Acetaminophen has been shown to be effective in patients with mild to moderate pain.
• Nonsteroidal anti-inflammatory drugs (NSAIDs): Over-the-counter NSAIDs, such as ibuprofen and naproxen sodium, usually relieve pain. Stronger NSAIDs can be obtained by prescription. In some cases, NSAIDs cause stomach ulcers, heart and blood vessel problems, bleeding and damage to the liver and kidneys, so they should not be taken without medical advice.
Topical NSAIDs are effective in relieving symptoms, and are safe and have fewer side effects. NSAIDs are applied in gel form to the skin over the affected organ.
• Duloxetine: Usually used as an antidepressant, this drug is approved for the treatment of chronic pain, including degenerative arthritis pain.
Other treatment methods include:

• Physiotherapy: The physiotherapist can teach the patient how to do exercises to strengthen the muscles surrounding the joint and increase their flexibility. Alternating cold and warm compresses is effective in relieving joint stiffness. It may also be used for regular and light exercises that you do yourself, such as swimming and walking. Same efficacy.
• Occupational therapy: An occupational therapist can help you explore ways to perform daily tasks without putting extra stress on your aching joints, such as using a long-handled toothbrush and having a shower seat.
If conservative treatments don’t help, your doctor may suggest other treatments, such as:
• Cortisone injections: Injecting corticosteroid medications may relieve joint pain. The doctor numbs the area around the joint, then injects the medication into the empty area of ​​your joint. The number of cortisone injections you can take each year is generally limited to three or four, because the medication may worsen joint damage over time.
• Lubricant injection: Some research indicates the benefit of injecting hyaluronic acid into the knee, as hyaluronic acid is similar to a compound usually found in joint fluid, and its injection may help facilitate the movement of the affected joint.
• Surgical treatment: If degenerative arthritis damages one side of your knee more than the other, osteotomy may be beneficial where the surgeon cuts the bone either above or below the knee, then removes or adds a bony wedge. This process helps shift your body weight away from the damaged part of your knee.
• Joint replacement: In a joint replacement (arthroplasty), the surgeon may remove damaged surface parts of your joint and replace them with plastic or metal parts.

the reviewer:

What is osteomyelitis?
Osteomyelitis is an infection of the bone caused by bacteria or fungi that invade the bone. In children, it occurs mostly in the long bones of the arms and legs, but in adults it usually appears in the hip bone, spine and feet. Osteitis can occur suddenly or develop over a long period of time. If not treated properly, osteomyelitis can leave permanent bone damage.

What are the causes of osteomyelitis?
Many pathogens, the most common of which are Staphylococcus aureus, travel in the bloodstream and may cause osteitis. Sepsis can start in any area of ​​the body and spread to the bones through the bloodstream. And pathogens that invade a severe injury such as a deep wound can cause inflammation in nearby bones. Bacteria can also enter through the site of a previous surgery, such as where a hip replacement or a broken bone was repaired. When a bone breaks, bacteria invade the bone, causing osteomyelitis.

What are the risk factors?
There are some conditions and conditions that increase the risk of developing osteomyelitis, including:
• Recent injuries or orthopedic surgery: Where fractures or deep wounds allow bacteria to enter the bones and tissues close to them, joint replacement surgery performed in the event of joint wear, such as in degenerative arthritis and rheumatoid arthritis, can make way for bacteria to enter the bones.
• Disorder of blood perfusion to the bones as in:
• diabetic.
• Sickle cell anemia.
• Peripheral arterial disease, which is often caused by smoking.
• Conditions that require an intravenous line or catheter, such as:
• The use of medicines taken intravenously.
• Hemodialysis, which is used in cases of chronic renal failure.
What are the symptoms of osteomyelitis?
Usually the first sign that appears is pain at the site of the inflammation. Other common symptoms include:
• Fever and chills.
• Swelling in the inflamed area, and the skin is red and warm.
• Irritability or general discomfort.
• Drainage (oozing of pus) from the affected area.
• Inability to use the affected limb.

How is osteomyelitis diagnosed?
Your doctor can use several methods to diagnose the condition if you find any symptoms of osteitis, in order to differentiate them from other conditions that may show similar signs and symptoms, such as osteosarcoma, gout and septic arthritis. The doctor usually begins with a physical examination to check for swelling, pain, or discoloration, and will likely order blood tests to look for microorganisms that cause infection. Other tests done to look for bacteria are throat swabs, urine culture, and stool analysis (such as stool culture).
Imaging tests such as:
• X-ray imaging: It can reveal damage to the bone, however, the damage may not be evident on the simple image until several weeks have passed since the onset of the infection.
• Magnetic resonance imaging (MRI): Magnetic resonance imaging can provide detailed images of the bone and the soft tissues around it. It is not only useful in diagnosing osteomyelitis but also can help estimate the time that has passed since its onset.
• Bone Scan: It uses radioactive materials that show cellular and metabolic activity in the bone tissue.
In some cases, it is necessary to take a sample of bone for analysis, which is called a bone biopsy, which may show the type of germs that caused the infection. The surgeon inserts a long needle into the bone through the skin to take a biopsy. This procedure may require local anesthesia for the area where the needle will be inserted. X-rays or other imaging methods may be used to guide the needle.

How is osteomyelitis treated?
There are several options that a doctor may use to treat osteomyelitis. In some cases, drug therapy is sufficient, and antibiotics are given intravenously initially, and antibiotic treatment is long, up to six weeks.
In some cases, osteomyelitis may require surgery, in which the surgeon removes the affected bone and dead tissue and drains any abscesses (collections of pus). Artificial organs (such as an artificial joint), if present, must be removed and replaced with a new one.

What are the complications of osteomyelitis?
The condition of the bone deteriorates in the absence of treatment, and the inflammation increases in severity, and spreads to other areas. Untreated osteomyelitis can cause a number of complications, the most important of which are:
• Osteonecrosis: Osteomyelitis may obstruct the blood supply to the bone, causing necrosis, and this requires removing the necrotic areas so that the antibiotics can play their role effectively.
• Septic Arthritis: It may occur due to the spread of inflammation to a joint adjacent to the affected bone.
Bone growth disorder: The normal growth of bones or joints in children may be affected if osteomyelitis affects the soft areas called growth plates at the end of the long bones in the arms or legs.

the reviewer:

What is flat feet?
The structure of the foot is very complex. The human foot is made up of 26 bones, 33 joints, and more than 100 muscles, tendons, and arches. These arches give the foot a flexible structure that enables it to walk, run and move, while at the same time giving it sufficient stability so that it can support the weight of the body.

You are considered flatfoot when the arch (bending) of the sole of your foot is flat, causing the entire sole of your foot to touch the ground when you stand on your feet. Flat feet can occur when the curvature does not develop during childhood, and is a common and painless condition. In some cases, flat feet develop after a foot injury, or occur over time as a result of stress and fatigue accumulated over time.
Flat feet may sometimes be associated with problems in the ankles and knees, because this condition may cause a change in the alignment of the leg.

What are the symptoms of flat feet?
Most people do not have signs and symptoms associated with flat feet. But some people may experience pain, especially in the heel or arch of the foot, or feel sore or numbness in the foot. The pain can increase with activity and movement, and swelling can occur along the bottom of the ankle.

What are the causes of flatfoot?
Flat feet are considered normal in children and infants because the arch of the foot has not yet developed. Most arches develop during childhood, but some people never develop these arches. This change is normal in the shape of the foot, some people who do not have this arch suffer from problems, and others go about their lives normally without any complaints.

Some children have flexible flat feet, where the arch of the foot appears when the child is sitting or standing on tiptoe but disappears when he stands on his feet, most children get rid of flexible flat feet without problems.
The arch of the foot can wear off over time, as years of effort and wear can weaken the tendons that run along the bottom of the ankle and help support the arch.

What are the factors that increase the likelihood of flat feet?
Risk factors that increase the risk of developing flatfoot include:
• Obesity.
• Injury to the foot or ankle area.
• Rheumatoid arthritis.
• the age.
• diabetic.
How is flatfoot diagnosed?
The doctor will watch your feet from the front and back to monitor the way your feet move, and ask you to stand on tiptoe. The wear pattern on your shoes may be seen. In some cases, the doctor needs to order assistive radiological examinations, especially when the pain is severe, or when he suspects inflammation in the joints or tendons.
What are the types of assistive imaging tests?
If you have severe pain in your feet, your doctor may order tests such as:
• X-ray imaging: A simple image is useful in showing arthritis in particular.
• Computerized tomography (CT Scan): A computerized tomography scan provides more accurate information than a simple image.
• Ultrasound: The doctor may order this test if he suspects damage to the tendons. Ultrasound imaging gives accurate pictures of the soft tissues in the body.
• Magnetic resonance imaging (MRI): Magnetic resonance imaging provides fine details of both hard and elastic tissues.

How is flat feet treated?
Remember that flatfoot is healthy, doesn’t get in the way of any work, and isn’t usually associated with any serious illness. Thus, there is no need to treat flat feet if they are not causing pain. If flat feet are painful, the doctor may suggest one of the following methods:
Arch supports (orthotics): Over-the-counter arch supports may relieve pain from flat feet. Your doctor may suggest custom-made arch supports that are molded to the shape of your foot. Arch supports don’t cure flat feet, but they often relieve symptoms.
Stretching exercises: Some people with flat feet have a short Achilles tendon, and exercises may help to stretch this tendon.
• Supportive shoes: A structurally supportive shoe may be more comfortable than sandals or shoes with a low level of support.
• Physical therapy: Flat feet may cause repetitive injuries in some runners. Your physical therapist may show you a demonstration video to help you improve how you run.
Lifestyle changes: Reducing the pain of flat feet may require some changes to your daily routine. For example, your doctor may recommend that you follow a diet and exercise program to lose weight and thus reduce pressure on your feet, and may also recommend not standing or walking for long periods.
• Medications: Medications are not routinely prescribed, but they may be a good option to relieve pain or inflammation, if present. Nonsteroidal anti-inflammatory drugs (NSAIDs) can relieve pain and swelling, but they increase the risk of peptic ulcers, so they should be used with caution and under medical supervision.
• Surgery: Not only is surgery done to correct flat feet, but surgery may be done for an accompanying problem such as a tendon rupture or fracture. An orthopedic surgeon may create an arch in your foot, repair tendons, or fuse bones and joints. If the Achilles tendon is short, the surgeon may lengthen it to relieve pain.

the reviewer:

What is gout?
Gout is a common and complex type of arthritis that can affect anyone. It is characterized by sudden, severe attacks of pain, swelling, redness and tenderness (tenderness to touch and move) in the joints, most often the joint at the base of the big toe.

A gout attack can occur suddenly and often awakens the patient in the middle of the night. Some patients describe feeling like their big toe is on fire. The affected joint is hot, swollen, and painful to the touch. Even the weight of a sheet of paper on it causes excruciating, unbearable pain.

What are the symptoms of gout?
Symptoms and signs of gout often occur suddenly and at night, and include:
• Severe joint pain: Gout usually affects the large joint of the big toe, but it can affect any joint. Other joints commonly affected include the ankles, knees, elbows, wrists and fingers. The pain tends to be most intense during the first 4-12 hours after its onset.
• Persistent discomfort: After the severe pain has subsided, some joint discomfort may persist from a few days to several weeks, and subsequent attacks are likely to last longer and affect more joints.
• Limits the range of motion: With the development of gout, the patient may become unable to move his joints normally.

What are the causes of gout?
Gout occurs as a result of the accumulation of urate crystals in the joints, causing severe inflammation and pain. These crystals form when there are high levels of uric acid in the blood.

The body produces uric acid when it breaks down purine, a substance naturally found in small amounts in the blood. Purine is also found in some foods such as steak, organ meats, and seafood. Certain other foods increase uric acid levels, such as alcoholic beverages, especially beer, and drinks sweetened with fruit sugar (fructose).

In the normal case, uric acid is dissolved in the blood and excreted through the kidneys with urine, but sometimes an imbalance occurs between the production of this acid and its excretion, when a person eats a lot of purines or when his kidneys are not able to excrete wastes in a normal way due to a defect in them. Excess uric acid builds up, forming sharp, needle-like crystals in joints or nearby tissues, causing pain, inflammation, and swelling.
Some diseases can play a predisposing role for gout, such as diabetes mellitus, high arterial pressure, and heart and kidney diseases.

How is gout diagnosed?
Tests that help diagnose gout include:
• Joint fluid examination: The doctor may use a needle to withdraw fluid from the affected joint, as it is possible to see urate crystals when the fluid is examined under a magnifier.
• Blood tests: Your doctor may recommend a blood test to measure uric acid and creatinine levels. Although it is sometimes misleading, some people have high levels of uric acid and never had gout, and some people have signs and symptoms of gout but the levels of uric acid in their blood are normal.
• X-Ray: An X-ray of the joint may help rule out other causes of arthritis such as rheumatoid arthritis, inflammatory arthritis, degenerative arthritis, and psoriatic arthritis.
• Ultrasound imaging: Ultrasound imaging of the musculoskeletal system may show urate crystals in the joints.
Dual energy CT scan: This type of imaging can identify the presence of urate crystals in joints, even when they are not acutely inflamed, but is not routinely used in clinical practice due to its high cost and unavailability Wide.
How is gout treated?
The treatment plan for gout depends on the stage and severity of the disease. Medicines used to treat gout work in two ways: they either relieve inflammation and pain, or they prevent future attacks of gout by lowering uric acid levels.
Medicines that relieve gout pain include:
• Non-steroidal anti-inflammatory drugs (NSAIDs): such as aspirin, ibuprofen and naproxen, and they are considered effective in relieving pain, but they increase the risk of stomach ulcers, so they must be used under medical supervision.
• Colchicine.
• Corticosteroids are used in the form of pills or as an injection into the joint. Doctors usually try to avoid giving cortisone because of its many side effects.
Medicines that prevent gout attacks include:
• Inhibitors of xanthine oxidase such as allopurinol and febuxostat.
• Probenecid.
In addition to medications, your doctor may suggest lifestyle changes to help you control symptoms and reduce the risk of future gout attacks. For example, your doctor may encourage you to:
• Drink water in sufficient quantities.
• Minimize drinking alcohol.
• Weight Loss.
• stop smoking.
• Reducing the consumption of red and organic meat and seafood due to their high purine content.

What are the complications of gout?
People with gout may develop more severe conditions, such as:
• Recurrent gout: some gout patients may not suffer from its symptoms again, while gout attacks may occur in other patients every year. Taking gout medications may help prevent recurring attacks. If left untreated, gout can cause joint wear and tear.

Chronic gout: If gout is not treated, it may eventually cause the accumulation of hard lumps of urate crystals called tophi in the joints, skin, and surrounding soft tissues. Tophi can occur in several places such as the fingers, hands, feet, elbows, or in the Achilles tendon along the back of the ankles. Tophi are usually not painful, but they may become swollen and painful during gout attacks. These clusters cause permanent damage to the joints, and in rare cases, tumors may compress the median nerve in the wrist, causing carpal tunnel syndrome, so appropriate treatment is necessary to prevent gout from turning into a chronic disease.
• Kidney stones: Urate crystals can accumulate in the kidneys, causing kidney stones.

the reviewer:

What is craniosynostosis?
It consists of a group of bones, separated by fissures called sutures. These sutures are open at birth and remain so until age when they will close into solid bone. These cracks or seams open on the outside allow it to grow and develop. In some cases, these sutures close early due to a defect before the baby’s brain is fully formed, collectively becoming hard and stiff, hampering brain development. This condition is called craniosynostosis.
It happened intact, intracranial pressure rises.

What are the types of craniosynostosis?
There are several types to give in the picture, and that’s at about 80-90%, in this case the skull can work with the upper side at the expense of the other and the drawing appears asymmetrically.

In some cases, all sutures close early, making them small, and brain development is affected. Classify these complex cases with genetic syndromes.

What are the symptoms of craniosynostosis?
The condition and symptoms that were found in the child’s situation were based on the phenomenon in which the ossification occurred, the more the ossification was, the more cases and symptoms it was found, and the symptoms were more severe and the condition worse.

The symptoms of drowsiness are clearly visible at birth or several months later, from:
• Asymmetrical graphic shape.
• Absence of the fontanelle (which is the soft area in the baby’s head.)
• The presence of a hard and raised edge along the suture that closed too early.
• Abnormal growth of the child’s head.
And the rise in pressure appeared within physical symptoms, which appear intermittently, such as:
• Headaches in older children.
Vomiting, vomiting, spitting, or like a fountain.
• The eye socket is wide, narrow, or asymmetric in the shape of the eyes.
• The eyes are facing downward, and the child cannot forward, and it resembles the view of the sunset.
• Changes in the child’s awareness, some children tend to sleep excessively, and it is difficult to wake him, while some are irritable

What are the causes of craniosynostosis?
The cause of craniosynostosis is often unknown, but craniosynostosis is sometimes associated with genetic diseases such as Apert syndrome, Pfeiffer syndrome and Crouzon syndrome, which may affect the development of a child’s skull. These syndromes also include other physical abnormalities such as malformations of the limbs, abnormalities of the ears, and congenital heart lesions.

How is craniosynostosis diagnosed?
Craniosynostosis should be evaluated by a specialist in pediatric neurosurgery or a specialist in plastic and reconstructive surgery. The diagnostic tools used include:
• Clinical examination: The doctor examines the child’s head for any abnormalities such as raised edges and facial deformities.
• Imaging tests: Computerized tomography (CT Scan) or magnetic resonance imaging (MRI) of the child’s skull can show any fusion of the sutures. The fused sutures are recognized by their absence, disappearing once fused, or by the edge that appears along the suture line. Laser scans and photographs can also be used to take precise measurements of the shape of the skull.
• Genetic testing: If a doctor suspects a child has a genetic syndrome, genetic testing will help identify it.
What is the treatment for craniosynostosis?
The aim of the surgery is to secure space for the brain to grow and develop. In a few cases, brain development is acceptable, but the shape of the skull is distorted, then wearing a helmet designed to correct the shape of the skull during brain development can be sufficient without resorting to surgery.
Most children with this condition require surgery to correct the shape of the head and relieve pressure on the brain. The type of surgery depends on the affected suture and the condition that caused the ossification. Surgeons can repair affected sutures with the following operations:
• Laparoscopic surgery: The results of laparoscopic surgery are good in children younger than 3 months, and it can be used in children from 6 months of age if there is only one suture affected. During the operation, the surgeon makes one or two cuts in the child’s head, then inserts a light tube with a camera at the end to help him remove the bone above the fused suture.
Laparoscopic surgery is a good option as it causes less satisfaction and therefore recovery time is shorter and blood loss is less. The child may need to wear a special helmet for 12 months after that to correct the shape of the skull.
• Open surgery: Open surgery can be performed on children up to 11 months of age. In this process, the surgeon makes a large incision in the child’s head, then lifts the bones in the affected area of ​​the skull, reshapes them, and then puts them back in place. Reconstructed bones are fixed by plates and screws that eventually loosen automatically. Some children need more than one surgery to correct the shape of the head. Children undergoing this procedure do not need to wear a helmet afterwards. On the other hand, open surgery involves greater blood loss and a longer recovery period than laparoscopic surgery.

How is craniosynostosis monitored?
In the short term, this surgery is considered a complex operation, and it can cause many complications, so a doctor should be consulted immediately if the parents notice a rise in temperature, vomiting, or a change in the child’s awareness. The child also needs long-term follow-up and frequent examinations to assess the presence of problems in the bones of the face and jaws and treat them as early as possible.

The family also needs genetic counseling to investigate the presence of genetic syndromes, especially when there are other accompanying abnormalities.
If the condition is not treated, the child’s head may become permanently deformed. As the child’s brain grows,

pressure inside the skull increases, causing many problems, including:
• blindness.
• Poor mental development.
• Delayed growth.
• Eye movement disorders.
• Epileptic seizures.
• Problems with development and learning, difficulty in dealing with peers, and psychological problems.
• Death, in rare cases.

the reviewer:

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It is a type of bone cancer that begins in the cells that make up the bones, and it often affects the long bones, especially the bones of the legs and sometimes the arms, but it can occur in any bone, but in very rare cases, sarcoma can affect the elastic tissues outside the bone. Osteosarcoma tends to occur in adolescents and young adults, but it can occur in younger children and adults. Treatment often includes chemotherapy, surgery, and sometimes radiotherapy. Doctors choose treatment based on where the sarcoma begins, its type and stage, the size of the tumor, and whether the cancer has spread beyond the bones.

Why does osteosarcoma occur?
It’s not clear what causes osteosarcoma, but this cancer is known to form when one of the cells responsible for making new bone goes wrong. The genetic material of the cell contains instructions that control the growth and reproduction of the cell. Cells multiply to compensate for damage or breakage in the bone, for example. When these instructions are disturbed, the cells begin to make new bone when there is no need for it, and the result is a mass (tumor) composed of poorly formed cells that can form They invade and destroy healthy tissue in the body, and these cells can separate and move to distant sites (metastases).

People who have a family member who has had the disease, retinoblastoma or neurofibromatosis, or who have been treated with radiation are more likely to develop osteosarcoma.

What are the symptoms of osteosarcoma?
Osteosarcoma signs and symptoms include:
• Swelling near the bone.
• Bony pain that increases at night and does not respond to analgesics.
• Bone damage or fracture for no apparent reason.
• redness.
• He stopped.
• Determines the movement of the joints if the tumor is close to the joint.
How is osteosarcoma diagnosed?
A doctor can use different tools to diagnose osteosarcoma. He first starts by doing a clinical examination, where he looks for swelling and redness, and he may also request information about previous diseases and medical treatments, and he may ask to take a blood sample from the patient to look for tumor markers, which are chemical readings in the blood that indicate the presence of cancer. Other tests used to diagnose osteosarcoma include:
X-ray imaging: gives images of dense structures inside the body, including bones, and distortion in the shape of the bone may indicate the presence of a tumor.
Computerized tomography (CT scan): It is a three-dimensional imaging used to examine the bones and flexible organs in the body, and is considered important to know the spread of the tumor, especially to the lungs.
Magnetic resonance imaging (MRI): Magnetic resonance imaging gives clear pictures of the internal structures in the body, and is characterized by its ability to clearly see the tissues surrounding the bone, so it can show the size of the tumor and its spread to neighboring organs.
Positron emission tomography (PET Scan): It is a comprehensive examination of the body that is usually used to determine the presence of cancer, where a special radioactive substance is given, which the body eliminates within a short period. This material is absorbed by the active cancer cells and appears in a clear dark color on the x-ray.
Taking a sample of cells for examination (biopsy): A biopsy procedure is used to collect a sample of suspicious cells for laboratory testing. Tests performed on a biopsy can show if the cells are cancerous or not, and laboratory tests can determine the type and aggressiveness of the cancer cells, and help determine the best treatment plan for the patient.

Types of biopsy procedures used to diagnose osteosarcoma include:
Needle biopsy: The doctor inserts a thin needle through the skin and guides it into the tumor. The needle is used to take small pieces of tumor tissue.
Surgical biopsy: The doctor makes an incision in the skin and removes either all or part of the tumor.
Determining the type of biopsy to be performed and the details of how it should be performed require careful planning by the medical team so that they do not affect future surgery to remove the tumor.

What are the ways to treat osteosarcoma?
Osteosarcoma treatment involves a team of surgeons, chemotherapy and radio-oncologists.
• Chemotherapy: Doctors recommend chemotherapy before surgery as a “pre-treatment”, and monitor the response of cancer cells to it before making the next treatment plan. This method of treatment uses drugs that help shrink and kill cancer cells in order to reduce the size of the tumor. The type and duration of chemotherapy is determined by the type of cells and the extent of their spread outside the bones.
• Surgery: The goal of surgery is to remove all of the cancerous cells, but planning for the operation also takes into account how it will affect your ability to continue with your daily life. Surgeons try to avoid and preserve the limb by removing the tumor and surrounding bone tissue, and replacing the missing bone with an artificial one. Chemotherapy may be continued after surgery to destroy any microscopic cancer cells.
Radiation therapy: Osteosarcoma does not usually respond well to radiotherapy, so this therapy is used when the tumor has spread widely.

Some centers also rely on other treatment methods such as cryotherapy and immunotherapy, and many researches give hope that stem cell therapy can be used successfully.

Osteosarcoma is considered a recurrent disease after the completion of treatment, and most cases of recurrence occur in the first five years, so the patient must commit to visiting the doctor and performing the necessary clinical examination and laboratory tests, and investigating the emergence of new tumors by computerized tomography (CT scan) and x-ray imaging (X-Ray) and magnetic resonance imaging (MRI).

the reviewer:

Painful inflammation of the elbow joint caused by tendon stress, often caused by repetition of moving the wrist and going. For example, according to its name, tennis elbow does not only affect athletes, but also includes people who use this type of movement in their jobs, including plumbers, painters and carpenters. It is centered on the elbow in tennis elbow, but it may spread to the left to the left.

What are the causes of the cause of the occurrence of tennis?
The tendon is the part of the muscle that attaches to the bone. The tendons of the forearm attach the muscles of the forearm to the outside of the bone in the elbow. The stress leads to the muscles, where the repetitive use leads to the elbow. When lacerations occur repeatedly, the injury accumulates and the patient feels more pain.
Resulting from an activity This activity includes the following:
• Practicing tennis or other racket sports.
• Exercising the body.
• Use a screwdriver, hammer, or computer mouse frequently.
What are the symptoms of tennis elbow?
Tennis elbow patients may experience the following symptoms:
• Elbow pain that is mild at first and then becomes gradually.
• Feeling lying from the outside of the elbow down to the forearm and wrist.
• Difficulty using strong objects.
• Pain that increases when shaking hands or squeezing something.
• Pain when lifting something, using tools, or opening jars.
How is tennis elbow diagnosed?
It is generally diagnosed during a clinical examination. Diagnosis started. Apply some pressure on the point where the tendon attaches to the bone to detect the pointer.
A pity that the picture of tennis elbow.
X-ray imaging tools.
• X-rays (X-rays): X-rays give clear rays on the rays that appear in the rays that appear in the rays, as well as the X-rays.
Magnetic (MRI): Magnetic. Your picture appears in pictures from pictures shown in the following picture: pictures of soft tissues, they will help find out if you have possible discoid vertebrae or joints in your neck, and distinct varieties of stars in the arm.
Electrical illustrations (EMG) can be requested.

What are the ways to treat tennis elbow?
Approximately 80-90% of cases of his disease can be successfully treated without modification to the page. Your physician will initially suggest one or more of the following treatments:
• Rest: This is the first step to your recovery. You may need to have a comfortable splint near the affected limb, and it may be helpful.
• Cold compresses: can help relieve pain.
• NSAIDs: http://www.factory.com
• Physical therapy: The physical therapist uses, to strengthen the muscles of the forearm and speed up recovery. These exercises include forearm exercises, ice massage, and muscle stimulating techniques.
• Ultrasound therapy: The ultrasound probe is placed on the most common area of ​​the arm, and this probe sends high-frequency sound waves into the tissues for a certain period of time. This type of treatment can help reduce inflammation and speed healing.
The drug causes the drug immediately in the common condition in which the drug is used, such as arterial hypertension and osteoporosis. Symptoms improve quickly after taking the medication.
• Shockwave Therapy: An experimental treatment that delivers sound waves to the elbow to improve shock wave therapy by the study you are using itself.
• Plasma injection with platelets: a relatively new treatment option with promising results.
The upper part of the upper part can be used from the outer part, the upper part is used from the upper part, and the upper part is used from the inner part of the dead tissue. This operation was performed on your hand, as this operation was performed successfully.
The revision surgery was performed at some point between 80-90%.

the reviewer:

Our bones were found to be strong and sturdy to be able to carry the weight of the body, so any disease that affects these bones and loses their strength and hardness will affect their function. Rickets is one of the most important of these diseases, especially as it affects young people and affects their growth and development.

What is rickets?
Rickets is a disease of the skeleton caused by a deficiency of vitamin D or certain minerals such as calcium or phosphate. These nutrients are essential for building healthy and strong bones. People with rickets have soft bones and poor growth, and in severe cases severe osteomalacia leads to skeletal deformities.

What are the causes of rickets?
Rickets is more common in children between the ages of 6-36 months. During this period of time children grow rapidly, and their bodies need calcium and phosphate to strengthen and grow their bones properly. Your child needs vitamin D to absorb calcium and phosphorous naturally from food, and a child can develop rickets if he does not get enough vitamin D.

There are two main sources of vitamin D, sunlight and food.
Sunlight: Your baby’s skin produces vitamin D when exposed to sunlight. Some factors may affect the skin’s ability to synthesize vitamin D. The skin of dark-skinned children is less able to synthesize it. Also, children who live in areas that are not sunny are not exposed to enough sunlight. Sick children are forced to stay indoors for long periods of time due to their health condition, which will later expose them to rickets.

Children nowadays tend to spend most of the time indoors, and they are likely to use sunscreen, which blocks the arrival of the rays that stimulate the skin’s production of vitamin D, and severe air pollution hinders the arrival of the rays in sufficient quantities to the skin.

Food: Fish oils, egg yolks, and fatty fish such as salmon contain vitamin D. Many countries add vitamin D to some foods and drinks such as milk, cereal, and some fruit juices. Some children avoid dairy products due to their sensitivity to milk sugar (lactose deficiency), which exposes them to rickets, and children who are fed only breast milk can also develop vitamin D deficiency because breast milk does not contain enough vitamin D.
Diseases that affect the intestinal absorption of nutrients can impair the absorption of the vitamin, the most important of which are:
• Celiac disease.
• Inflammatory bowel disease.
• Cystic fibrosis.
• College problems.
Genes: There is a type of rickets that can be inherited, meaning that the disease can be passed on through your genes. This type of rickets, called hereditary rickets, prevents the kidneys from absorbing phosphate.
How is rickets diagnosed?
During the clinical examination, the doctor looks for characteristic signs of the disease, the most important of which are:
• Pain provoked by palpation in the bones of the arms, legs, pelvis, or spine.
• Delayed growth and short stature.
• muscle spasms or muscle looseness.
• Dental abnormalities, such as:
o Delayed tooth formation.
o Drilled into the enamel of the teeth.
A defect in the structure of the teeth.
• Skeletal abnormalities, including:
O skull with a strange shape, where the bones of the skull are soft so that pressure on them leads to deformation in its shape.
o Protrusions in the rib cage.
o A prominent sternum bone.
o Scoliosis of the spine.
o Pelvic abnormalities.
o Severe curvature of the legs.
o Enlargement of the wrists and ankles.
The doctor may also order some tests to help him make a diagnosis. These tests include:
• Blood tests to measure the levels of calcium and phosphate in the blood.
• X-rays of the bones, where rickets causes abnormalities in the bones that are visible on the radiograph.
In rare cases, a bone biopsy may be done, that is, the removal of a very small part of the bone that is sent to a laboratory for analysis.

What are the complications of rickets?
Low calcium levels cause cramps, convulsions, and trouble breathing. While complications are exacerbated in the case of untreated rickets in the long term, in addition to the soft and easily breakable bones, deformities of the rib cage can cause heart and respiratory problems, the most important of which is pneumonia.

What are the ways to treat rickets?
The treatment of rickets focuses on replacing the lacking vitamin or mineral in the body, which reduces most of the symptoms associated with rickets. Ask the doctor about the appropriate dose of vitamin D and calcium for the age and weight of the child, as taking them in the wrong doses can be harmful.

If skeletal abnormalities are found, the child may need braces to properly hold the bones as they grow. In severe cases, the child may need corrective surgery.

For hereditary rickets, treatment of the disease requires a mixture of phosphate supplements and large amounts of a special type of vitamin D.

Remember that prevention is better than a pound of cure, so make sure that your child eats a balanced diet appropriate for his age, and encourage him to eat more foods rich in vitamin D such as fish, liver, milk and eggs. Encourage the child to play outside the house, although prolonged exposure to the sun at peak times is linked to burns and skin cancer, but moderate exposure at appropriate times helps in healthy growth and prevention of disease. You should also make sure to take the preventive doses of vitamins and nutritional supplements that your doctor prescribes for you.

the reviewer:

Articles of Diseases : Tumors and cancers

Articles of Diseases

Chemotherapy is a drug treatment that uses strong chemical drugs to kill malignant cells in the patient’s body. This treatment relies on specific protocols depending on the tumor’s type and degree of growth and spread, using one drug or a combination of drugs at the same time.Although chemotherapy is an effective way to treat many types of cancer, chemotherapy also carries a risk of many side effects, some of which are mild, simple and treatable, while others can cause serious complications.

Why is chemotherapy used?

Chemotherapy affects cells in the process of growth and reproduction, and since cancer cells grow and multiply more quickly than most cells in the body, chemotherapy affects them much more than it affects healthy cells. Chemotherapy is used in the treatment of tumors in order to reduce the total number of cancer cells in the patient’s body to reduce the possibility of cancer spreading, and to reduce the size of the tumor and relieve its symptoms. It is also used in different stages, for example: Chemotherapy is used after surgery. After a cancerous tumor has been surgically removed, such as a lumpectomy in breast cancer, the oncologist may recommend chemotherapy to make sure that any remaining cancer cells that were not reached by the scalpel are also killed. Chemotherapy can be used before surgery to shrink the tumor so that the surgeon can easily remove it surgically, and to reduce the risk of bleeding during surgery. Chemotherapy is used as a palliative treatment in late-stage cancer to relieve symptoms and reduce pain. In addition to its important role in the treatment of cancer, chemotherapy can be used before marrow transplantation, where chemotherapy kills the patient’s marrow cells so that the body can accept the healthy transplanted marrow cells, and it can be used to treat some autoimmune diseases, but at much lower doses than those used to treat cancer To control disorders in which the body’s immune system attacks healthy cells, such as systemic lupus erythematosus or rheumatoid arthritis.

How is chemotherapy given?

There are many ways by which the chemical can be delivered to the patient’s body, and these methods vary according to the location and location of the tumor and the type of drug used, and among these methods are the following:

By injection: where drugs are delivered directly by injection into a muscle in the hip, thigh, arm, or just under the skin. By arterial: where drugs go directly into the artery that feeds the cancer through a needle or thin tube (catheter). Intraperitoneal (peritoneal): where drugs are delivered to the peritoneal cavity (abdominal cavity) that contains the viscera such as the liver, intestines and stomach, and this is done during surgery or through a tube with a special port placed by the doctor. Through a vein, the chemical goes directly into the bloodstream and into the tumor. Oral: where the patient swallows a pill or liquid containing the chemical.What are the side effects of chemotherapy?

Some of the common side effects of chemotherapy include fatigue, nausea and vomiting, low blood cell count, hair loss, and ulcers in the mouth and stomach. Hair loss and a decrease in the number of red and white blood cells during chemotherapy in most patients. The duration of side effects depends on the patient’s health and the diseases he suffers from before starting chemotherapy and the type of chemotherapy the patient receives. Most of the side effects disappear after completion of chemotherapy within a short period, but sometimes it may take months or even years for the symptoms to disappear, but some symptoms may be severe and permanent such as damage to the heart and lungs, decreased kidney function, impotence, male infertility, and infertility when In women, some types of chemotherapy may cause a second, different cancer to develop after several years.

How does the doctor decide what chemotherapy drugs to use?

This depends on the type of cancer the patient has, as some medicines are used to treat only one or two types of cancer, while there are medicines that are used for many types of cancers. The decision also depends on the patient’s other problems such as diabetes, liver and kidney problems, or heart disorders.

What are the recommendations after chemotherapy to reduce side effects?

Nausea and vomiting may be one of the most common side effects after chemotherapy, and to get rid of them, the doctor recommends eating small meals, avoiding strong smells and flavors, and chewing gum that removes the bitter taste from the mouth. It is important to avoid insomnia at night, which is a very common symptom in people with cancer, so stimulant drinks such as coffee and tea should be avoided at night. You should also eat foods rich in fiber that help soften the stool and make bowel movements more frequent to treat constipation caused by chemotherapy, and it is also important to drink water that helps hydrate the body and facilitate the movement of stool through the intestines, where doctors recommend consuming about (3) liters of water daily, especially if constipation is chronic.   the reviewer:

With the progress of science and modern diagnostic methods, the early detection of cancer program has developed, a program that enables doctors to detect the presence of many tumors and cancers early, which greatly improves the chances of treatment and recovery.Early detection programs are certain tests that look for the presence of cancer in the body in the early stages before symptoms appear. Regular early detection tests lead to early detection of breast, cervical, prostate, and colorectal (colon) cancers, which increases the chances of recovery. Lung cancer screening for some of the people most at risk of developing it.

Breast Cancer Early Detection Programs:

Early detection of breast cancer means examining a woman’s breast for cancer before signs or symptoms of the disease appear, and although breast cancer screening cannot prevent breast cancer, it can help find breast cancer early, which makes treatment easier And its results are better.

Doctors usually start with a clinical breast exam to check for lumps or changes in breast tissue, but that alone is often not enough, which causes them to order more tests, and the most important of these tests are:

Mammogram of the breast: It is a mammogram using X-rays, and is considered the best way to detect breast cancer early, making it easier to treat and deal with it before the disease has advanced enough for symptoms to appear, and regular mammograms can reduce the risk of death from cancer the breast.
Breast magnetic resonance imaging (MRI): MRI isn’t usually used routinely, but an MRI combined with a mammogram is important for screening for women at high risk of breast cancer.
Cervical Cancer Early Detection Programs:

Early detection tests can help prevent cervical cancer or find it early, and the most important of these tests are the Pap test and the HPV test.

A Pap test looks for changes in the cells of the cervix, and the test detects the presence of abnormal cells before they develop into cancer. While the HPV test looks for the presence of this virus that can cause these carcinogenic changes in the cells of the cervix.

Both tests can be done in a doctor’s office. During a Pap test, the doctor uses a plastic or metal instrument, called a speculum, to widen the vagina. This helps the doctor to examine the vagina and cervix, and collect a small number of cells and mucus from the cervix and the area around it, to send these samples later to the laboratory for examination to ensure that there are no abnormal cells as well as the absence of HPV infection.

Colorectal Cancer Early Detection Programs

Colorectal cancer often develops from polyps (abnormal growths of cells) in the colon or rectum. Early detection tests for colorectal cancer can find precancerous polyps so that they can be removed before they turn cancerous. Screening tests can also detect precancerous polyps. Early colorectal cancer also occurs early, which improves the chances of a cure.

Regular screening, starting at age 50, is key to preventing colorectal cancer. Studies recommend early detection screening for adults between 50 and 75 years of age to check for colorectal cancer, including several tests such as stool tests, colonoscopy, and CT colonography.

Prostate Cancer Early Detection Program:

Prostate cancer is the most common cancer in men, and it is important to have a clinical examination and measurement of the prostate enzyme (PSA) once a year.

The (PSA) is one of the tumor markers and it is usually elevated in prostate cancer, but its accuracy is not 100%. It may be elevated in other cases such as benign prostatic hypertrophy and prostatitis, so doing it alone is not considered sufficient without clinical examination.

Lung Cancer Early Detection Programs:

Low-dose computed tomography is the only test recommended for lung cancer. During this test, the patient lies on a table and an X-ray machine uses low-volume X-rays to make detailed images of the lungs.

Unlike previous screenings, lung cancer screening is not a routine part of an early cancer detection program for all people, but it is wise to perform LDCT in people at high risk of lung cancer such as heavy smokers who are current smokers or have quit within the past few years .

Is the early detection program for cancer effective?

The early cancer detection program is considered one of the leading and medically important programs, and it has proven its success and its ability to detect cancer early, which greatly improved the results of treatment. The early detection program for cancer is not limited to laboratory and radiological examinations. Some early cancers, especially skin cancer and testicular cancer.

Extensive studies are being conducted all over the world to improve this program, increase the efficiency of the tests used, and improve their ability to detect cases at earlier stages. These studies also aim to find ways to detect other types of cancer early, such as ovarian cancer, pancreatic cancer, testicular cancer and thyroid cancer.

the reviewer:

Many people associate diseases in general and cancers in particular with adults, and they believe that these malignant diseases infect children, but this is not always true. Some cancers tend to affect young children, including leukemia, lymphoma, especially non-Hodgkin’s lymphoma, retinoblastoma, which affects the retina, and Wilms’ tumor, which affects the kidney.

 

Leukemia is the most common type of cancer in children and adolescents, and acute lymphoblastic leukemia accounts for three quarters of cases. What is acute leukemia and why does it occur?

What is leukemia?

Leukemia is a tumor of the blood and bone marrow; It is the spongy tissue inside the bone where blood cells are made. Later, this tumor moves to the liver and spleen, and may affect the brain, spinal cord, lungs, and testicles in males.

Leukemia can occur in different forms, including acute, which develops quickly, and others chronic. It can occur in myeloid leukemia (myeloid leukemia), or in lymphocytes, which are a type of white blood cell (lymphocytic leukemia).

What we are going to talk about is acute lymphoblastic leukemia, a form of blood cancer.

What are the causes of acute lymphocytic leukemia?

Acute lymphocytic leukemia occurs as a result of a defect in the growth of bone marrow cells, where these cells continue to grow and divide abnormally at the expense of healthy cells and the production of blood cells becomes abnormal, including white blood cells, red blood cells and platelets.

Who are the people most at risk of acute lymphoblastic leukemia (ALL)?

It can affect anyone, but it is more common in children than adults, and it is worth noting that the results of its treatment in children are excellent, as most children with it recover, while the cure rates are much lower in adults.

Acute lymphoblastic leukemia affects people who have survived another cancer, especially those who have received chemotherapy or radiation, and it also affects people with Down syndrome more than others.

Acute lymphocytic leukemia tends to recur in the same family, so having a brother or sister with it increases the risk of developing the disease.

What are the symptoms of acute lymphocytic leukemia?

There are no distinct symptoms at the beginning of the disease. The child may develop a high temperature with mild flu-like symptoms, and a rash may appear in some cases. Later, the bone marrow begins to produce immature cells, and the number of red and white blood cells and platelets in the blood decreases, and some symptoms appear, such as:

Pale skin, shortness of breath, fatigue, fatigue, lack of appetite, and weight loss, which are symptoms of anemia and occur due to a lack of red blood cells.
Frequent nosebleeds, bleeding gums, bruising on the skin, or bleeding anywhere in the body such as digestive or urinary bleeding due to low platelet count.
Frequent infections with elevated temperature as a result of leukopenia.
The child suffers from bone pain due to hemorrhage under the bone crust, and in the advanced stages the tumor moves, causing tumors and masses in the brain, which leads to seizures, facial nerve paralysis, and blurring of vision. Parents may notice the emergence of behavioral disorders.

How is acute lymphocytic leukemia diagnosed?

The doctor notes by clinical examination signs of anemia, bleeding and bruises on the skin, as well as enlargements in the lymph nodes in the neck, in the abdomen, under the armpits, or in the groin, and the spleen is enlarged. In the laboratory, the complete blood count (CBC) will show a decrease in the number of red blood cells, white blood cells and platelets, and the laboratory may be able to see immature lymphocytes on the blood smear.

Bone marrow tapping is considered a confirmatory test for the presence of leukemia, as it reveals the marrow is occupied with abnormal lymphocytes, in contrast to immune thrombocytopenia (ITP) in which the puncture is normal. Puncture must be performed and read by an expert to distinguish acute lymphoblastic leukemia from many diseases that cause marrow failure such as neuroblastoma, Ewing’s sarcoma, aplastic anemia, myeloma, and others.

X-rays of the bones show abnormalities in the shape of the bone, and the doctor needs to perform a computed tomography (CT scan) to detect the tumor’s spread and access to other areas such as the chest, brain or spinal cord.

Abnormal cells appear by a cerebrospinal fluid puncture, where a small sample of the fluid that surrounds the brain and spinal cord is withdrawn by inserting a thin needle in the lower back and examining this fluid.

How is acute lymphocytic leukemia treated?

The basic principles of treatment include induction of remission so that no leukemia cells appear on the myelogram, preventive treatment of the nervous system, and continuation of supportive therapy for several years. Treatment includes:

Chemotherapy: Medicines are used to kill cancer cells.
Targeted therapy: In which drugs are used to attack specific cancer cells, this treatment has fewer side effects than regular chemotherapy.
Radiation therapy: It uses high-energy beams such as X-rays and protons to kill cancer cells.
Bone marrow transplant: It is also known as stem cell transplantation, where infected bone marrow cells are replaced with bone marrow cells taken from a healthy person after making sure of a match, or stem cells taken from the same person are transplanted.
Most children under the age of ten recover, but unfortunately the situation is worse and the probability of recovery is less in infants under two years or in adolescents and adults, or in the presence of masses of transmission to the chest or severe leukocytosis (above 100 thousand).

 

the reviewer:

The esophagus is a hollow muscular tube responsible for transporting food from the throat to the stomach. The esophagus consists of several layers. Inside the tube there is a layer of thin cells that form the lining and around it are layers of muscle. The esophagus also contains glandular cells, lymphocytes, and others. Esophageal cancer can occur when a malignant tumor forms in the lining of the esophagus. As the tumor grows, it can spread to the deeper tissues and muscles of the esophagus and may travel through the blood to distant sites in the body. What is esophageal cancer and how can it be prevented?

 

What is esophageal cancer?

Esophageal cells grow and multiply to replace the damaged cells, but in some cases the cells multiply more quickly than normal, forming a tumor. Tumors can appear anywhere along the esophagus, including where the esophagus and stomach meet. Esophageal cancer has two common types:

Squamous cell carcinoma occurs when cancer begins in the flat, thin cells that make up the lining of the esophagus. This form most often appears in the upper or middle part of the esophagus, but it can appear anywhere in the esophagus.
Adenocarcinoma occurs when cancer begins in the glandular cells in the esophagus that are responsible for producing fluids such as mucus. This type is more common in the lower part of the esophagus.
There are other less common types such as lymphoma, which arises at the expense of lymphocytes, sarcoma, which arises at the expense of muscle cells, and melanoma, which arises at the expense of pigment-producing cells.

What are the symptoms of esophageal cancer?

The tumor does not cause any symptoms at the beginning, but as the tumor grows, the esophagus narrows, causing a feeling of suffocation when eating, and difficulty swallowing food. Some other symptoms also appear, the most important of which are:

Unintended weight loss.
Indigestion.
heartburn.
vomiting.
Chest pain, where the patient complains of a burning or pressure sensation.
Chronic cough.
Hiccups.
What are the causes of esophageal cancer?

There’s no clear, specific cause of esophageal cancer, but it’s thought to be related to abnormalities (mutations) in DNA. These mutations lead to irregular and uncontrolled growth and proliferation in the cells of the esophagus. These mutations also disrupt the death of these cells at the time they should die, so the balance is disturbed, and the formation of cells becomes excessive, causing them to accumulate and become tumors.

Experts believe that irritation of the cells of the esophagus contributes to the development of cancer. Some habits and conditions that can cause irritation include:

Alcohol intake.
smoking.
Gastroesophageal reflux disease (GERD).
Having Barrett’s esophagus, a condition characterized by damage to the lining of the esophagus due to reflux.
Being overweight or obese.
Not eating enough fruits and vegetables.
Achalasia, a condition in which the muscles in the lower esophagus do not relax properly.
How is esophageal cancer diagnosed?

Diagnostic methods for esophageal cancer include:

Upper GI endoscopy: This involves using an instrument with a camera attached to a tube that goes down your throat and allows your doctor to view the lining of your esophagus to check for abnormalities and irritation.
Barium bolus: This is an X-ray imaging test that allows the doctor to see the lining of the esophagus. The doctor takes a series of X-rays after the patient swallows a contrast material called barium. The barium esophagus is clearly delineated, enabling the doctor to see the narrowing in it.
Biopsy: This is the removal of a sample of suspicious tissue with the help of an endoscope and sent to a laboratory for examination.
Doctors rely on many methods to know the extent of the spread of cancer, and thus to determine the best treatment plan, including: bronchoscopy, computerized tomography (CT scan), magnetic resonance imaging (MRI), laparoscopy or positron emission tomography (PET CT), which is one of the latest tests to assess the presence of cancer. The tumor and its spread, where the patient is given a certain radioactive substance, this substance is concentrated in the cancer cells, so the tumors appear in a black color on the image.

How is esophageal cancer treated?

Esophageal cancer treatment depends on many factors, including the stage of the cancer and the patient’s health status, and the earlier a tumor is detected, the greater the chance of success. Treatments in the early stages include endoscopic mucosal resection. This procedure is performed when the tumor is confined to the lining of the esophagus, and sometimes radiofrequency is used by a device that targets cancer cells.

Unfortunately, most cases are diagnosed after the tumor has reached an advanced stage, and then the previous treatments do not work. Rather, the patient needs difficult and complex treatments that include surgery, where surgeons work to remove part or all of the esophagus, and it is shared with radiotherapy, chemotherapy, or both. The doctor may advise resorting to modern treatments that will reduce the size of the tumor and aid its recovery, such as:

Targeted therapy: It is a modern treatment to limit the growth and spread of cancer.
Immunotherapy: It activates the body’s immune system and incites it to attack cancer cells.
Photodynamic therapy: targets cancer cells with a special laser light.
Electrocoagulation: An electric current is used to destroy cancer cells.
Cryotherapy: Cancer cells are frozen to help shrink the tumor.
How can esophageal cancer be prevented?

To date, there is no way to detect esophageal cancer early, and unfortunately, this type of cancer does not cause any symptoms in the early stages, so it is diagnosed late and treatment is difficult. Although there is no sure way to prevent esophageal cancer, there are some steps you can take to reduce your risk:

Avoiding smoking in all its forms and chewing tobacco is essential.
Limit alcohol consumption.
Eating a diet that contains plenty of fruits and vegetables and maintaining a healthy weight are effective ways to avoid esophageal cancer. To find out your ideal weight, click here.

the reviewer:

The skin, like any other organ, develops tumors, and cancers that can affect the skin include basal cell carcinoma (BCC), squamous cell carcinoma (SCC), and melanoma, and although melanoma is not the most common cancer, but it is characterized by its rapid spread and danger, as it quickly transforms From a localized tumor limited to a small patch of skin to a metastatic carcinoma. This article will cover the symptoms and causes of melanoma, how doctors diagnose it, and possible ways to prevent it.

 

What is melanoma?

Melanoma is a tumor that arises at the expense of melanin-producing cells, and melanin is the pigment that gives the skin and the iris their natural color. There are several factors that increase the risk of developing skin cancer, such as excessive exposure to the sun, light skin color, and a family history of skin cancer known as melanoma. Early diagnosis often improves treatment outcomes. For this reason, it is always advised to keep track of any changing or developing moles and to use sun protection for long periods of time, which may help a person prevent skin cancer.

What are the main symptoms of skin cancer?

Early signs and symptoms of melanoma include:

Changes in an existing mole.
Note new and abnormal growth in the skin.
If melanoma cells make melanin, then tumors tend to be dark brown or black, but some melanomas do not make melanin, so those tumors can be pink or white. Here are some indications and indications that this or that mole may be a cancerous tumor:

If its shape is irregular.
Its borders are irregular.
If their coloration is multicolored or uneven.
If the area is large.
If there is any change in size, shape or color.
If the mole is accompanied by itching or blood coming out of it.
Skin cancer can start anywhere on the skin, however the most likely areas are:

Chest and back in men.
Lower extremities in women.
neck and face.
This may be due to the exposure of these areas to the sun more than other parts of the body, and melanoma can form rarely in areas that are not exposed to the sun, such as the soles of the feet, palms and nails, or in the melanin-producing cells in the mucous membranes that line the alimentary canal, mouth, nose, or Urinary tract or vagina. Sometimes, the skin appears normal even though the melanoma has begun to grow and develop.

As the disease progresses, cancer cells grow and multiply. They travel first to nearby lymph nodes, causing enlargement of the nodes, and then move to distant organs, causing tumors in the brain, lung or liver.

What causes melanoma?

Normally, new healthy skin cells push old skin cells to the surface, where they are damaged and die. DNA damage within melanocytes can cause new skin cells to grow abnormally, and as these cells build up, a tumor can form.

It is not yet clear why DNA damage in skin cells may be due to a combination of genetic and environmental factors, the most important of which is exposure to ultraviolet (UV) rays. The most important factors that contribute to the development of melanoma are:

Skin tone: Melanoma tends to occur in people with fair skin, especially those with blond or red hair, and those with freckles.
People who have many moles.
Age factor: The risk of developing skin cancer increases with age, as the average age at diagnosis is 63 years, although it is one of the most common types of cancer among young people.
Exposure to the sun or ultraviolet rays such as tanning salons.
Weakened immune systems such as AIDS patients, or patients taking immunosuppressants after an organ transplant.
How we can diagnose the disease?

The patient needs a comprehensive examination of the skin. Most of us will often have between 10 and 50 moles by the time we reach the age of 50. A normal mole usually has a uniform color and clear borders, and can be round or oval and of small diameter. A good skin exam involves looking in less visible places, such as between the buttocks, the genitals, the palm of the hand, and under the nails and scalp. Doctors often need to do more tests and blood tests to confirm the diagnosis. These tests include:

Skin biopsy: It is the only way to confirm the diagnosis of skin cancer. For a biopsy, a sample of the skin is removed, if possible. The entire suspicious area must be removed, and the tissue is sent to the laboratory for examination under a microscope.
Lymph node biopsy: If the diagnosis of melanoma is confirmed, the doctor will need to know if the cancerous cells have spread.
Imaging tests: Imaging tests are used to find out if the cancer has spread outside the skin to other parts of the body. The most important of these are computed tomography (CT scan), magnetic resonance imaging (MRI) and positron emission tomography (PET Scan). Positron emission tomography is a newer procedure and is done by injecting a small amount of radioactive glucose into a vein. Cancer cells absorb more glucose, so they appear as dark spots.

What are the ways to treat melanoma?

Treating melanoma confined to the skin is easy, but treating metastatic cases is complex and depends on a combination of surgery, chemotherapy, radiotherapy, and immunotherapy.

What are the ways to prevent melanoma?

Exposure to the sun is vital, as it provides the body with its need of vitamin D. But exposure to the sun at peak times increases the risk of heat stroke and burns in the short term, and it also increases the risk of skin cancer. It is important to avoid exposure to the sun in the afternoon, wear cotton clothes, and put a sunscreen of not less than 30 degrees before exposure to the sun, and repeat its application every two hours, and after showering, sweating or swimming.

the reviewer:

The cells of the body grow and multiply in order to grow in children and replace lost and damaged cells in adults, but in some cases the body loses its control over cell proliferation, and a large mass of accumulated cells arises that we call cancer. Cancer can affect any organ of the body, and when it affects the kidney, we call it kidney cancer (Kidney Cancer) and it has many types depending on the cells on which it arises, and we will talk about kidney cancer in some detail.What is kidney cancer?Kidney cancer is a disease in which kidney cells become malignant (cancerous) and grow out of control and form a tumor. Almost all kidney cancers first appear in the lining of the small tubes in the kidney that filter blood. This type of kidney cancer is called renal cell cancer, which is diagnosed at stage Early in the disease, Wilms’ tumor is another type of kidney cancer that may affect children under 5 years of age, but it is rare.

 

The good news is that most kidney cancers are found before they spread to distant parts of the body. In 85% of cases, kidney cancer is found by chance when a CT scan or magnetic resonance imaging (MRI) is performed for a reason other than the kidney. Cancers that are caught early are easy to treat successfully.

What are the causes of Kidney Cancer?

It is not clear what is the exact cause of kidney cancer, and doctors believe that kidney cancer begins when some kidney cells acquire mutations in their DNA, which causes them to grow and divide rapidly, and these accumulated abnormal cells form a tumor that may extend beyond the kidney and spread to parts far from the body.

There are many factors that increase the risk of kidney cancer, the risk of developing increases in the elderly with age, and smokers are more likely to develop kidney cancer than non-smokers, but this risk decreases after quitting smoking, and people with chronic kidney failure Especially after long-term dialysis, the risk of kidney cancer increases in people who suffer from high blood pressure or obesity, and do not forget the role of some genetic syndromes, family history of renal cell cancer, and exposure to some toxic substances in the workplace, especially some pesticides.

The presence of risk factors does not mean that a person will inevitably develop kidney cancer, and cancer may develop in the kidney in the absence of these factors.

What are the symptoms of Kidney Cancer?

In many cases, the patient may not have any early symptoms of kidney cancer, but as the tumor grows larger, symptoms may appear, and these symptoms include: blood in the urine, feeling a lump in the abdomen or flank, loss of appetite, severe pain that does not go away easily, Weight loss without a known cause, anemia, swelling in the legs and arms when the kidney function fails in the advanced stages of the tumor and its inability to excrete excess fluid from the body.

Since kidney cancer may spread to other parts of the body, this may cause different symptoms such as shortness of breath, coughing up blood, or bone pain, depending on the location of the cancer metastases when spreading in the body.

How is Kidney Cancer diagnosed?

Diagnosing kidney cancer requires knowledge of the patient’s medical and family history and a complete physical examination, in which the doctor looks for a lump or swelling in the abdomen. Some of the tests that may be used to detect kidney cancer include:

Blood tests include a complete blood count (CBC) to assess the status of red blood cells, white blood cells and platelets, where anemia can occur in some cases, while the number of red blood cells increases as a result of an increase in erythropoietin, a hormone produced by the kidneys that stimulates the production of red blood cells. The doctor also requests an assessment of the functions of the college.
Urinalysis, which usually detects the presence of red blood cells in the urine.
Ultrasound of the kidney and abdomen (echo) to measure the size and shape of the kidneys and to detect tumors, if any.
Ultrasound of the urinary system. In this test, a contrast material is injected into a vein in the body, allowing the kidneys to be seen more clearly using X-rays, which helps find the tumor or blockage.
In some cases, the doctor needs more accurate tests, such as a computed tomography (CT) scan or magnetic resonance imaging (MRI) of the abdomen, which allows to know whether the cancer has spread outside the kidney.
How is Kidney Cancer Treated?

Patients who are still in the early stages of the disease usually have a great chance of recovery, as the treatment aims to surgically remove the affected part of the kidney, and this does not affect the patient’s life after surgery, as the person can survive with part of the kidney as long as it is still It works, while the patient needs dialysis if the surgery involves both kidneys, and he may need to transplant a new kidney.

But if surgery cannot completely eradicate kidney cancer, the doctor may suggest another option to help destroy the tumor, such as radiation therapy or biological therapy.

 

the reviewer:

Hodgkin’s disease is a type of tumor that affects the lymphatic system and leads to enlargement of the lymph nodes in the body. Fortunately, this tumor responds well to treatment if it is detected and treated early. What is Hodgkin’s disease, and what are its symptoms?What is Hodgkin’s disease?

 

Hodgkin’s disease, also called Hodgkin’s disease or Hodgkin lymphoma, is a type of tumor that affects the lymphatic system. The lymphatic system consists of groups of lymph nodes scattered throughout the body under the jaw, neck, chest, armpit and groin (the area where the thigh meets the abdomen) connected to each other by lymphatic vessels. There are also lymphoid cells in the spleen, tonsils, bone marrow, digestive system, and others. These nodes filter the fluid passing through them to get rid of waste and fight infections, so when there is any inflammation in the body, the group of nodes in this part swells and swells, but it returns to its normal size and position after the inflammation is gone.

In some cases, these nodes grow abnormally, lose their ability to work and fight diseases, and their cells multiply in excess and may start attacking and invading healthy tissues, and this is what we call lymphoma, i.e. lymphoma, and it has two basic forms: Hodgkin lymphoma and Non-Hodgkin lymphoma. .

Hodgkin’s disease may come in two types, either classic Hodgkin’s disease or autosomal dominant lymphoma (NLPHL). Histological analyzes can determine the pattern of cells and predict their behavior and aggressiveness, which is useful in determining the best treatment plan.

What are the causes of Hodgkin disease?

The exact cause of Hodgkin’s disease is still unknown, but studies accuse some factors, especially genetic mutations. Hodgkin’s disease affects males more than females, and Hodgkin’s disease may occur at any age, but it is most common between 15 and 35 years, and after 55 years. Among the possible causes that may lead to disease:

Viruses: Hodgkin’s disease has been linked to some viruses, specifically the Epstein-Barr virus (EBV).
Genetic factor: Same-sex siblings, as well as identical twins of a person with Hodgkin’s tumor, are at greater risk than others of developing the disease, and if the father suffers from Hodgkin’s disease, the children are also at greater risk of developing it.
Environment: Having fewer siblings, premature birth, and fewer playmates are associated with an increased risk of Hodgkin’s disease, possibly due to lack of exposure to bacterial and viral infections at an early age.
What are the symptoms and signs of Hodgkin’s disease (Hodgkin Lymphoma)?

Some of the patient’s lymph nodes become swollen, and these swollen nodes form a lump under the skin, and this lump is usually not painful. The patient may notice them in one or more of the following places:

on the side of the neck.
in the armpit.
In the groin, which is the area where the thigh meets the abdomen.
Other symptoms of Hodgkin’s disease include:

Night sweats.
skin itching;
An increase in body temperature.
Fatigue and general fatigue.
Unintended weight loss.
Respiratory symptoms such as persistent cough, difficulty breathing, chest pain.
How is Hodgkin’s disease diagnosed?

To diagnose Hodgkin’s disease, the doctor often takes a detailed medical history from the patient and conducts a clinical examination that clearly reveals the enlarged nodes and their locations and size. The doctor may also be able to palpate the enlarged spleen, and then the doctor will also order certain tests so that he can reach the appropriate diagnosis. The most common of these tests are:

Blood tests such as a complete blood count (CBC): A complete blood count measures the number of red and white blood cells and the level of platelets. For example, when these components are reduced, this indicates damage to the bone marrow due to the tumor reaching it.
A lymph node biopsy, which involves removing a piece of lymph node tissue to test for abnormal cells.
Imaging tests, such as computed tomography (CT scan), magnetic resonance imaging (MRI), or positron emission tomography (PET-CT). Imaging tests help evaluate the extent of the tumor and are important for determining a treatment plan.
Immunophenotyping, to determine the type of lymphoma cells present.
Pulmonary function tests to determine how well the lungs are working.
Echocardiogram to determine how well the heart muscle is working.
Bone marrow biopsy, which involves removing and checking the bone marrow to see if cancer has reached the bone marrow.
These analyzes are useful in determining the type of lymphoma present, and in estimating its spread, where the degree of lymphoma is measured on a scale of four degrees. The first degree refers to a disease confined to a specific lymph node group (for example, the neck nodes group), while the fourth degree refers to a tumor that has spread outside the lymphatic system so that It affects other organs such as the liver, lung or bone marrow.

How is Hodgkin’s disease treated?

Treatment for Hodgkin’s disease depends on the type of cancer cells and the stage of the disease, and chemotherapy and radiotherapy are the main treatment options.

Radiation therapy uses high-energy rays to destroy cancer cells, while chemotherapy involves the use of drugs that can kill cancer cells. Chemotherapy drugs can be given orally or intravenously, depending on the drug and treatment plan that the doctor deems appropriate.

Immunotherapy or stem cell transplantation can also be used if the condition does not respond to chemotherapy or radiation, where cancer cells are replaced with stem cells capable of differentiating to form different types of cells.

After treatment, doctors usually want to monitor the patient’s condition on a regular basis, and it is important to keep all appointments and follow the doctor’s instructions regarding treatment.

What are the risks of treatment?

Treatments used for Hodgkin’s disease can have long-term side effects and may increase your risk of developing other serious medical conditions. including:

Other cancers.
Infertility Infertility may occur in males as in females.
Thyroid problems.
Lung tissue damage.
Decreased white blood cell count, which leads to decreased immunity and easy infection.
A lack of platelets, which leads to the occurrence of bleeding easily.
Doctors stress the importance of regular mammography, heart disease checks, keeping up with vaccinations, and avoiding smoking.

the reviewer:

The pancreas is a 15 cm long organ located behind the stomach in the back of the abdomen, near the gallbladder and contains glands that secrete pancreatic juices, hormones and insulin. These glands are divided into two types:The exocrine glands are the glands responsible for the synthesis and secretion of digestive enzymes that reach the intestine through the pancreatic duct and help digest fats, proteins and carbohydrates. These glands make up most of the pancreas. If these enzymes are released within the pancreas, they cause necrosis in its cells.
The islets of Langerhans are glands that release the hormones insulin and glucagon into the bloodstream, where they regulate blood sugar levels. When these two hormones don’t work properly, the result is often diabetes.
Cancer can affect any part of the pancreas, and symptoms vary slightly depending on which part is affected.What are the causes of pancreatic cancer?

 

This type of cancer occurs when abnormal cells begin to grow inside the pancreas and form tumors. Normally, healthy cells multiply to compensate for the deficiency as a result of cell death or damage for some reason, and this occurs in a balanced and accurate manner. In the case of cancer, there is an increased amount of abnormal cell production, and these cells eventually take over the healthy cells.

While doctors and researchers do not know what causes changes in cells, they do know some common factors that may increase a person’s risk of developing this type of cancer, including:

Lifestyle: The risk of infection increases in smokers, people who drink alcohol in large quantities, or people with obesity, and a sedentary lifestyle, lack of exercise and eating meals rich in fat increases the rates of infection.
Long-term exposure to pesticides and chemicals.
Pancreatic cancer is associated with some diseases, the most important of which are: diabetes, cirrhosis of the liver, or chronic inflammation of the pancreas.
In some cases, cancer is hereditary, and this occurs when the genetic material that controls the process of cell proliferation is damaged. In these cases, a person inherits a predisposition to cancer, meaning that the possibility of infection is higher than others. This includes not only pancreatic cancer, but also colorectal cancer, skin cancer, breast cancer and ovarian cancer.
What are the symptoms of pancreatic cancer?

There are usually no early signs of pancreatic cancer. Even as the cancer grows, some symptoms can be deceptive and resemble those of common diseases, so pancreatic cancer is often diagnosed in the advanced stages of the disease. The most common symptoms include:

Anorexia.
Unintended weight loss.
Abdominal or back pain.
blood clots;
Depression.
The growth of the cancerous tumor leads to blockage of the collecting duct, which is the duct that transports the secretions of the pancreas and liver to the intestines. The patient is unable to digest food well, causing large amounts of fat in the stool, causing diarrhea. The juices also accumulate in the liver, causing jaundice (yellowing of the skin and eyes). The patient will suffer from additional symptoms when the cancer spreads, and these symptoms are related to the area to which the cancer has spread, noticing fractures if it moves to the bones, coughing if it spreads to the lung, and so on.

How is pancreatic cancer diagnosed?

Early diagnosis greatly increases the chances of recovery. That’s why it’s best to see your doctor if you have any symptoms that don’t go away or that recur regularly. To make a diagnosis, your doctor will review your symptoms and medical history. He may order one or more tests to check for pancreatic cancer, such as:

Order a computerized tomography (CT) scan or magnetic resonance imaging (MRI) scan to obtain a complete, detailed picture of your pancreas.
An endoscopic ultrasound is requested, where a thin flexible tube with a camera is inserted, in order to take pictures of the pancreas through the stomach. These images are more accurate than transabdominal ultrasound because they allow you to see the pancreas up close.
A biopsy or tissue sample is taken from the pancreas.
Ordering blood tests to detect whether a tumor index CA 19-9 is present, which can indicate pancreatic cancer. This test is an indicator of the presence of cancer, but it is not sufficient to make a diagnosis, but it is useful for follow-up treatment and evaluation of its success.
How is pancreatic cancer treated?

Treatment for pancreatic cancer depends on the stage of the cancer, and it has two goals: to kill cancer cells and prevent the disease from spreading. Possible types of treatment include:

surgery:
The surgery involves removing part or all of the pancreas, and the patient develops diabetes after removing the entire pancreas because he has lost the insulin-producing cells. Depending on the location and size of the tumor, the surgeon often has to remove other abdominal organs such as part of the spleen, or part of the stomach along with the duodenum (the first piece of the small intestine) and lymph nodes. These operations are considered difficult and complex operations, which commonly cause complications, the most important of which are weight loss, intestinal obstruction and abdominal pain.

This surgery can kill the original tumor, but it won’t remove cancer that has spread to other parts of the body, so surgery isn’t suitable for people with metastatic pancreatic cancer.

Radiation therapy:
Other treatment options should be considered once the cancer has spread beyond the pancreas. Radiation therapy uses X-rays and other high-energy rays to kill cancer cells.

Chemotherapy:
In some cases, your doctor may combine other treatments with chemotherapy, which uses cancer-killing drugs to help prevent the future growth of cancer cells.

Targeted therapy:
This type of cancer treatment uses drugs or other methods to specifically target cancer cells and destroy them. These medications are designed not to harm healthy or normal cells.

How can pancreatic cancer be prevented?

There is no specific way to prevent pancreatic cancer, and there are no tests or medical procedures capable of early detection until today. However, avoiding certain practices may reduce the risk. This includes the following:

Quit Smoking.
Maintain a healthy weight.
Doing exercise.
Eat plenty of fruits, vegetables and whole grains.
Eat less red meat.

the reviewer:

Cancer occurs when abnormal cells in the body multiply uncontrollably, and this may happen at any age, but some types of cancers are characterized by their appearance in childhood, including Wilms tumor.What is a Wilms tumor?

 

Wilms’ tumor is a rare type of kidney tumor that particularly affects children, and is also known as renal glioblastoma. Most cases are diagnosed in early childhood between the ages of one and four years and become less common after the age of five.

Wilms’ tumor is usually found in one kidney, but in some cases it can be detected in both kidneys at the same time, and this tumor is characterized by its ability to spread through the blood vessels so that it gives metastases to distant places at an early time, so it is important to diagnose and start treatment early before metastases occur.

What are the causes of Wilms tumor?

It is not clear what exactly causes a Wilms tumor, and so far researchers have not found any clear links between Wilms tumor and environmental factors such as drugs or chemicals.

Wilms’ tumor is more likely to occur in females than in males, and certain genetic factors may increase the risk of developing it. Also, children with certain birth defects are more likely to develop Wilms’ tumor, such as congenital absence of the iris, cryptorchidism (non-descent of the testicle after birth), hypospadias, small head size and hemispherical asymmetry.

What are the symptoms of a Wilms tumor?

Often this tumor grows very quickly before causing any symptoms and children may look healthy, act and play normally, but most children with Wilms tumor have one or more of these symptoms: bloating and abdominal pain, hematuria, and the mother often notices a mass Large in the abdomen.

Some children complain of other less common symptoms such as fever, nausea, loss of appetite, and constipation. Wilms’ tumor can sometimes cause a rise in blood pressure that causes headache and shortness of breath, and in rare cases the pressure rises enough to cause problems such as bleeding inside the eye and altered consciousness.

Most symptoms are common, and parents may think there is another, simpler and less serious cause. But the presence of the mass during the clinical examination by the doctor is what guides the diagnosis.

How is a Wilms tumor diagnosed?

After a complete examination of the child, the doctor will likely want to know if a family member has had cancer and urinary problems in the past, and then order several tests to confirm the diagnosis, such as a blood test to check red and white blood cells and kidney function, and a urinalysis to look for the presence of blood in it.

Ultrasound imaging is considered the key to diagnosis, as it confirms the presence of a mass at the expense of the kidney and determines the state of the corresponding kidney, and computed tomography (CT Scan) has replaced intravenous imaging these days, as it confirms the presence of a solid tumor at the expense of the kidney and reveals The presence of transitions in the lymph nodes or liver transitions or any injury to the adjacent visceral organs, and a computed tomography of the chest is performed at the same time, which dispenses with a simple image of the chest to detect pulmonary transitions.

A biopsy (removing a tissue sample from a tumor) is not routinely done, and is recommended in some cases, at which time an echo-guided or CT biopsy is performed.

How is a Wilms tumor treated?

The treatment of Wilms tumor is to completely surgically remove the tumor. The surgeon may be able to do this by removing part of the kidney when the tumor is very small, but in most cases he has to remove the entire kidney and the child can then lead a completely normal life with one healthy kidney. Surgical treatment also includes pulmonary and hepatic transpositions.

When the tumor affects the kidneys, surgeons prefer to remove the tumor while keeping parts of the kidneys, but when the tumor is very large, the surgeons may have to remove the kidneys, and then dialysis must be performed continuously until a kidney is secured from a donor to perform the kidney transplant.

Wilms’ tumor is sensitive to chemotherapy such as actinomycin D or anthracycline. This chemotherapy is used 2-3 weeks before surgery and causes a dramatic reduction in the size of the tumor, thus making the surgery easier and less risky.

No procedure can be followed to prevent Wilms’ tumor, but if a child has risk factors, the doctor may recommend periodic kidney ultrasounds to help detect the tumor in its early stages, which greatly improves the chances of successful treatment.

the reviewer:

Tumor markers are one of many modern tests that can help a doctor predict or track the progression of treatment for a cancerous tumor. Doctors order these tests widely, so what are they and why are they done?What are tumor markers?

 

Tumor markers are proteins secreted by the cells of the body, usually in very small amounts, but their quantity increases significantly in the presence of a cancerous tumor. There are dozens of these proteins in the body, and some of them are associated with a specific tumor, but others are elevated in response to more than one type of cancer, and may be elevated in healthy cases that are not related to tumors.

Why might I need a tumor marker test?

Doctors may order tumor marker tests to find out if a patient has cancer. These tests can also help doctors learn more about cancer, which helps them develop an appropriate treatment plan for the patient.

After starting treatment, tumor markers drop significantly when the patient improves, but they rise again if the tumor relapses or the tumor spreads, so they help doctors evaluate the effectiveness of treatment, the need to adjust treatment plans, and may also be used to find out if the cancer has returned after treatment is completed.

Some markers have value in detecting tumors, for example the PSA test is useful in early detection of prostate cancer.

How is a tumor marker test performed?

There are different ways to test for tumor markers. Blood tests are the most common type of tumor marker test. Urine tests or biopsies may be used to check for tumor markers. A biopsy is a simple procedure that involves removing a small piece of tissue for testing.

What are the types of tumor markers?

There are dozens of tumor markers, and which one to take depends on your medical history and symptoms. Here are some of the most common types of tumor markers:

CA 125 (Cancer Antigen 125) test. This test is used to determine the effectiveness of ovarian cancer treatment, but it is normally elevated in women who are pregnant or have fibroids or endometriosis.
CA 15-3 and CA 27-29 tests. These tests are performed on a sample of the patient’s blood and are used to evaluate the effectiveness of breast cancer treatment in advanced cases. In the event that breast cancer is diagnosed, samples of cancer cells are taken and other tests are performed to determine the treatment plan and to determine how well the cells respond to hormonal therapy.
PSA (Prostate-Specific Antigen) test: This test is used in cases of prostate cancer, to detect cancer early, monitor treatment effectiveness, and see if the cancer has returned after treatment. However, this analysis increases in healthy cases such as benign prostatic hypertrophy or prostatitis, which makes it not possible to rely on it alone for the diagnosis of cancer.
C19-9: It is elevated in many digestive cancers such as stomach cancer, pancreatic cancer, colon cancer and gallbladder cancer. But it is elevated in many healthy conditions such as thyroid disease and pancreatitis.
CEA test: It is used in cases of colorectal cancer, lung cancer, thyroid cancer, stomach, pancreatic, breast and ovarian cancers.
AFP is elevated in liver cancer, ovarian cancer, and testicular cancer, but elevated in viral hepatitis and pregnancy.
Will I need to do anything to prepare for the test?

You usually don’t need any special preparation for a blood or urine test. If you’re having a tissue biopsy, you may need to fast for several hours before the procedure.

What do the results of these tests mean?

The results of tumor markers are useful in all stages of tumor diagnosis and treatment, and their most important uses are:

Early detection of tumors: Most of these markers are not accurate enough, and are elevated in many healthy cases, which may raise unnecessary concerns in many people. Therefore, tumor markers are used in specific cases, such as early detection of prostate cancer, or screening for the presence of the disease in people who are predisposed to developing some cancers.
Aid in diagnosis: Tumor marker analyzes can provide important information that helps distinguish a tumor from other diseases that give similar symptoms, but tumor markers are not a substitute for radiographic examinations or biopsy.
Determining the stage of the tumor: The determination of the stage of the tumor depends on the extent of its spread, and tumor markers are one of the methods of assessing this spread, but they are not sufficient alone, so the results must be studied in conjunction with other examinations.
Some tumor markers indicate the degree of malignancy and aggressiveness of the cells, which helps assess the severity of the disease.
Tumor marker values ​​decrease when the disease improves and rise when the disease relapses, which helps in monitoring the patient’s improvement and assessing the effectiveness of treatment and the need to adjust treatment plans.
Tumor marker tests can be very useful, but they cannot be relied upon alone in diagnosing and treating cancer. Tumor marker results should be evaluated with great care to avoid any errors. The most important weaknesses of tumor markers are:

In healthy conditions such as prostatitis, markers may rise, causing the patient to panic.
Some people with cancer do not show positive results for tumor marker tests.
There are no oncogenic markers for all types of cancer.
It must be remembered that diagnosing cancer and determining its stage is necessary to determine the appropriate treatment plan for the patient, so we must regret relying on tumor markers alone, but rather study their results with the results of laboratory analyzes, radiological investigations and biopsy to reach an accurate diagnosis.

the reviewer:

Stomach cancer is characterized by the growth of cancerous cells within the lining of the stomach. This type of cancer is difficult to diagnose because most affected people do not usually have symptoms in the early stages. Although stomach cancer is rare compared to other types of cancer, the biggest risk of this disease is that it is difficult to diagnose. Since stomach cancer does not cause any early symptoms, it remains undiagnosed until it has spread to other parts of the body, making it difficult to treat.What are the causes of stomach cancer (Stomach Cancer)?

 

The stomach (along with the esophagus) is part of the upper digestive tract and is responsible for digesting food and then moving nutrients to the rest of the digestive organs, called the small and large intestines. Stomach cancer occurs when normal, healthy cells in the upper digestive tract become cancerous and grow out of control, forming a tumor. This process occurs slowly, as stomach cancer tends to develop over many years.

Stomach cancer risk factors:

There is no clear and known cause for stomach cancer, but some diseases and factors may increase the risk of stomach cells developing into cancerous cells, the most important of which are:

Lymphomas (a group of blood cancers).
Helicobacter pylori infection (a common stomach infection that can sometimes lead to gastritis or peptic ulcers).
Tumors in other parts of the digestive system.
Stomach polyps (abnormal tissue growths that form on the lining of the stomach).
A diet poor in vegetables and fruits and rich in processed, smoked and salted foods.
smoking.
Having a family history of stomach cancer.
GERD increases the risk of developing cancer in the area where the stomach and esophagus connect.
What are the symptoms of stomach cancer (Stomach Cancer)?

There are no early signs and symptoms of stomach cancer. Unfortunately, this means that people often don’t know they have a problem until the cancer has reached an advanced stage.

Some of the most common symptoms of advanced stomach cancer include:

Nausea and vomiting.
frequent heartburn;
Loss of appetite, sometimes accompanied by sudden weight loss.
Constant swelling.
Early satiety (feeling full after eating only a small amount).
Digestive bleeding: Light digestive bleeding may not be visible to the naked eye, and stools may appear black because the bleeding takes hours to reach from the stomach to the rectum.
Anemia due to gastrointestinal bleeding.
a.
Exhaustion.
Stomach pain, which may get worse after meals.
How is Stomach Cancer diagnosed?

Further diagnostic tests should be done if your doctor suspects that you have symptoms that suggest stomach cancer. Diagnostic tests look for suspected tumors and other abnormalities in the stomach and esophagus. These tests include:

General blood tests to assess the presence of anemia.
Tumor markers: CA 19-9 The value of this protein in the blood increases in the presence of stomach cancer, but it cannot be relied on for diagnosis, as it rises in the presence of other cancers in the digestive system such as colon cancer and pancreatic cancer, and it may rise in diseases that are not It is related to tumors such as cirrhosis of the liver and gallstones. Tumor markers are important in the follow-up of the patient after treatment, as they decrease if treatment is successful, and rise if there is a recurrence.
Upper GI endoscopy: A thin tube equipped with a camera is passed down the throat and into the stomach, where the doctor can see the inner lining of the stomach and detect any abnormal areas. Gastrointestinal endoscopy is useful for taking biopsies from suspicious areas and sending them for histological analysis.
Imaging tests: such as a computerized tomography (CT) scan.
How is Stomach Cancer treated?

Your exact treatment plan depends on the origin and stage of the cancer, and your age and general health also play a role. Most patients require some form of surgery to eradicate the disease, and surgery is often combined with chemotherapy or radiation.

Chemotherapy: It can be given before surgery to help shrink the tumor, so that it is easier to remove. Chemotherapy can also be used after surgery to kill any remaining cancer cells. Chemotherapy is often combined with radiation therapy and may be used alone in advanced patients to help relieve signs and symptoms.
Radiation therapy: Radiation therapy can be used before surgery to shrink a tumor so that it is easier to remove, and it can be used after surgery to kill any remaining cancer cells.
Surgery: Surgery is the cornerstone of stomach cancer treatment. It aims to remove the entire cancer with a margin of healthy tissue, if possible, and nearby lymph nodes are also removed. Surgery options include:
Resection of early stage tumors of the stomach lining.
Resection of part of the stomach.
Resection of the entire stomach.
Resection of lymph nodes to look for cancer.
Surgery to relieve symptoms and signs.
Immunotherapy, such as vaccinations and medications.

the reviewer:

Colon cancer is called the silent killer, and it usually affects the elderly, but it can occur at any age. It is the most common cancer in men, and the second cancer after breast cancer in women. Despite the development of methods for early detection of cancer, deaths are still high due to the lack of awareness of this disease. Therefore, medical authorities and institutions working in the field of cancer have dedicated the month of March of each year to raise awareness of colon cancer and the benefits of early detection.

 

What is colon cancer?

Colon cancer is cancer that begins in the end parts of the intestine, ie in the colon or rectum. The disease usually begins as small, noncancerous (benign) collections of cells called polyps that form inside the colon, but over time, their cells develop into cancerous cells.

What are the causes of colon cancer?

It is still unknown why healthy polyps turn into cancerous tumors, but it is believed that a mutation plays a role, so the disease is more common in families than others. Inflammatory colon diseases such as Crohn’s disease and ulcerative colitis also predispose to colon cancer.

Colon cancer tends to affect some people more than others, as it is more common in people over fifty, or who have a previous history of colon cancer. Lifestyle also affects the rate of infection, as the risk of infection increases for various reasons, including:

Being overweight or obese.
smoking.
Drinking alcohol in large quantities.
Type 2 diabetes mellitus.
sedentary lifestyle
Follow a diet rich in processed foods or red meat.
What are the symptoms of colon cancer?

Colon cancer may not show any symptoms, especially in the early stages. Minor symptoms such as constipation or diarrhea, changes in the shape or color of stool, digestive bleeding, excessive gas, and abdominal pain may appear.

Symptoms of colon cancer are more noticeable in the later stages, when the patient complains of extreme fatigue, weight loss, a feeling that the abdomen is full, and vomiting may occur.

Colon cancer tends to spread and move to distant areas if diagnosis and treatment is delayed. Symptoms related to the site of transmission appear, such as bone fractures, difficulty breathing, jaundice, swelling of the hands and feet, and its transmission to the brain causes brain tumors that manifest as chronic headaches and blurred vision.

What are the types of colon cancer?

There are different types of colon cancer, depending on the type of cancer cells and where they form. The most common type of colon cancer is adenocarcinoma (96% of cases), which forms within the mucosal cells of the rectum or colon.

Less common colon cancers include lymphomas, which may form in the lymph nodes, and sarcomas, which may form in elastic tissue, among others.

How is colon cancer diagnosed?

When he suspects symptoms of colon cancer, the doctor will take information about your medical and family history, and then perform a clinical examination, including an abdominal exam and a rectal exam, to determine the presence of lumps or polyps. Helpful examinations ordered by the doctor include:

Blood tests: Although there is no specific blood test to diagnose colon cancer, it is important to perform a liver function and complete blood count to rule out other diseases and disorders that cause similar symptoms.
CEA, a chemical secreted by colon cancer cells that causes it to rise in the blood. CEA may be elevated in many conditions, including pancreatic cancer, breast cancer, lung cancer, ovarian cancer and thyroid cancer. It also rises in other cases, such as pancreatitis and cirrhosis of the liver, and may rise in smokers. Therefore, it cannot be relied upon to diagnose the presence of the tumor, but it is considered very useful for follow-up and knowledge of the extent of improvement and response to treatment.
Colonoscopy: This involves the use of a long tube with a small camera. This procedure allows the doctor to see inside the colon and rectum to look for anything abnormal, and biopsies may be taken during endoscopy for laboratory examination.
X-rays: Your doctor may order a simple x-ray using barium, which is a darkening material on the x-rays. The doctor inserts the barium into the intestine through an enema, and an image is made, and the barium clearly draws the inner surface of the intestine.
After establishing the diagnosis, a computerized tomography (CT) scan of the chest, abdomen and pelvis should be performed to determine the extent of the tumor’s spread, and to determine the optimal treatment plan.

How is colon cancer treated?

Colon cancer treatment depends on a range of factors, including age, general health, and extent of the tumor. In general, surgery is the first line of treatment. In the early stages, polyps may be sufficient to remove, and some patients may need to remove part of the colon or rectum. The surgeon can attach the healthy colon to the rectum, and if he is unable to do so, he will perform a colostomy, which is an opening in the abdominal wall to remove waste.

Chemotherapy is commonly used to kill any cancer cells that remain after surgery, thus reducing recurrence. In other cases, radiotherapy or medication may be used.

What are the methods of early detection of colon cancer?

Studies indicate that diagnosing colon cancer early gives excellent chances of recovery, and early detection programs aim to diagnose its presence in its early stages, and to identify and diagnose the presence of polyps before they turn into cancer. Doctors recommend that these polyps be removed prophylactically.

One of the most important early detection methods for colon cancer is to perform fecal occult blood analysis, which is an analysis that shows very small amounts of blood that are not visible to the naked eye, and colonoscopy. Colonoscopy is done once every 10 years, and your doctor may order it every five years if you’re at risk for cancer, especially if you have close relatives with colon cancer, Crohn’s disease or ulcerative colitis.

the reviewer:

The testicles are part of the male reproductive system. They are located in the scrotum (a sac of skin under the penis) outside the body. They are glands that produce sperm important in reproduction and male hormones. Cancer can arise at the expense of the testicle. Testicular cancer is a rare tumor.What is testicular cancer?

 

Testicular cancer is cancer that arises in one or both testicles. It often begins with changes in the gonads (the cells in the testicles that produce sperm). Genital cell tumors account for more than 90% of testicular cancers.

Testicular cancers can be divided at the expense of reproductive cells into two main types: seminal tumors, which grow very slowly and usually remain in the testicles without spreading, and non-sperm tumors, which are the most common form of testicular cancer, which grow rapidly and may spread to other parts of the body.

For those who suffer from early-stage testicular cancer, the five-year survival rate is greater than 95%, and the death rate is constantly declining due to the increased health awareness, and the development of treatment methods.

What are the causes of testicular cancer?

Testicular cancer occurs when healthy cells in the testicle change. In some cases, abnormalities appear in some cells, making their growth out of control. These cancerous cells continue to divide even when new cells are not needed, and the accumulated cells form a mass in the testicle, which is testicular cancer.

There are many factors whose presence raises the risk of testicular cancer, such as the disappearance of the testicle, or what is known as an emigrant testicle, as in the normal case the testicles are formed in the fetus in the abdominal area and then descend into the scrotum before birth. Men who have an ectasia of the testicles are more prone to testicular cancer than men whose testicles are normally located, and the risk remains high even if the testicle is surgically transferred to the scrotum.

The risk of testicular cancer also increases if a family member has it. Testicular cancer tends to occur in young adults and adolescents, but it can occur at any age.

What are the symptoms of testicular cancer?

Some men have no obvious symptoms when testicular cancer is diagnosed. Symptoms when they do appear may include: a painless lump in the testicle (the most common symptom), a swollen testicle with or without pain, fluid accumulation in the scrotum, pain in an upper area Thigh or lower abdomen, sometimes breast enlargement.

It is important to remember that testicular cancer tends to spread quickly, but if it is diagnosed and treated early, the results are excellent, so you should consult your doctor if you have any symptoms that last more than two weeks.

The specialist doctor will perform tests to ensure the presence of a tumor or the presence of any other medical condition such as testicular torsion, hydrocele which collects fluid in the scrotum that resolves on its own without any treatment, and inguinal hernia which is the exit of part of the intestine through a weak area of ​​the groin It often requires surgery, or epididymitis is an infection of the spermatic pathways and is treated with appropriate antibiotics.

 

How is testicular cancer diagnosed?

Testicular cancer is usually diagnosed based on the patient’s symptoms, and the doctor’s physical examination that includes palpating the testicles to look for swelling or masses, and examining the abdomen and lymph nodes to look for signs of cancer spreading.

Doctors resort to a number of auxiliary laboratory and radiological examinations, such as:

Neoplastic markers, in which the level of alpha-fetoprotein (AFP) or HCG in the blood may be elevated, and both may be elevated. These analyzes can be repeated repeatedly during treatment, as they give a picture of the results of the treatment and the extent of improvement or relapse, if it occurs.
Ultrasound imaging to obtain images of the testicles and the tissues around them.
Computed tomography (CT) scan to help determine the stage of the cancer by showing whether it has spread to organs such as the liver and lungs.
A kidney biopsy is a test that can confirm the presence of cancer and the type of cancer cells.

How is testicular cancer treated?

Testicular cancer is treated with a combination of surgery, chemotherapy, radiation, and hormonal therapy, depending on the patient’s condition, the type of tumor and the degree of its spread. Where one or both testicles can be surgically removed, while the remaining treatments are given to eliminate cancerous cells that have moved to other parts of the body. In many cases, treatment leads to a decrease in male fertility, and may cause complete infertility, so the patient is advised to store sperm before starting treatment.

 

the reviewer:

The prostate gland is part of the male reproductive system that produces a fluid that forms an essential part of semen. The prostate is located below the bladder and in front of the rectum and surrounds the urethra (the tube that carries urine from the bladder). Cancer may occur at the expense of prostate cells called prostate cancer, which is next to lung cancer in the order of causes of cancer death in men.What is prostate cancer?

 

Prostate cancer forms when cells of the prostate gland grow abnormally and multiply (due to defects in DNA) and form a mass of cells called a tumor that may grow and invade nearby tissues. This tumor is made up of malignant cells that can spread to other areas of the body. Prostate is a serious disease that affects thousands of men every year, and most cases occur in men older than 65 years.

Prostate cancer is classified globally according to its speed of growth, and it can be fast growing (aggressive) or slow growing (non-aggressive). Fast-growing prostate cancer may grow very quickly and spread to other areas of the body, such as the bones. Non-aggressive prostate cancer does not grow or grow very little over time.

What are the causes of prostate cancer?

The main cause of prostate cancer is not precisely known, but there are many factors that increase the risk of cancer, such as age, obesity, and smoking. The risk of prostate cancer is doubled in smokers compared to non-smokers.

Genes seem to be related to prostate cancer, as the risk of developing it increases if there are infections in the family, and when there is a family history of breast cancer, the risk of prostate cancer may be higher.

What are the symptoms of prostate cancer?

In the early stages of cancer, the patient may not have any symptoms. The symptoms of prostate cancer are related to the size of the prostate and include: frequent urination during the day or night because the prostate surrounds the urethra and can press on it in this case, difficulty starting to urinate and difficulty urinating when standing, which requires sitting while urinating Pain with urination or ejaculation, and blood in the urine or semen.

These early symptoms of prostate cancer may be attributed to several benign (non-cancerous) conditions of the prostate including benign prostatic hypertrophy, prostatitis, and urinary tract infection.

But advanced (late) prostate cancer that has spread from the prostate gland to another part of the body (forming metastases) leads to many important symptoms that indicate the presence of cancer in the body such as unexplained weight loss, fatigue, shortness of breath when doing non-tiring activities Previously, gradually mild and then severe pain in the bone, especially pain in the lower back.

Early diagnosis is the key to successful treatment, and this applies to all types of cancer, so men are recommended to start prostate exams after the age of 50.

How is prostate cancer diagnosed?

Diagnosis is mainly based on symptoms and clinical examination. The clinical examination includes examination of the external genitalia and anal palpation. The doctor often finds a hard, irregular, painless nodule in the prostate, and sometimes the whole prostate is hard and asymmetrical, but the examination may be normal, so it is important to have a laboratory test to check for PSA. The doctor usually orders a series of helpful tests, including:

PSA, a prostatic antigen found in the blood. This analysis rises in all prostate diseases such as prostatitis, benign prostatic hypertrophy and prostate cancer, so its high indicates the presence of a problem, but it does not diagnose it.
Prostate biopsy is the most important way to confirm the diagnosis, where a sample of prostate tissue is taken and then sent for histological examination to confirm or deny infection. The biopsy is usually taken with ultrasound guidance through the rectum.
After prostate cancer is diagnosed, metastases are searched for by radiographs, where ultrasound can assess spread to the neighborhood (bladder, urethra), while distant metastases are searched for by computed tomography (CT scan) or magnetic resonance (MRI).
How is prostate cancer treated?

Some forms of prostate cancer develop very slowly and do not need treatment at all, while others grow very quickly and threaten the patient’s life, so treatment is considered an absolute necessity, and the doctor develops an appropriate treatment plan based on the age, health condition, stage and grade of the cancer.

An aggressive form of prostate cancer can be treated with one of the following options: surgery in which the prostate is radically removed, hormonal therapy such as the use of steroidal anti-androgens such as cyproterone acetate, or radiation therapy.

How can prostate cancer be prevented?

The risk of prostate cancer can be reduced by choosing a diet that includes fruits and vegetables, avoiding foods high in fat, exercising most days of the week and avoiding smoking.

You must remember that early diagnosis is essential, as cancer in its early stages can be cured and eliminated, while it is difficult in advanced cases. Therefore, doctors recommend annual prostate examination and PSA analysis after the age of 50, and may be recommended earlier if there is a family history of prostate cancer.

 

the reviewer:

our centers

ALRAJAA radiology center:

 

This center was renewed on 2013 by adding many of top of the line machines like MRI 1.5T and ultrafast CT scan for coronary imaging.

Articles of Diseases

Working hours:

8 am to 11 pm

Branch manager:

Mr. Ahmad Elayan

Center service include:

X-RAY

CONE BEAM CT (CBCT)

CT scan

Coronary imaging

Ultrasound

MRI

Panoramic x-ray

Mammography

Jabal Amman – Fourth Circle – Abu Firas Al Hamdani Street – Jewel of the Kingdom Complex:

 

• X-RAY
• Ultrasound imaging
Cone beam 3D dental imaging
• MRI *
Computed Tomography *CT Scan
• DEXA osteoporosis imaging device

Articles of Diseases 

Albasma radiology center:

 

The largest radiology center in region and was opened on 2017 and its area around 1000m2 .
The center includes the administrative offices, radiologist reporting offices, and many radiology rooms with different radiology devices provided from siemens Germany .
Working hours:
8 am to 9 pm
Branch manager:
Mrs. Amal Salameh
Center service include:
x-ray
PET SACN
Cone beam CT (CBCT)
CT scan
Fluoroscopy
GAMMA CAMERA
ULTRASOUND
MRI
Coronary CT scan
Mammography
Hysterosalpingogram
DEXA scan
FIBROSCAN
PANORMIC X-RAY

Jordan radiology center :

This center was opened on late 2019 in front of Jordan hospital at al safa complex 3

This center was provided with the latest open MRI machine and other new machines

Working hours:

8 am to 9 pm

Branch manager

Muhannad Abdelrahman

Maggie MRI radiology center :

 

The first branch of MEDRAY opened on 15/8/2009

And it was the first outside hospital center provide MRI imaging in Jordan

The center renewed on 2022 by removing the old MRI and adding a brand new MRI machine by Philips Germany

Working hours:

8 am to 9 pm

Branch manager:

Muhannad Abdelrahman

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