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Childhood Rhabdomyosarcoma Symptoms - Oren Zarif - Childhood Rhabdomyosarcoma

If you notice any of these symptoms in your child, they could be signs of Childhood Rhabdomyosarcomoma, a rare cancer that affects young children. Fortunately, the disease is very rare, and with proper care, 70 percent of children with the disease survive five years or longer. This prognosis remains good after five years, but the early diagnosis and aggressive therapy are crucial to the overall survival of the child.

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Childhood Rhabdomyosarcomoma symptoms vary, depending on the location and size of the tumor. The symptoms are similar to those of other childhood diseases, making early detection crucial. A lump that is visible and painless is often the first sign. However, the size of the tumor can alter the symptoms, so they may not be present at all. If a tumor is large and painful, the symptoms may vary.

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The cancer's stage will dictate the course of treatment. Stages vary from stage one to stage four, and determine the best treatment. Stage one is limited to one site, while stage four may involve cancer that has spread to other parts of the body. Treatment will depend on the extent of the cancer's spread, and can include radiation therapy, chemotherapy, and surgery. In severe cases, the cancer may spread to other parts of the body.

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Radiotherapy is another treatment option for childhood Rhabdomyosarcoma. It targets the cancer cells while doing very little damage to healthy tissue. Radiotherapy is usually given after surgery. The side effects of radiotherapy vary, depending on the type of treatment and the area of the body treated. Most of the time, these side effects disappear on their own after treatment has stopped. Some children may experience a few months or years after surgery, depending on their body type.

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A child may exhibit these symptoms if he has high birth weight. These risk factors increase the likelihood of childhood rhabdomyosarcoma. In addition to the aforementioned risk factors, a child's gender may increase the risk. Regardless of the type of childhood rhabdomyosarcoma, genetic conditions can increase the risk of the disease. As a result, it is important to consult a physician if you notice any of these signs.

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Treatment for childhood rhabdomyosarcoma may include surgery, chemotherapy, or a combination of the three. The type of treatment depends on the location of the tumor and its size. Surgery is often performed to remove the tumor, although the surgeon will have to carefully plan the surgery so that it does not alter the body's tissues. Chemotherapy is usually given through the vein.

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To confirm a diagnosis, a complete medical workup is performed. A biopsy, a needle-like procedure in which a small amount of abnormal tissue is removed, will help confirm the diagnosis. Another test used to diagnose rhabdomyosarcoma is a computed tomography scan, which combines computer technology with X-rays to determine the extent of the disease.

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Treatment for Childhood Rhabdomyosarcomoma depends on the location of the tumor. It usually begins in the head and neck, and can spread to other parts of the body. Fortunately, there are no known preventative factors for the disease, but genetic testing can help identify family members at risk. Treatment usually involves surgery, chemotherapy, or radiation therapy. Surgery, which removes the tumor, may involve using high-energy rays from a specialized machine.

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After diagnosis, rhabdomyosarcoma treatment usually includes surgery, radiation therapy, or chemotherapy. The order of treatment is dependent on the location of the tumor, the extent of the disease, and the type of childhood Rhabdomyosarcoma. Some treatments may be combined or performed simultaneously. While surgery may be the first treatment for childhood Rhabdomyosarcoma, radiation therapy may be used to control the growth of abnormal cells.

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A growing mass or swelling is the most common childhood Rhabdomyosarcoma symptom. Other symptoms of RMS depend on the location of the tumor. If it occurs in the urinary or reproductive organs, children may experience blood in their urine or difficulty urinating. A tumor in the base of the skull can affect vision, and facial asymmetry and pain are common. If the cancer has spread, imaging studies may be necessary to determine where the tumor is located.

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After diagnosis, some tests may be done after the cancer has been treated. These tests can help determine whether your child's condition has improved or if the cancer has returned. The doctor may also want to see how long these symptoms have lasted. Those symptoms are also signs of cancer. However, these tests are not used to determine the exact cause of the disease. Symptoms may be mild, or they may be accompanied by other symptoms.


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