One of the most common types of soft tissue cancer in children is Childhood Rhabdomyosarcomal tumors. It starts in cells that develop into skeletal muscles and can develop anywhere in the body. Childhood Rhabdomyosarcoma symptoms can vary widely and are dependent on the location and size of the tumor. Depending on the stage of the disease, your doctor may use radiation therapy, chemotherapy, or surgery to remove the tumor. Treatment may also include follow-up visits with your doctor.
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Treatment for childhood rhabdomyosarcoma depends on the stage and extent of cancer in the tumor. Surgical procedures are typically performed to remove the tumor, but some patients require chemotherapy. After surgery, a pathologist may use chemotherapy or surgery to kill any remaining cancer cells. Surgery is the main treatment option for childhood rhabdomyosarcoma, and may also include radiation therapy and chemotherapy.
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Childhood Rhabdomyosarcoman treatment depends on the cancer stage. To diagnose childhood rhabdomyosarcoma, your doctor will perform a complete medical exam. A needle biopsy will be used to remove a small sample of the abnormal tissue. This sample will be evaluated in order to make a more accurate diagnosis. Another test used for this purpose is computed tomography (CT), a test that uses X-rays and computer technology to create a detailed picture of the tumor.
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Childhood Rhabdomyosarcomia symptoms may be vague or similar to symptoms of other childhood conditions. The most important thing to remember is that RMS is a medical emergency, and you should never ignore any unusual health problems in your child. Even if the tumor is small, symptoms can be vague and unnoticeable. But if it grows bigger, your child will most likely experience pain.
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Childhood Rhabdomyosarcoman tumors are fast-growing and can develop in a variety of soft tissues. The most common areas are the head and neck, urinary tract, limbs, and genital tract. About 3% of all children get rhabdomyosarcoma. It tends to develop in boys, and less frequently in black girls.
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If your child is diagnosed with Childhood Rhabdomyosarcoman tumors, your doctor will likely recommend surgery or chemotherapy. Surgery will allow doctors to accurately diagnose the type of tumor and determine its stage. If surgery is not possible, chemotherapy may be given to help suppress tumor growth or kill cancer cells in the surrounding tissue. It may also involve chemotherapy to shrink large tumors. You can learn more about the different treatment options for childhood rhabdomyosarcoma by visiting the NCI website.
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In children, Rhabdomyosarcoma may cause a lump to form in the muscle tissue. A lump may be a symptom of childhood Rhabdomyosarcoma, and it will only get larger if left untreated. If you suspect your child of having this cancer, visit your doctor immediately. The early diagnosis will greatly affect your prognosis and treatment options.
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Childhood Rhabdomyosarcomia is a rare type of cancer in children. Approximately five percent of children develop this form of soft tissue sarcoma. This type of cancer often starts in the muscle attached to bones, but it can also occur in other locations. The most common locations for Rhabdomyosarcoma in children are the head and neck, arms, legs, and genital organs.
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Other Childhood Rhabdomyosarcomia symptoms include chronic cough, enlarged lymph nodes, and bone pain. These symptoms may be accompanied by weakness and weight loss. Your doctor will ask you about your child's symptoms to help them diagnose the condition. However, it is important to remember that some of these symptoms may be caused by something less serious. Your doctor will want to know what the exact symptoms are so that you can choose the best treatment for your child.
