There are many different types of treatment for Childhood Rhabdomyosarcomosis, and some methods may be better suited for children than others. The first step is to find out if your child has this rare cancer, and how to recognize the signs and symptoms. Treatment options will depend on the stage of the disease and the location of the tumor. If your child has multiple symptoms, such as pain or difficulty breathing, you should seek medical attention.
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There are several different symptoms of Childhood Rhabdomyosarcomosis, depending on where it has spread. In the first stage, a tumor is considered a favorable site and has a higher chance of cure. In stage 2, a tumor is smaller than five centimeters in size and is usually not spread to other parts of the body. In stage 4, a tumor may be any size and have spread to distant areas or lymph nodes.
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If treatment options are successful, 70 percent of children with Childhood Rhabdomyosarcomosis survive five years after diagnosis. If treated in the early stages, patients enjoy a cure rate of 80 percent or more. Current research focuses on identifying better combinations of drugs and treatments to improve the patient's prognosis. However, if you suspect your child has this cancer, it is vital that you seek medical attention.
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A full medical workup is important for determining rhabdomyosarcoma symptoms. To make a diagnosis, your doctor may conduct a needle biopsy or a surgical cut. This procedure will remove a small sample of tumor tissue and will reveal if it's cancer or not. In addition, your doctor may perform an MRI or CT scan to find whether the cancer has spread.
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Treatment for Childhood Rhabdomyosarcomosis involves surgery, radiation therapy, and chemotherapy. The order of these treatments depends on the size of the tumor and the extent of its spread. If surgery is not possible, you may have to undergo palliative care to help alleviate symptoms. Nutritional supplements, therapy, and relaxation techniques are some of the methods that may be helpful. The last step is to discuss your treatment options with your child's physician.
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Childhood Rhabdomyosarcomosa is a rare form of cancer that affects the muscle tissue. It starts in mesenchymal cells that transform into muscle and tumors. The disease is rarely fatal, and only around 500 people are diagnosed in the United States each year. Rhabdomyosarcoma most commonly affects the head and neck, the arms, and the legs. It can even affect the genitourinary system, including the bladder.
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Children can develop Rhabdomyosarcoma in any part of their bodies, and symptoms include muscle pain, urination, and inability to urinate. Childhood Rhabdomyosarcoma can be diagnosed as early as two years old. Children between the ages of 2 and six are the most likely to develop Childhood Rhabdomyosarcoma. However, it is rarer in boys and more common in whites than in black girls.
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Other symptoms of RMS include a chronic cough, enlarged lymph nodes, and bone pain. Children may also experience bleeding or difficulty urinating. Their symptoms may vary, depending on where the cancer has spread. A child with these symptoms should be evaluated by a doctor to be sure it is the cancer. They should also be evaluated for any other conditions that may be causing the symptoms. If the symptoms persist or worsen, it is time to see a doctor.
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As with all cancers, symptoms of Childhood Rhabdomyosarcomosa may not be obvious at first. However, if they are present, they may be a sign of the disease. While symptoms will vary according to the primary site of the tumor, they are common and should not be ignored. Symptoms may also be present even if the tumor is in an area other than the skin.
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