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</html>";s:4:"text";s:2844:"Rhabdomyosarcoma Symptoms . Rhabdomyosarcoma Symptoms The symptoms of Rhabdomyosarcoma depends on the location of the tumor. More males than females and more caucasians than African-Americans develop rhabdomyosarcoma. Pain is usually present, this is a body’s defense mechanism to alert an individual that there is something wrong in the area where an individual can feel pain. The 5-year survival rate for teens ages 15 to 19 is 46%. For example, the overall 5-year survival for children with RMS is about 70%, while survival in adults is lower. For pediatric embryonal, alveolar, and anaplastic rhabdomyosarcoma, learn about the disease presentation, diagnosis, prognosis, treatment regimens, and clinical trials in this expert-reviewed summary. About two-thirds of rhabdomyosarcoma cases are diagnosed in children younger than age 10. But other factors can also affect a person’s outlook, such as their age and how well the cancer responds to treatment. Children ages 1 to 9 have a better prognosis than people in other age groups. Rhabdomyosarcoma is the most common type of soft tissue sarcoma in children. The outlook (prognosis) and treatment decisions depend on the type of rhabdomyosarcoma, where it starts, tumor size and whether the cancer has spread. The symptoms that are associated with RMS can vary widely depending on where the tumor develops. However, the rate varies widely depending on the tumor location, stage and risk group, and the child’s age. Survival rates for rhabdomyosarcoma. Children with orbital RMS (about 10% of all cases of RMS), may present with a bulging or swollen eye . For a person with RMS, the risk group is important in estimating their outlook. Major advancements in the treatment of rhabdomyosarcoma have significantly improved outcomes. What are the symptoms of rhabdomyosarcoma? Rhabdomyosarcoma is a rare type of cancer that affects muscle tissue, mostly in children and adolescents. It can occur anywhere in the body, but usually the head and neck, arms and legs, and urinary and reproductive organs. Patients with nonmetastatic rhabdomyosarcoma have an overall survival rate of about 71% with combined modality therapy (chemotherapy, radiation therapy, and surgery) [].The prognosis of children with rhabdomyosarcoma is determined by clinical group, stage, histology, and age at presentation. The stage is one of the most important factors in determining a person's prognosis (outlook). This is known as the stage of the cancer. Rhabdomyosarcoma (cancer of striated muscle) in children is treated with chemotherapy, radiation therapy, and surgery. Treatment is usually with a combination of surgery, chemotherapy and radiation therapy. Once rhabdomyosarcoma (RMS) has been diagnosed and the type of RMS identified, doctors need to assess how much cancer there is and where it has spread. ";s:7:"keyword";s:26:"rhabdomyosarcoma prognosis";s:5:"links";s:1176:"<a href="http://sljco.coding.al/haovssy/clarins-bust-beauty-extra-lift-gel-boots">Clarins Bust Beauty Extra-lift Gel Boots</a>,
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