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Cancers which occur in the connective tissue of the body, such as muscle, fat, and fibrous tissue are usually considered sarcomas. The most common sarcomas in children are rhabdomyosarcoma (muscle), osteosarcoma (bone cells), and Ewing sarcoma (in or outside of bone). However, there are more than 50 other types of other soft tissue sarcomas in children diagnosed about 900 each year:
Symptoms of soft tissue sarcomas vary based on their location. For example, tumors in the arm or leg can cause a lump, swelling around a joint, or pain. Because sarcomas are so rare, it is important that patients receive treatment at medical centers that specialize in children’s and adolescent cancers. This will help to ensure a biopsy is taken which will not affect treatment while providing the necessary tissue to confirm the diagnosis.
The most common risk factors for soft tissue sarcoma are in children with neurofibromatosis or from a family with Li-Fraumeni syndrome. Children with these conditions are more at risk for rhabdomyosarcoma, but account for only a small fraction of cases. These syndromes usually require medical care, so you would know if your child had one of them.
About soft tissue sarcomaIn treatment for soft tissue sarcomaAfter treatment for soft tissue sarcoma