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Ewing's Sarcoma
Alternate Names : Ewing's Family of Tumors, Primitive Neuroectodermal Tumors (PNET)
DefinitionEwing's sarcoma is a malignant (cancerous) bone tumor which affects children.
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Overview, Causes, & Risk Factors
Ewing 's sarcoma can occur any time during childhood, but usually develops during puberty, when bones are growing rapidly. It is uncommon in African-American, African, and Chinese children.
The tumor may arise anywhere in the body, usually in the long bones of the arms and legs, the pelvis, or the chest. It may also develop in the skull or the flat bones of the trunk.
There are few symptoms. The most common is pain and occasionally swelling at the site of the tumor. Children may also break a bone at the site of the tumor after a seemingly minor trauma (pathologic fracture). Fever may also be present.
The tumor often spreads (metastasis) to the lungs and other bones. Metastasis is present in approximately one-third of children with this condition at the time of diagnosis.
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Definition Ewing's Sarcoma Overview, Causes, & Risk Factors Ewing's Sarcoma Symptoms & Signs Ewing's Sarcoma Diagnosis & Tests Ewing's Sarcoma Treatment Ewing's Sarcoma Prognosis Ewing's Sarcoma Complications Ewing's Sarcoma Support Groups Calling Your Health Care Provider
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Bone Tumors Cancer Tumor
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Cancer - Resources Chemotherapy Fever Flat Bones Long Bones Metastasis Radiation Therapy Resources Stress and Anxiety Surgical Excision Swelling
Review Date : 7/17/2002
Reviewed By : Scott Howard, M.D., M.S., Department of Pediatric Hematology/Oncology, St. Jude Children's Research Hospital, Memphis, TN. Review provided by VeriMed Healthcare Network.
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