Ewing's sarcoma
Ewing's sarcoma is the common name for primitive neuroectodermal tumor. It is a rare disease in which cancer cells are found in the bone or in soft tissue. The most common areas in which it occurs are the pelvis, the femur, the humerus, and the ribs. James Ewing (1866-1943) first described the tumor, establishing that the disease was separate from lymphoma and other types of cancer known at that time. Ewing's sarcoma occurs most frequently in teenagers.
Related Topics:
Tumor - Cancer - Bone - Tissue - Pelvis - Femur - Humerus - Ribs - James Ewing - 1866 - 1943 - Lymphoma - Teenagers
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Ewing's sarcoma is the result of a translocation between chromosomes 11 and 22, which fuses the EWS gene of chromosome 22 to the FLI1 gene of chromosome 11.
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~ Table of Content ~
| ► | Introduction |
| ► | Clinical Findings |
| ► | Imaging Findings |
| ► | Differential Diagnosis |
| ► | Treatment |
| ► | Prognosis |
| ► | Useful Links |
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