Ewing's sarcoma overview: Difference between revisions

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==Overview==
==Overview==
'''Ewing's sarcoma''' is the common name for ''[[primitive neuroectodermal tumor]]''. It is a rare disease, and until recently, it had a very low long term survival rate.  It is a small round-cell [[tumor]] in which [[cancer]] cells are found in the [[bone]] or in soft [[biological tissue|tissue]] (rarer). 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 male teenagers.
'''Ewing's sarcoma''' is the common name for ''[[primitive neuroectodermal tumor]]''. It is a rare disease, and until recently, it had a very low long term survival rate.  It is a small round-cell [[tumor]] in which [[cancer]] cells are found in the [[bone]] or in soft [[biological tissue|tissue]] (rarer). 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 male teenagers.
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.


==References==
==References==

Revision as of 14:43, 15 December 2011

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Assistant Editor(s)-In-Chief: Michael Maddaleni, B.S.

Overview

Ewing's sarcoma is the common name for primitive neuroectodermal tumor. It is a rare disease, and until recently, it had a very low long term survival rate. It is a small round-cell tumor in which cancer cells are found in the bone or in soft tissue (rarer). 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 male teenagers.

References

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