Epithelioid sarcoma overview: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{Epithelioid sarcoma}} | {{Epithelioid sarcoma}} | ||
{{CMG}}; {{AE}} {{JH}} | {{CMG}}; {{AE}} {{JH}}; {{Ammu}} | ||
==Overview== | ==Overview== | ||
Revision as of 16:32, 18 February 2016
|
Epithelioid sarcoma Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Epithelioid sarcoma overview On the Web |
|
American Roentgen Ray Society Images of Epithelioid sarcoma overview |
|
Risk calculators and risk factors for Epithelioid sarcoma overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Jesus Rosario Hernandez, M.D. [2]; Ammu Susheela, M.D. [3]
Overview
Epithelioid sarcoma is a rare mesenchymal soft tissue tumor with an epithelioid pattern. It often occurs in the extremities of young people.
Diagnosis is often delayed because of the unusual nature of the tumor.