Abstract
The analysis of data from literature and of the author's own 3 observations suggests that epithelioid sarcoma of Enzinger should be separated from soft tissue tumors of obscure genesis. It has a peculiar morphological structure, affects predominantly distal parts of the extremities in the area of tendons and joint capsules, and has some features of the clinical course and prognosis.
摘要
对文献数据及作者自身的3例观察结果分析表明，恩津格上皮样肉瘤应与起源不明的软组织肿瘤区分开来。它具有独特的形态结构，主要累及四肢远端肌腱和关节囊区域，且具有一些临床病程及预后特征。
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