[儿童滑膜肉瘤的形态学变异性]

[Morphological variability of synovial sarcoma in childhood].

作者信息

Taege C, Holzhausen H-J, Harms D, Katenkamp D, Guenther G, Hauptmann S

机构信息

Institut für Pathologie der Martin-Luther-Universität Halle-Wittenberg.

出版信息

Pathologe. 2005 Mar;26(2):159-62. doi: 10.1007/s00292-004-0746-x.

DOI:10.1007/s00292-004-0746-x

PMID:15690158

Abstract

We report on an unusual locally recurrent plantar soft tissue sarcoma in a 7-years-old boy. Due to an unusual morphology a clear diagnosis was initially not possible. The histologically different recurrent tumor was classified as synovial sarcoma by means of immunohistochemistry, ultrastructural and molecular analysis. This case demonstrates the variable morphological appearance of synovial sarcoma and the value of modern diagnostic procedures in such circumstances.

摘要

我们报告了一例7岁男孩罕见的足底软组织肉瘤局部复发病例。由于形态异常，最初无法明确诊断。通过免疫组织化学、超微结构和分子分析，将组织学上不同的复发肿瘤归类为滑膜肉瘤。该病例展示了滑膜肉瘤形态学表现的多样性以及现代诊断方法在此类情况下的价值。