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[肺泡软组织肉瘤]

[Alveolar soft tissue sarcoma].

作者信息

Poroshin K K, Krylov L M, Kudriavtsev B N

出版信息

Arkh Patol. 1989;51(5):51-8.

PMID:2774995
Abstract

Clinical and morphological manifestations of alveolar soft tissue sarcoma (ASTS) are presented on the basis of 19 examinations performed by the authors and data available in the literature. ASTS has been found to be more common in young women and to be usually located in the thick layers of the proximal parts of the extremities. The tumor generally shows slow growth and late occurrence of metastases. It has been demonstrated that ASTS has an organoid structure, namely alveolar grouping of cells, abundance of capillaries, and its cells contain PAS-positive inclusions. In atypical ASTS, the prognosis has been found to be less favourable. The crystalloid inclusions that are absent in other soft tissue neoplasms are a characteristic ultrastructural sign of ASTS. The genesis of ASTS remains controversial but it cannot be ruled out that it is related to the elements of the APUD-system.

摘要

基于作者进行的19例检查及文献中的可用数据,介绍了肺泡软组织肉瘤(ASTS)的临床和形态学表现。已发现ASTS在年轻女性中更为常见,且通常位于四肢近端的厚层部位。该肿瘤一般生长缓慢,转移发生较晚。已证实ASTS具有类器官结构,即细胞呈肺泡状排列、有丰富的毛细血管,且其细胞含有PAS阳性包涵体。在非典型ASTS中,预后较差。其他软组织肿瘤中不存在的晶体包涵体是ASTS的特征性超微结构标志。ASTS的起源仍存在争议,但不能排除它与APUD系统的成分有关。

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