原发性皮肤组织细胞肉瘤。发病率,特征,病程]。

D Canioni, L Barelli, C Butori, J Kermarec
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引用次数: 0

摘要

本文报告1例真正的皮肤组织细胞肉瘤(或克罗斯蒂氏网状病),并为讨论目前用于定义淋巴瘤组织细胞起源的技术、评估组织细胞浸润恶性程度的标准以及组织细胞肉瘤的临床资料和病程提供了基础。特别强调了克罗斯蒂网状病的特点,作者认为这是一种组织细胞肉瘤,通常有良好的结果。他们还试图分离评估疾病预后的病理标准,这似乎因病例而异。撇开未通过超微结构和酶免疫技术研究的病例,作者在皮肤病学文献中只发现了22例原发性皮肤组织细胞肉瘤,包括他们自己的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Primary cutaneous histiocytosarcoma. Incidence, characterization, course].

A case of true cutaneous histiocytosarcoma --or Crosti's reticulosis--is reported, and provides the basis for a discussion of the techniques at present used in defining the histiocytic origin of lymphomas, criteria for assessing the malignancy of histiocytic infiltrates, and clinical data and course of histiocytic sarcomas. Particular emphasis is laid on the characteristics of Crosti's reticulosis, which the authors consider to be a form of histiocytic sarcoma, usually with a favorable outcome. They also attempt to isolate pathological criteria for assessing the prognosis of the disease, which appears to vary substantially from case to case. Setting aside cases which had not been studied by both ultrastructural and enzymo-immunological techniques, the authors found only the twenty-two cases of primary cutaneous histiocytosarcoma in dermatological literature, including their own.

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