良性演变的网状组织细胞增多症(桥本-普利兹克型)。电子显微镜研究]。

P Laugier, N Hunziker, J Laut, M Orusco, L Osmos
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引用次数: 0

摘要

我们描述了一种罕见的组织细胞增多症,其特征是出生时出现许多皮肤肿瘤病变,并在2个月内自发消失,无内脏病变,无全身症状。光镜下可见组织细胞,其中一些细胞含有不规则的细胞核和被许多红细胞包围的粘液质。电镜显示组织细胞细胞质和“蚓状”体中有髓样包涵体。在我们看来,类似的解剖临床实体是第一次描述,只有一次由桥本和普利兹克。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Reticulohistiocytosis of benign evolution (Hashimoto-Pritzker type). Electron microscopy study].

We describe a rare form of histiocytosis, characterized by numerous tumoral lesions of the skin appearing at birth and desappearing spontaneously within 2 month without visceral lesions and without systemic symptoms. Light microscopy shows histiocytes, some of which contain an irregular nucleus with a spumous cytoplasm surrounded by many red blood cells. Electron microscopy shows myelinoid inclusions in the histiocyte cytoplasm and "vermiform" bodies. In our opinion, a similar anatomoclinical entity was described for the first time and only once by Hashimoto and Pritzker.

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