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[良性演进性网状组织细胞增多症(桥本-普利茨克型)。电子显微镜研究]

[Reticulohistiocytosis of benign evolution (Hashimoto-Pritzker type). Electron microscopy study].

作者信息

Laugier P, Hunziker N, Laut J, Orusco M, Osmos L

出版信息

Ann Dermatol Syphiligr (Paris). 1975;102(1):21-31.

PMID:179459
Abstract

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.

摘要

我们描述了一种罕见的组织细胞增多症,其特征为出生时即出现大量皮肤肿瘤性病变,在2个月内自发消退,无内脏病变及全身症状。光镜检查显示组织细胞,其中一些含有不规则核,胞质呈泡沫状,周围有许多红细胞。电镜检查显示组织细胞胞质中有髓鞘样包涵体和“蠕虫状”小体。我们认为,桥本和普利茨克首次且仅一次描述了一种类似的解剖临床实体。

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