海蓝组织细胞综合征。文献综述[1例成人特发性脾肿大]。

M C Vacher-Lavenu, V Baron-Selme, R Abelanet, A Boissonnas, C Laroche
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引用次数: 0

摘要

本文报道一例特发性脾肿大合并ceroid组织细胞增多症,即所谓的海蓝色组织细胞增多症。描述了染色海蓝巨噬细胞和含cerloid巨噬细胞的组织学、组织化学和超微结构特征,并讨论了它们的生理病理意义。注意到的区别,特发性和继发性或相关的形式,并强调病理诊断的实用价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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[Sea-blue histiocyte syndrome. Review of the literature apropos of a case of idiopathic splenomegaly in the adult].

A case of idiopathic splenomegaly with ceroid histiocytosis--the so-called sea-blue histiocytosis--is reported with reference to the literature. The histological, histochemical and ultrastructural features of stained sea-blue and ceroid-containing macrophages are described and their physiopathological significance is discussed. Attention is drawn to the distinctions, between idiopathic and secondary or associated forms, and the practical value of the pathological diagnosis is emphasized.

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