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[海蓝色组织细胞综合征。结合一例成人特发性脾肿大病例对文献的综述]

[Sea-blue histiocyte syndrome. Review of the literature apropos of a case of idiopathic splenomegaly in the adult].

作者信息

Vacher-Lavenu M C, Baron-Selme V, Abelanet R, Boissonnas A, Laroche C

出版信息

Sem Hop. 1984 May 3;60(19):1333-41.

PMID:6326324
Abstract

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.

摘要

报告了一例伴有类蜡质组织细胞增多症(即所谓的海蓝色组织细胞增多症)的特发性脾肿大病例,并参考了相关文献。描述了染色的海蓝色和含类蜡质巨噬细胞的组织学、组织化学和超微结构特征,并讨论了它们的生理病理学意义。文中提请注意特发性与继发性或相关形式之间的区别,并强调了病理诊断的实际价值。

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