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侵袭性组织细胞增多症X的眼部受累情况。

Ophthalmic involvement in aggressive histiocytosis X.

作者信息

MacCumber M W, Hoffman P N, Wand G S, Epstein J I, Beschorner W E, Green W R

机构信息

Wilmer Ophthalmological Institute, Johns Hopkins University School of Medicine, Baltimore, MD.

出版信息

Ophthalmology. 1990 Jan;97(1):22-7.

PMID:2179796
Abstract

The authors report the clinicopathologic features of an unusually aggressive form of histiocytosis X (Langerhans' cell histiocytosis) in a 36-year-old man who presented with diplopia and early development of pituitary failure from presumed involvement of the hypothalamus. Results of postmortem examination showed infiltrates of histiocytes and mixed inflammatory cells, with a variably dense desmoplastic tissue within the orbit and sclera bilaterally, the left optic nerve, choroid, emissary canals, and many other body systems including the pituitary, heart, lung, and gastrointestinal tract. Diagnosis was confirmed by immunohistochemical staining of large histiocytes within diseased areas, with anti-T6 and anti-S-100 antibodies.

摘要

作者报告了一名36岁男性中一种异常侵袭性组织细胞增多症X(朗格汉斯细胞组织细胞增多症)的临床病理特征,该患者表现为复视,且因下丘脑可能受累而早期出现垂体功能衰竭。尸检结果显示组织细胞和混合性炎性细胞浸润,双侧眼眶和巩膜、左侧视神经、脉络膜、导血管以及包括垂体、心脏、肺和胃肠道在内的许多其他身体系统内有不同程度致密的促纤维组织增生。通过用抗T6和抗S-100抗体对病变区域内的大组织细胞进行免疫组化染色,确诊了该病。

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