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白血病性网状内皮细胞增生症与组织细胞淋巴瘤并存:一例报告

Coexistence of leukemic reticuloendotheliosis and histiocytic lymphoma: a case report.

作者信息

Adler S S, Shetty J, Golomb H M

出版信息

Cancer. 1979 May;43(5):1872-80. doi: 10.1002/1097-0142(197905)43:5<1872::aid-cncr2820430542>3.0.co;2-d.

Abstract

A 65-year-old woman had pancytopenia, splenomegaly, and an inaspirable bone marrow. Diagnostic evaluation demonstrated that she had both leukemic reticuloendotheliosis (LRE), or hairy cell leukemia, and an additional lympho-reticular neoplasm, most likely a "histiocytic" lymphoma. The diagnosis of LRE was based on the histopathology of spleen tissue and of a bone marrow biopsy specimen. The diagnosis of diffuse "histiocytic" lymphoma was based on the histopathology of a splenic hilar and a mesenteric lymph node, tumor nodules in the kidney and spleen, and tissue from a mass obstructing a ureter. This is the first well-documented association of a second lympho-reticular neoplasm with LRE. Even relatively gently treatment of the "histiocytic" lymphoma resulted in fatal pancytopenia, illustrating the restricitons on therapy imposed by the marrow impairment due to the LRE.

摘要

一名65岁女性出现全血细胞减少、脾肿大,且骨髓穿刺未能成功取材。诊断评估显示她患有白血病性网状内皮增生症(LRE),即毛细胞白血病,以及另一种淋巴网状肿瘤,很可能是“组织细胞性”淋巴瘤。LRE的诊断基于脾组织和骨髓活检标本的组织病理学检查。弥漫性“组织细胞性”淋巴瘤的诊断基于脾门和肠系膜淋巴结的组织病理学检查、肾和脾内的肿瘤结节以及阻塞输尿管的肿块组织。这是首次有充分记录的第二种淋巴网状肿瘤与LRE相关联的病例。即使对“组织细胞性”淋巴瘤进行相对温和的治疗也导致了致命的全血细胞减少,这说明了LRE导致的骨髓损害对治疗造成的限制。

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