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淋巴瘤样肉芽肿病患者的中枢神经系统免疫母细胞肉瘤。

Immunoblastic sarcoma of the central nervous system in a patient with lymphomatoid granulomatosis.

作者信息

Reddick R L, Fauci A S, Valsamis M P, Mann R B

出版信息

Cancer. 1978 Aug;42(2):652-9. doi: 10.1002/1097-0142(197808)42:2<652::aid-cncr2820420236>3.0.co;2-c.

Abstract

A 26-year-old man with lymphomatoid granulomatosis (LYG) was found at postmortem examination to have an immunoblastic sarcoma involving the central nervous system. Residual evidence of LYG was present only in the lungs at autopsy. Studies for intracellular immunoglobulin utilizing the immunoperoxidase technique showed a marked polyclonal reaction in sections of lymph nodes and occasional cells in the cellular central nervous system tumor that stained for intracellular immunoglobulins (IgG, IgM and both kappa and lambda). This case may represent another example of immunoblastic sarcoma occurring in the presence of an abnormal immune state or proliferation.

摘要

一名患有淋巴瘤样肉芽肿病(LYG)的26岁男性在尸检时被发现患有累及中枢神经系统的免疫母细胞肉瘤。尸检时,LYG的残留证据仅存在于肺部。利用免疫过氧化物酶技术对细胞内免疫球蛋白进行的研究显示,在淋巴结切片以及细胞性中枢神经系统肿瘤中偶尔出现的细胞中,存在明显的多克隆反应,这些细胞可被细胞内免疫球蛋白(IgG、IgM以及κ和λ)染色。该病例可能代表了在异常免疫状态或增殖情况下发生的免疫母细胞肉瘤的另一个例子。

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