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特发性巨细胞性心肌炎——一例病例报告及文献复习

Idiopathic giant cell myocarditis--a case report and review of literature.

作者信息

Konapur P G, Dhaded A V, Udayakumar M

机构信息

Department of Pathology, Al Ameen Medical College, Bijapur, Karnataka.

出版信息

Indian J Pathol Microbiol. 2003 Apr;46(2):241-3.

Abstract

Idiopathic giant cell myocarditis (IGCM) is a rare clinicopathological entity which is usually known to cause in more than half the cases sudden death. The histological features are characteristic with a central area of myocardial necrosis and a rich cellular infiltration of lymphocytes with a few eosinophils, plasma cells, macrophages and multinucleated giant cells. We hereby report a case of IGCM in a 72 year old male with history of sudden death. This case is being presented for its rarity and a review of literature is made.

摘要

特发性巨细胞心肌炎(IGCM)是一种罕见的临床病理实体,通常已知在超过半数的病例中会导致猝死。其组织学特征具有特异性,表现为心肌坏死的中央区域以及淋巴细胞、少量嗜酸性粒细胞、浆细胞、巨噬细胞和多核巨细胞的丰富细胞浸润。我们在此报告一例72岁男性特发性巨细胞心肌炎病例,该患者有猝死病史。此病例因其罕见性而被呈现,并对相关文献进行了回顾。

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