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伴有束状毛细血管及少量细胞浸润的坏死性肌病:1例与皮肌炎皮肤表现相关的病例

Necrotizing myopathy with pipestem capillaries and minimal cellular infiltration: a case associated with cutaneous signs of dermatomyositis.

作者信息

Authier F J, Kondo H, Ghnassia R T, Revuz J, Gherardi R K

机构信息

Groupe Nerf-Muscle, Hôpital Henri-Mondor, Faculté de Médecine, Créteil, Paris.

出版信息

Neurology. 1996 May;46(5):1448-51. doi: 10.1212/wnl.46.5.1448.

DOI:10.1212/wnl.46.5.1448
PMID:8628498
Abstract

In 1991, Emslie-Smith and Engel described a distinct form of idiopathic inflammatory myopathy they called "necrotizing myopathy with pipestem capillaries, microvascular deposition of the complement membrane attack complex (MAC) and minimal cellular infiltration." We describe a patient with exercise-dependent painful myopathy related to a necrotizing myopathy with pipestem capillaries in whom mild cutaneous signs of dermatomyositis were detected 7 years after onset and who subsequently developed multiple cerebral infarcts.

摘要

1991年,埃姆斯利 - 史密斯和恩格尔描述了一种独特形式的特发性炎性肌病,他们称之为“伴有束状毛细血管、补体膜攻击复合物(MAC)微血管沉积及最小限度细胞浸润的坏死性肌病”。我们描述了一名患有与伴有束状毛细血管的坏死性肌病相关的运动依赖性疼痛性肌病的患者,该患者在发病7年后检测到皮肌炎的轻度皮肤体征,随后发生了多发性脑梗死。

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Necrotizing myopathy with pipestem capillaries and minimal cellular infiltration: a case associated with cutaneous signs of dermatomyositis.伴有束状毛细血管及少量细胞浸润的坏死性肌病:1例与皮肌炎皮肤表现相关的病例
Neurology. 1996 May;46(5):1448-51. doi: 10.1212/wnl.46.5.1448.
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