模仿肢带型肌营养不良的儿童期起病的包涵体肌炎
Childhood onset inclusion body myositis mimicking limb-girdle muscular dystrophy.
作者信息
Riggs J E, Schochet S S, Gutmann L, Lerfald S C
机构信息
Department of Neurology, West Virginia University School of Medicine, Morgantown 26506.
出版信息
J Child Neurol. 1989 Oct;4(4):283-5. doi: 10.1177/088307388900400406.
PMID:2551952
Abstract
Inclusion body myositis was initially recognized in patients with "steroid-resistant polymyositis" and subsequently in patients with other immune-mediated disorders. The finding of inclusion body myositis in a patient diagnosed for 30 years as having limb-girdle muscular dystrophy suggests yet another patient pool that may harbor this entity.
摘要
包涵体肌炎最初在“类固醇抵抗性多发性肌炎”患者中被识别出来，随后在患有其他免疫介导疾病的患者中也被发现。一名被诊断为肢带型肌营养不良30年的患者被发现患有包涵体肌炎，这表明可能还有另一类患者群体存在这种疾病。
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