包涵体肌炎：1例合并胶原血管病且治疗有效的病例。
Inclusion body myositis: a case with associated collagen vascular disease responding to treatment.
作者信息
Lane R J, Fulthorpe J J, Hudgson P
出版信息
J Neurol Neurosurg Psychiatry. 1985 Mar;48(3):270-3. doi: 10.1136/jnnp.48.3.270.
Abstract
Patients with inclusion body myositis demonstrate characteristic histological and electronmicroscopical abnormalities in muscle and are generally considered refractory to treatment. A patient with inclusion body myositis is described with evidence of associated autoimmune disease, who responded to steroids.
摘要
包涵体肌炎患者的肌肉表现出特征性的组织学和电子显微镜异常，通常被认为对治疗难治。本文描述了一名伴有自身免疫性疾病证据的包涵体肌炎患者，该患者对类固醇治疗有反应。
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