Inflammatory myopathies and systemic disorders: a review of immunopathogenetic mechanisms and clinical features

被引:0
|
作者
R. Mantegazza
P. Bernasconi
Paolo Confalonieri
Ferdinando Cornelio
机构
[1] Department of Neuromuscular Diseases,
[2] “C. Besta” National Neurological Institute,undefined
[3] Via Celoria 11,undefined
[4] I-20133 Milan,undefined
[5] Italy Tel.: +39-2-2394282,undefined
[6] Fax: +39-2-70633874,undefined
[7] e-mail: mantega@imiucca.csi.unimi.it,undefined
来源
Journal of Neurology | 1997年 / 244卷
关键词
Key words Inflammatory; myopathies; Autoimmunity; Muscle; Collagen vascular diseases; Malignancies;
D O I
暂无
中图分类号
学科分类号
摘要
The inflammatory myopathies are a heterogeneous group of muscle diseases characterized by muscle degeneration mediated by inflammatory processes. They may be idiopathic, as in polymyositis, dermatomyositis and inclusion body myositis, or associated with systemic disorders such as malignancies, overlap syndromes, and retroviral infection. The pathogenesis of each disease is discussed together with more recent molecular and cellular immunology findings. Salient diagnostic, clinical and pharmacological features are also reviewed.
引用
收藏
页码:277 / 287
页数:10
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