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Idiopathic inflammatory myopathies

被引：61
作者：
Amato, AA
Barohn, RJ
机构：
[1] UNIV TEXAS, HLTH SCI CTR, DEPT MED, NEUROMUSCULAR SERV, SAN ANTONIO, TX 78284 USA
[2] UNIV TEXAS, SW MED CTR, DEPT NEUROL, DALLAS, TX 75235 USA
来源：
NEUROLOGIC CLINICS | 1997年 / 15卷 / 03期
关键词：
D O I：
10.1016/S0733-8619(05)70337-6
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
Dermatomyositis, polymyositis, and inclusion body myositis are the major categories of idiopathic inflammatory myopathy. These inflammatory myopathies are distinct clinically, histologically, and pathogenically. Features of dermatomyositis and polymyositis can overlap with those of other autoimmune connective tissue diseases. Ln this article, the authors review the characteristic features of these myopathies, update the recent developments in this area, and provide a framework for treatment.
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页码：615 / +
页数：1
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