Inclusion body myositis long after dermatomyositis: A report of two cases

被引：0

作者：

McCoy, AL ^{[1
]}

Bubb, MR ^{[1
]}

Plotz, PH ^{[1
]}

Davis, JC ^{[1
]}

机构：

[1] NIAMSD, Arthrit & Rheumatism Branch, NIH, Bethesda, MD 20892 USA

来源：

CLINICAL AND EXPERIMENTAL RHEUMATOLOGY | 1999年 / 17卷 / 02期

关键词：

dermatomyositis; polymyositis; inclusion body myositis; inflammatory; myopathy; autoimmunity;

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Dermatomyositis, polymyositis, and inclusion body myositis are rare illnesses which appear to be distinct in clinical and pathologic features, pathogenesis, natural history, and response to therapy. We report two patients who first developed dermatomyositis, and then, after a disease-free interval of many years, developed inclusion body myositis. This may have useful therapeutic implications for patients with dermatomyositis whose illness bocomes refractory to treatment.

引用

页码：235 / 239

页数：5

共 33 条

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