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类风湿性肌炎。临床及组织学特征与可能的发病机制。

Rheumatoid myositis. Clinical and histologic features and possible pathogenesis.

作者信息

Halla J T, Koopman W J, Fallahi S, Oh S J, Gay R E, Schrohenloher R E

出版信息

Arthritis Rheum. 1984 Jul;27(7):737-43. doi: 10.1002/art.1780270703.

Abstract

Thirty-one patients with rheumatoid arthritis were consecutively studied for evidence of muscle involvement, using muscle biopsy and electromyography. The patients were initially separated into 4 clinical categories: inactive peripheral joint disease (6 patients); active peripheral joint disease (10 patients); systemic disease and a disproportionately elevated sedimentation rate for the degree of mild synovitis (SERD) (11 patients); or elevated creatinine phosphokinase level (4 patients). In addition to routine histology, muscle tissue was examined for de novo synthesis of IgM and IgM rheumatoid factor, and by indirect immunofluorescence for the presence of immunoglobulin and complement deposits. Our results indicate that: muscle fiber necrosis occurs frequently in patients with rheumatoid arthritis; rheumatoid myositis, defined as muscle fiber necrosis and mononuclear cell infiltration, is a distinct entity and occurs particularly in patients with SERD or an elevated creatinine phosphokinase level; and only muscle from patients with rheumatoid myositis exhibited de novo synthesis of rheumatoid factor and significant quantities of IgM, indicating that local immune events may be important in the pathogenesis of this entity.

摘要

对31例类风湿性关节炎患者连续进行研究,采用肌肉活检和肌电图检查以寻找肌肉受累的证据。患者最初被分为4种临床类型:非活动性外周关节疾病(6例);活动性外周关节疾病(10例);全身性疾病且轻度滑膜炎程度下血沉不成比例升高(SERD)(11例);或肌酸磷酸激酶水平升高(4例)。除常规组织学检查外,还对肌肉组织进行了IgM和IgM类风湿因子的从头合成检测,并通过间接免疫荧光检测免疫球蛋白和补体沉积情况。我们的结果表明:类风湿性关节炎患者中肌纤维坏死经常发生;类风湿性肌炎定义为肌纤维坏死和单核细胞浸润,是一种独特的病症,尤其发生在SERD患者或肌酸磷酸激酶水平升高的患者中;并且只有类风湿性肌炎患者的肌肉表现出类风湿因子的从头合成和大量IgM,这表明局部免疫事件在该病症的发病机制中可能很重要。

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