Kraus A, Cifuentes M, Villa A R, Jakez J, Reyes E, Alarcón-Segovia D
Department of Immunology & Rheumatology, Instituto Nacional de la Nutrición Salvador Zubirán, Mexico City, Mexico.
J Rheumatol. 1994 Apr;21(4):649-53.
To describe the findings and course of myositis in primary Sjögren's syndrome (SS).
We studied myositis in SS when clinically indicated. Of 104 patients with SS, we identified 3 cases. In all, the diagnosis was made according to clinical data, biochemical, electromyographic and biopsy criteria. Other autoimmune diseases were excluded.
We found a prevalence of 3% of myositis secondary to SS. There were no significant associations between myositis and other clinical or laboratory variables.
Although rare, myositis must be considered a part of the spectrum of SS. In our experience, treatment with steroids and immunosuppressive drugs was successful.
描述原发性干燥综合征(SS)中肌炎的表现及病程。
在临床有指征时,我们对SS患者中的肌炎进行了研究。在104例SS患者中,我们识别出3例。总体而言,诊断依据临床资料、生化、肌电图及活检标准做出。排除了其他自身免疫性疾病。
我们发现SS继发肌炎的患病率为3%。肌炎与其他临床或实验室变量之间无显著关联。
尽管罕见,但肌炎必须被视为SS疾病谱的一部分。根据我们的经验,使用类固醇和免疫抑制药物治疗是成功的。