类风湿性关节炎伴有抗信号识别粒子免疫介导的坏死性肌病:病例报告。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Mohamed Reda Belkhribchia, Johannes Alexander Lobrinus, Lamyaa Semlil, Nicolas Chauveau, Abdelaziz Ajrinija, Kristof Egervari, Zine Elabidine Ennhaili
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引用次数: 0

摘要

免疫介导的坏死性肌病(IMNM)是特发性炎症性肌病的一种罕见亚型,其特征是严重的亚急性近端无力、肌纤维坏死和血清肌酸激酶显著升高。在约三分之二的 IMNM 患者中发现了抗信号识别颗粒(SRP)和抗 3-羟基-3-甲基戊二酰辅酶-A 还原酶自身抗体。这种肌病通常是特发性的,有关它与结缔组织疾病相关的文献很少。在此,我们报告了一个不寻常的病例:一名年轻女性同时患有类风湿性关节炎和严重的抗 SRP IMNM。由于采用了利妥昔单抗和环磷酰胺联合治疗方案,她的病情得到了明显改善,而且没有观察到严重的副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rheumatoid Arthritis Associated With Anti-Signal Recognition Particle Immune-Mediated Necrotizing Myopathy: A Case Report.

Immune-mediated necrotizing myopathy (IMNM) is a rare subtype of idiopathic inflammatory myopathy that is characterized by severe subacute proximal weakness, myofiber necrosis, and significantly elevated serum creatine kinase. Anti-signal recognition particle (SRP) and anti-3-hydroxy-3-methylglutaryl-coenzyme-A reductase autoantibodies have been found in about two-thirds of patients with IMNM. This myopathy is usually idiopathic and there is a scarce literature concerning its association with connective tissue diseases. Herein, we report an unusual case of a young woman who presented with both rheumatoid arthritis and severe anti-SRP IMNM. Thankfully to a therapeutic protocol combining rituximab and cyclophosphamide, an important improvement was achieved, and notably no serious side effect was observed.

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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
165
审稿时长
12 weeks
期刊介绍: The AFMR is committed to enhancing the training and career development of our members and to furthering its mission to facilitate the conduct of research to improve medical care. Case reports represent an important avenue for trainees (interns, residents, and fellows) and early-stage faculty to demonstrate productive, scholarly activity.
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