Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Mod Rheumatol Case Rep. 2020 Jan;4(1):1-5. doi: 10.1080/24725625.2019.1628427. Epub 2019 Jun 24.
A 66-year old woman with a 14-year history of rheumatoid arthritis (RA) and uveitis was admitted to our department for evaluation of a mass in the left neck. Fourteen months prior to this admission the patient was started on golimumab. Serum creatine kinase (CK) level was elevated and myositis-specific and -associated antibodies were negative. Manual muscle test showed weakness in the neck flexor, sternocleidomastoid and deltoid muscles. Magnetic resonance imaging (MRI) of the neck, erector muscle of spine, breech, thigh and lower thigh demonstrated high-intensity lesions in the muscles in short-tau inversion recovery images. Electromyography in the right deltoid detected fibrillation potentials. Muscle biopsy from the left neck mass showed granulomatous myositis. Muscle weakness improved and CK levels normalized after discontinuation of golimumab. We report a case of granulomatous myositis under anti-TNF-α treatment for RA.
一位 66 岁女性,类风湿关节炎(RA)病史 14 年,伴葡萄膜炎,因左颈部肿块收入我科。此次入院前 14 个月,患者开始使用戈利木单抗治疗。血清肌酸激酶(CK)升高,肌炎特异性和相关性抗体阴性。徒手肌力检查显示颈部屈肌、胸锁乳突肌和三角肌无力。颈部、脊柱竖脊肌、臀部、大腿和大腿下部磁共振成像(MRI)显示短回波反转恢复图像中肌肉高信号病变。右侧三角肌肌电图检测到纤颤电位。左颈部肿块肌肉活检显示肉芽肿性肌炎。停用戈利木单抗后,肌肉无力改善,CK 水平恢复正常。我们报告了一例抗 TNF-α 治疗 RA 后发生的肉芽肿性肌炎。