Department of Rheumatology, Fukushima Medical University School of Medicine, Japan.
Department of Internal Medicine, Ohara General Hospital, Japan.
Intern Med. 2024;63(10):1473-1478. doi: 10.2169/internalmedicine.2382-23. Epub 2024 May 15.
Anti-melanoma differentiation-associated gene 5 (MDA5) antibody-positive clinically amyopathic dermatomyositis (CADM) is a subtype of dermatomyositis without severe myositis but with characteristic cutaneous manifestations and severe interstitial lung disease. Joint symptoms can occur in patients with anti-MDA5 antibody-positive CADM. However, the treatment strategy and utility of ultrasound for treating joint symptoms remain unknown. We herein report an 85-year-old man with anti-MDA5 antibody-positive CADM who presented with ultrasound-confirmed synovitis that improved with medium-dose corticosteroid therapy.
抗黑色素瘤分化相关基因 5(MDA5)抗体阳性的临床无肌病性皮肌炎(CADM)是皮肌炎的一种亚型,无严重肌炎,但有特征性皮肤表现和严重的间质性肺病。抗 MDA5 抗体阳性 CADM 患者可出现关节症状。然而,关节症状的治疗策略和超声的应用仍不清楚。本文报告了一例 85 岁男性抗 MDA5 抗体阳性 CADM 患者,其关节超声证实存在滑膜炎,中剂量皮质类固醇治疗后改善。