Kaplan Melike Mehveş, Çelikel Elif, Güngörer Vildan, Ekici Tekin Zahide, Gürsu Hazım Alper, Polat Sanem Eryılmaz, Cinel Güzin, Çelikel Acar Banu
Division of Pediatric Rheumatology, Department of Pediatrics, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.
Division of Pediatric Cardiology, Department of Pediatrics, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.
Int J Rheum Dis. 2023 Aug;26(8):1582-1585. doi: 10.1111/1756-185X.14630. Epub 2023 Feb 28.
Juvenile dermatomyositis (JDM) is an autoimmune disease characterized by muscle weakness and specific skin lesions, as well as non-muscular involvement such as interstitial lung disease (ILD), cardiac involvement and arthritis. Anti-melanoma differentiation-associated protein 5 (anti-MDA5)-positive JDM patients are typically characterized by the presence of skin ulcers and rapidly progressing ILD (RP-ILD). Although cardiac involvement is not an expected involvement in anti-MDA5-positive JDM cases, it is significant because it can be fatal. In this report, an anti-MDA5 myositis-specific autoantibody-positive JDM case referred with the diagnosis of psoriatic arthritis in whom cardiomyopathy and arrhythmia were detected in follow-up is presented. Since cardiac involvement is associated with mortality, it would be useful to follow up anti-MDA5 positive patients for cardiac involvement in addition to lung involvement. Tofacitinib is a promising treatment option in treatment-resistant JDM.
青少年皮肌炎(JDM)是一种自身免疫性疾病,其特征为肌肉无力、特定的皮肤病变以及间质性肺病(ILD)、心脏受累和关节炎等非肌肉受累情况。抗黑色素瘤分化相关蛋白5(抗MDA5)阳性的JDM患者通常表现为皮肤溃疡和快速进展性ILD(RP-ILD)。尽管心脏受累并非抗MDA5阳性JDM病例的预期受累情况,但因其可能致命而具有重要意义。在本报告中,介绍了1例抗MDA5肌炎特异性自身抗体阳性的JDM病例,该病例最初诊断为银屑病关节炎,随访中发现患有心肌病和心律失常。由于心脏受累与死亡率相关,除了肺部受累外,对抗MDA5阳性患者进行心脏受累情况的随访将很有帮助。托法替布是治疗抵抗性JDM中一种有前景的治疗选择。