A Review of MDA-5 Dermatomyositis and Associated Interstitial Lung Disease

Rheumato Pub Date : 2024-02-28 DOI:10.3390/rheumato4010004
S. Bhandari, Lisa Zickuhr, M. Baral, Sanjeev Bhalla, Heather Jones, Robert Bucelli, Deepali Sen
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Abstract

Anti-melanoma differentiation-associated gene 5 (MDA-5) dermatomyositis (DM) is noteworthy for its association with rapidly progressive interstitial lung disease (RP-ILD), vasculopathy, and distinctive cutaneous features. First identified in a Japanese cohort in 2005, MDA-5 DM carries a significant mortality risk, emphasizing the crucial need for early diagnosis. This review explores the pathogenesis, clinical presentation, diagnosis, management, and prognosis of MDA-5 DM and ILD and includes new research and recommendations regarding disease management.
MDA-5 皮肌炎及相关间质性肺病综述
抗黑色素瘤分化相关基因 5(MDA-5)皮肌炎(DM)与快速进展性间质性肺病(RP-ILD)、血管病变和独特的皮肤特征有关,值得注意。MDA-5 DM 于 2005 年首次在日本的一个队列中被发现,它具有显著的致死风险,强调了早期诊断的重要性。本综述探讨了 MDA-5 DM 和 ILD 的发病机制、临床表现、诊断、管理和预后,并包括有关疾病管理的新研究和建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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