Chaisson Neal F, Paik Julie, Orbai Ana-Maria, Casciola-Rosen Livia, Fiorentino David, Danoff Sonye, Rosen Antony
From the Division of Pulmonary and Critical Care Medicine (NFC, SD) and Division of Rheumatology (JP, A-MO, LC-R, AR), Johns Hopkins University School of Medicine, Baltimore, Maryland; and Department of Dermatology (DF), Stanford University School of Medicine, Palo Alto, California.
Medicine (Baltimore). 2012 Jul;91(4):220-228. doi: 10.1097/MD.0b013e3182606f0b.
Melanoma differentiation-associated protein 5 (MDA-5) is a novel autoantibody frequently characterized by interstitial lung disease and a distinct cutaneous phenotype with palmar papules, ulceration, and rash. Virtually all patients have underlying dermatomyositis, but many lack the characteristic clinical myopathy associated with it. In the setting of amyopathic disease, the absence of clinically available biomarkers or clear pathologic diagnosis can complicate effective prognostic and therapeutic intervention. Until recently the presence of MDA-5 antibody associated dermato-pulmonary syndrome was described only in Asian populations. We present 2 cases of MDA-5-associated dermato-pulmonary syndrome and provide a comprehensive review of available literature.
黑色素瘤分化相关蛋白5(MDA-5)是一种新型自身抗体,常表现为间质性肺病以及伴有掌部丘疹、溃疡和皮疹的独特皮肤表型。几乎所有患者都有潜在的皮肌炎,但许多患者缺乏与之相关的典型临床肌病。在无肌病性疾病的情况下,缺乏临床可用的生物标志物或明确的病理诊断会使有效的预后和治疗干预变得复杂。直到最近,MDA-5抗体相关的皮肤-肺综合征仅在亚洲人群中被描述。我们报告2例MDA-5相关的皮肤-肺综合征病例,并对现有文献进行全面综述。