Dermatomyositis Which Was Double Positive for Anti-MDA5 and Anti-ARS Antibodies That Was Successfully Treated by Intensive Immunosuppressive Therapy

S. Hama, M. Higashida-Konishi, M. Akiyama, T. Shimada, H. Takei, K. Izumi, H. Oshima, Y. Okano
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引用次数: 1

Abstract

Myositis-specific autoantibody is associated with the clinical phenotype and prognosis of dermatomyositis. Anti-melanoma differentiation-associated gene 5 (MDA5) and anti-aminoacyl-tRNA synthetase (ARS) antibodies are generally mutually exclusive. We herein present an extremely rare case of dermatomyositis which showed double positivity for anti-MDA5 and anti-ARS antibodies. There have been very few reported cases of double positive anti-MDA5, anti-ARS antibodies. In such cases, the clinical characteristics of each autoantibody can coexist. Thus, we should pay attention to the rapidly progressing features of anti-MDA5 as well as the chronic relapsing features of anti-ARS for the better management of this rare condition.
抗mda5和抗ars抗体双阳性,经强化免疫抑制治疗成功的皮肌炎
肌炎特异性自身抗体与皮肌炎的临床表型和预后有关。抗黑色素瘤分化相关基因5(MDA5)和抗氨酰基tRNA合成酶(ARS)抗体通常是互斥的。我们在此报告了一例极为罕见的皮肌炎病例,该病例显示抗MDA5和抗ARS抗体双重阳性。很少有报告的抗MDA5、抗ARS抗体双阳性病例。在这种情况下,每种自身抗体的临床特征可以共存。因此,我们应该注意抗MDA5的快速进展特征以及抗ARS的慢性复发特征,以便更好地治疗这种罕见的疾病。
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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