Xiao Ping-Ping, Fan Wei, Chen Xu-Yan, Li Ke-Cong, Li Ting-Ting, Dong Zhi-Gao
Department of Hematology and Rheumatology, The Second Affiliated Hospital of Xiamen Medical College, Xiamen, China.
Department of Thoracic Oncology, The Second Affiliated Hospital of Xiamen Medical College, Xiamen, China.
Front Med (Lausanne). 2024 Dec 16;11:1482350. doi: 10.3389/fmed.2024.1482350. eCollection 2024.
Melanoma differentiation-associated gene 5 (MDA5)-positive dermatomyositis (DM) is a rare systemic autoimmune disease associated with a high rate of mortality attributable to rapidly progressive interstitial lung disease. MDA5-positive DM is often complicated by a typical rash and muscle weakness. Herein, we describe a 50-year-old woman who presented with worsening pulmonary symptoms with an absence of typical clinical characteristics. We also review the treatments and prognosis made in similar cases, highlighting that closer attention should be paid to patients presenting with atypical DM, particularly when clinical manifestations such as rash and muscle weakness are not apparent.
黑色素瘤分化相关基因5(MDA5)阳性皮肌炎(DM)是一种罕见的全身性自身免疫性疾病,与快速进展性间质性肺病导致的高死亡率相关。MDA5阳性DM常伴有典型皮疹和肌无力。在此,我们描述了一名50岁女性,她出现了肺部症状恶化但缺乏典型临床特征。我们还回顾了类似病例的治疗和预后情况,强调对于表现为非典型DM的患者应给予更密切关注,尤其是当皮疹和肌无力等临床表现不明显时。