Wongjirattikarn Rachot, Chaowattanapanit Suteeraporn, Choonhakarn Charoen, So-Ngern Apichart, Mahakkanukrauh Ajanee, Foocharoen Chingching
Division of Dermatology, Department of Medicine, Faculty of Medicine, Srinagarind Hospital, Khon Kaen University, Khon Kaen, Thailand.
Division of Sleep Medicine, Department of Medicine, Faculty of Medicine, Srinagarind Hospital, Khon Kaen University, Khon Kaen, Thailand.
Case Rep Dermatol. 2020 Mar 20;12(1):57-63. doi: 10.1159/000506668. eCollection 2020 Jan-Apr.
Rapidly progressive interstitial lung disease (RP-ILD) and its distinctive cutaneous features are highly associated with the presence of anti-melanoma differentiation-associated gene 5 (anti-MDA5) antibody in patients with dermatomyositis (DM), leading to a poor prognosis. We describe the case of a 25-year-old man who developed progressive proximal muscle weakness with RP-ILD and had unusual cutaneous findings (cutaneous ulcerations and livedo reticularis) accompanied by classical cutaneous features (heliotrope rash, Gottron's papules, Gottron's sign, and flagellate erythema). Blood test was positive for anti-MDA5 antibody. He was treated with intravenous corticosteroids and immunoglobulin, but passed away due to respiratory failure within 1 month after admission. Our case highlights that the presence of cutaneous ulcerations and livedo reticularis, in addition to RP-ILD, are useful clinical clues that may aid in the detection of anti-MDA5 antibody, early initiation of combined immunosuppressants, and prognosis prediction in patients with classical DM.
快速进展性间质性肺病(RP-ILD)及其独特的皮肤特征与皮肌炎(DM)患者中抗黑色素瘤分化相关基因5(抗MDA5)抗体的存在高度相关,导致预后不良。我们描述了一名25岁男性的病例,他出现了伴有RP-ILD的进行性近端肌无力,并伴有不寻常的皮肤表现(皮肤溃疡和网状青斑)以及典型的皮肤特征(向阳疹、Gottron丘疹、Gottron征和鞭状红斑)。血液检查抗MDA5抗体呈阳性。他接受了静脉注射皮质类固醇和免疫球蛋白治疗,但入院后1个月内因呼吸衰竭去世。我们的病例强调,除了RP-ILD外,皮肤溃疡和网状青斑的存在是有用的临床线索,可能有助于检测抗MDA5抗体、早期启动联合免疫抑制剂以及预测典型DM患者的预后。