医学
皮肌炎
皮肤病科
鞭笞
间质性肺病
疾病
红斑
吗啡
结缔组织病
皮肤损伤
罕见病
黑皮病
全身性疾病
肌肉疾病
病理
自身免疫性疾病
作者
Ekaterina Korytnikova,Anastasiia Sumenkova,Victor Cazac,Patrick Webster,Charles L. Halasz
出处
期刊:Skin
[National Society for Cutaneous Medicine]
日期:2025-11-10
卷期号:9 (6): 2781-2785
摘要
Anti–melanoma differentiation-associated gene 5 (MDA5) antibody-positive dermatomyositis (DM) is a rare subtype of clinically amyopathic DM characterized by minimal muscle involvement, variable skin manifestations, and a high risk of rapidly progressive interstitial lung disease (RP-ILD). Atypical skin findings are frequently misdiagnosed, delaying recognition and treatment. We present the case of a 46-year-old Black woman who developed flagellate erythema, facilitating diagnosis of anti-MDA5 DM complicated by RP-ILD. This case highlights the importance of recognizing uncommon skin findings like flagellate erythema, especially in patients with subtle or atypical presentations, and emphasizes the importance of early diagnosis and prompt immunosuppressive therapy to improve clinical outcomes.
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