川崎病伴有持续严重的银屑病样皮肤表现和心源性猝死

IF 1.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Aso F. Salih , Trifa M. Qadir , Nagib Dahdah
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引用次数: 0

摘要

本病例报告描述了一名1.3岁婴儿在家庭成员暴露于COVID-19和SARS-CoV-2 IgG抗体阳性后出现不典型川崎病(KD)的症状。临床表现为明显的左心室功能障碍,进行性冠状动脉受累,并伴有严重的皮肤症状,包括史蒂文-约翰逊样病变和银屑病样皮疹。尽管最初心脏功能有所改善,但婴儿出现了多个冠状动脉瘤并死于心源性猝死。该病例强调了在COVID-19背景下管理非典型KD的诊断和治疗挑战。我们描述的情况下,回顾文献相关的严重皮肤病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kawasaki disease with persistent severe psoriatic-like skin manifestations and sudden cardiac death
This case report describes a 1.3-year-old infant with an atypical presentation of Kawasaki Disease (KD) following exposure to COVID-19 within the family and positive SARS-CoV-2 IgG antibodies. The clinical course was marked by significant left ventricular (LV) dysfunction, progressive coronary artery involvement, and complicated by severe dermatologic manifestations including Steven-Johnson-like lesions and psoriatic-like eruptions. Despite initial improvement in cardiac function, the infant developed multiple coronary aneurysms and succumbed to sudden cardiac death. This case highlights the diagnostic and therapeutic challenges in managing atypical KD in the context of COVID-19. We describe the case and review the literature related to the associated severe skin lesions.
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来源期刊
International journal of cardiology. Congenital heart disease
International journal of cardiology. Congenital heart disease Cardiology and Cardiovascular Medicine
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83 days
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