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一名两岁儿童患布加综合征和川崎病:双重风险病例

Brugada Syndrome and Kawasaki Disease in a Two-Year-Old: A Case of Double Jeopardy.

作者信息

Boateng Jeffery O, Stein Ilana, Hidalgo Nicholas

机构信息

Pediatrics, St. Barnabas Hospital Health System, Bronx, USA.

Pediatric Cardiology, Children's Hospital at Montefiore, Bronx, USA.

出版信息

Cureus. 2024 Dec 2;16(12):e75001. doi: 10.7759/cureus.75001. eCollection 2024 Dec.

Abstract

Brugada syndrome (BrS) is a genetic channelopathy that may predispose to ventricular arrhythmia. It is inherited as an autosomal dominant pattern with incomplete penetrance. Fever can unmask Brugada syndrome in children who have a genetic predisposition. Kawasaki disease is not known to be associated with Brugada syndrome; however, it may lead to cardiac complications such as coronary artery abnormalities and myocardial inflammation. We report a case of a two-year-old who was diagnosed with Kawasaki disease and subsequently developed Brugada syndrome.

摘要

布加综合征(BrS)是一种遗传性离子通道病,可能易患室性心律失常。它以常染色体显性模式遗传,具有不完全外显率。发热可使具有遗传易感性的儿童显现出布加综合征。目前已知川崎病与布加综合征无关;然而,它可能导致心脏并发症,如冠状动脉异常和心肌炎症。我们报告一例两岁患儿,其最初被诊断为川崎病,随后发展为布加综合征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30e/11693925/0a5e968b70c9/cureus-0016-00000075001-i01.jpg

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