{"title":"肝豆状核变性的Brugada心电图模式","authors":"Marios G. Bantidos MD , Panagiotis Stachteas MD, PhD(c) , Athina Nasoufidou MD, PhD(c) , Efstratios Karagiannidis MD, PhD , Varvara Fyntanidou MD, PhD , Eleni Theocharidou MD, PhD , Nikolaos Fragakis MD, PhD","doi":"10.1016/j.jaccas.2025.105233","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Wilson disease and Brugada syndrome initially appear unrelated. Although cardiac manifestations in Wilson disease are increasingly recognized, it remains controversial whether direct copper infiltration is the sole mechanism underpinning structural and electroanatomical abnormalities.</div></div><div><h3>Case Summary</h3><div>We present the case of a 40-year-old man with genetically confirmed Wilson disease who exhibited a spontaneous Brugada type 3 electrocardiographic pattern. Subsequent to a flecainide challenge, a Brugada type 1 electrocardiographic pattern was unmasked, although no prior history of arrhythmias was reported. Regular follow-up care was not accompanied by any adverse cardiac events.</div></div><div><h3>Discussion</h3><div>This is the first documented case of such a co-occurrence, to our knowledge, and it suggests a potential Wilson-induced Brugada phenocopy, possibly attributable to the mechanistic effects of copper's redox properties, which may mimic the microstructural impairment postulated in genetic Brugada syndrome.</div></div><div><h3>Take-Home Message</h3><div>Systemic metabolic disturbances variously precipitate cardiac electrical abnormalities and should be considered in atypical presentations of arrhythmia syndromes.</div></div>","PeriodicalId":14792,"journal":{"name":"JACC. Case reports","volume":"30 29","pages":"Article 105233"},"PeriodicalIF":0.0000,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Brugada ECG Pattern in Wilson Disease\",\"authors\":\"Marios G. Bantidos MD , Panagiotis Stachteas MD, PhD(c) , Athina Nasoufidou MD, PhD(c) , Efstratios Karagiannidis MD, PhD , Varvara Fyntanidou MD, PhD , Eleni Theocharidou MD, PhD , Nikolaos Fragakis MD, PhD\",\"doi\":\"10.1016/j.jaccas.2025.105233\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Wilson disease and Brugada syndrome initially appear unrelated. Although cardiac manifestations in Wilson disease are increasingly recognized, it remains controversial whether direct copper infiltration is the sole mechanism underpinning structural and electroanatomical abnormalities.</div></div><div><h3>Case Summary</h3><div>We present the case of a 40-year-old man with genetically confirmed Wilson disease who exhibited a spontaneous Brugada type 3 electrocardiographic pattern. Subsequent to a flecainide challenge, a Brugada type 1 electrocardiographic pattern was unmasked, although no prior history of arrhythmias was reported. Regular follow-up care was not accompanied by any adverse cardiac events.</div></div><div><h3>Discussion</h3><div>This is the first documented case of such a co-occurrence, to our knowledge, and it suggests a potential Wilson-induced Brugada phenocopy, possibly attributable to the mechanistic effects of copper's redox properties, which may mimic the microstructural impairment postulated in genetic Brugada syndrome.</div></div><div><h3>Take-Home Message</h3><div>Systemic metabolic disturbances variously precipitate cardiac electrical abnormalities and should be considered in atypical presentations of arrhythmia syndromes.</div></div>\",\"PeriodicalId\":14792,\"journal\":{\"name\":\"JACC. Case reports\",\"volume\":\"30 29\",\"pages\":\"Article 105233\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-09-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JACC. Case reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666084925020133\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JACC. Case reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666084925020133","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Wilson disease and Brugada syndrome initially appear unrelated. Although cardiac manifestations in Wilson disease are increasingly recognized, it remains controversial whether direct copper infiltration is the sole mechanism underpinning structural and electroanatomical abnormalities.
Case Summary
We present the case of a 40-year-old man with genetically confirmed Wilson disease who exhibited a spontaneous Brugada type 3 electrocardiographic pattern. Subsequent to a flecainide challenge, a Brugada type 1 electrocardiographic pattern was unmasked, although no prior history of arrhythmias was reported. Regular follow-up care was not accompanied by any adverse cardiac events.
Discussion
This is the first documented case of such a co-occurrence, to our knowledge, and it suggests a potential Wilson-induced Brugada phenocopy, possibly attributable to the mechanistic effects of copper's redox properties, which may mimic the microstructural impairment postulated in genetic Brugada syndrome.
Take-Home Message
Systemic metabolic disturbances variously precipitate cardiac electrical abnormalities and should be considered in atypical presentations of arrhythmia syndromes.