一份心电图改变了一名小男孩的人生：致心律失常性右室发育不良病例
An ECG changed the life of a young boy: a case of arrhythmogenic right ventricular dysplasia.
作者信息
Altun Ibrahim, Akin Fatih, Sahin Cem, Beydilli Halil
机构信息
Department of Cardiology, Mugla Sitki Kocman University Medical Faculty, Mugla, Turkey.
Department of Internal Medicine, Mugla University Medical Faculty, Mugla, Turkey.
出版信息
BMJ Case Rep. 2014 Oct 24;2014:bcr2014204703. doi: 10.1136/bcr-2014-204703.
Arrhythmogenic right ventricular dysplasia (ARVD) is a progressive condition with the right ventricular myocardium being replaced by fibrofatty tissue. It is a hereditary disorder mostly caused by desmosome gene mutations. The prevalence of arrhythmogenic right ventricular cardiomyopathy is about 1/1000-5000. Clinical presentation is usually related to ventricular tachycardias, syncope, presyncope or ventricular fibrillation leading to cardiac arrest, mostly in young people and athletes. We report a case of a 17-year-old boy from Turkey, who was referred to our cardiology department for an ECG, required of him prior to joining a football team.
致心律失常性右室心肌病（ARVD）是一种进行性疾病，其右心室心肌被纤维脂肪组织替代。它是一种遗传性疾病，主要由桥粒基因突变引起。致心律失常性右室心肌病的患病率约为1/1000 - 5000。临床表现通常与室性心动过速、晕厥、先兆晕厥或导致心脏骤停的心室颤动有关，多见于年轻人和运动员。我们报告一例来自土耳其的17岁男孩，他因加入足球队前需进行心电图检查而被转诊至我们的心脏病科。
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