儿茶酚胺能多态性室性心动过速
医学
离子通道病
致心律失常性右心室发育不良
Brugada综合征
心脏病学
内科学
心源性猝死
肥厚性心肌病
短QT综合征
猝死
长QT综合征
心室颤动
室性心动过速
心脏骤停
兰尼碱受体2
心肌病
QT间期
心力衰竭
兰尼定受体
钙
作者
Jason D. Heiner,Jeffrey H. Bullard-Berent,Shmuel Inbar
标识
DOI:10.1097/pec.0b013e3182360606
摘要
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare adrenergically mediated arrhythmogenic disorder classically induced by exercise or emotional stress and found in structurally normal hearts. It is an important cause of cardiac syncope and sudden death in childhood. Catecholaminergic polymorphic ventricular tachycardia is a genetic cardiac channelopathy with known mutations involving genes affecting intracellular calcium regulation. We present a case of a 14-year-old boy who had cardiopulmonary arrest after an emotionally induced episode of CPVT while attempting to invite a girl to the school dance. Review of his presenting cardiac rhythm, induction of concerning ventricular arrhythmias during an exercise stress test, and genetic testing confirmed the diagnosis of CPVT. He recovered fully and was treated with β-blocker therapy and placement of an implantable cardioverter-defibrillator. In this report, we discuss this rare but important entity, including its molecular foundation, clinical presentation, basics of diagnosis, therapeutic options, and implications of genetic testing for family members. We also compare CPVT to other notable cardiomyopathic and channelopathic causes of sudden death in youth including hypertrophic cardiomyopathy, arrhythmogenic right ventricular dysplasia, long QT syndrome, short QT syndrome, and Brugada syndrome.
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