Deadly Proposal A Case of Catecholaminergic Polymorphic Ventricular Tachycardia

被引:3
作者
Heiner, Jason D. [1 ]
Bullard-Berent, Jeffrey H. [2 ,3 ]
Inbar, Shmuel [4 ]
机构
[1] Brooke Army Med Ctr, Dept Emergency Med, San Antonio, TX USA
[2] Mary Bridge Childrens Hosp, Dept Emergency Med, Tacoma, WA USA
[3] Univ New Mexico, Div Cardiol, Dept Emergency Med, Albuquerque, NM 87131 USA
[4] Univ New Mexico, Div Cardiol, Dept Internal Med, Albuquerque, NM 87131 USA
关键词
catecholaminergic polymorphic ventricular tachycardia; CPVT; ventricular tachycardia; sudden death; clinical genetics; CARDIAC RYANODINE RECEPTOR; SUDDEN UNEXPLAINED DEATH; BRUGADA-SYNDROME; MOLECULAR AUTOPSY; FOLLOW-UP; ARREST; MUTATIONS; CHILDREN; SYNCOPE; DIAGNOSIS;
D O I
10.1097/PEC.0b013e3182360606
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
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 beta-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.
引用
收藏
页码:1065 / 1068
页数:4
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