Zhang Luyan, Cheng Xueying, Chen Jinlong, Zhou Ming, Qian Tianwei, Zhang Zhongman, Yin Jie, Zhang Han, Dai Genyin, Qin Yuming, Yang Shiwei
Department of Cardiology, Children's Hospital of Nanjing Medical University, Nanjing, China.
Front Pediatr. 2020 Jun 16;8:312. doi: 10.3389/fped.2020.00312. eCollection 2020.
Hypertrophic cardiomyopathy (HCM) is a group of myocardial diseases defined by cardiac hypertrophy which cannot be explained by secondary causes with a non-dilated left ventricle and preserved or increased ejection fraction. Sometimes it can be combined with restrictive cardiomyopathy. Here we describe a very rare case of a 12-year-old girl with non-obstructive hypertrophic cardiomyopathy accompanied by restrictive phenotype, complete left bundle branch block and intermittent third-degree atrioventricular block, who presented with recurrent syncope. Her father was also found to have hypertrophic cardiomyopathy and treated with implantable cardioverter defibrillator for ventricular tachycardia. Her younger brother is currently asymptomatic but echocardiogram showed hypertrophic cardiomyopathy. Genetic analysis identified a heterozygous missense mutation (c.2155C>T, p.R719W) of in the proband girl, her father and her brother. The girl was treated with left bundle pacing and recovered well. The case we present further demonstrates the feasibility of left bundle pacing in children.
肥厚型心肌病(HCM)是一组以心肌肥厚为特征的心肌疾病,其不能用继发原因解释,左心室无扩张,射血分数正常或增加。有时可合并限制型心肌病。在此,我们描述了一例非常罕见的12岁女孩病例,她患有非梗阻性肥厚型心肌病,伴有限制型表型、完全性左束支传导阻滞和间歇性三度房室传导阻滞,表现为反复晕厥。还发现她的父亲患有肥厚型心肌病,并接受了植入式心脏复律除颤器治疗室性心动过速。她的弟弟目前无症状,但超声心动图显示有肥厚型心肌病。基因分析在患病女孩、她的父亲和弟弟中鉴定出一个杂合错义突变(c.2155C>T,p.R719W)。该女孩接受了左束支起搏治疗,恢复良好。我们展示的这个病例进一步证明了左束支起搏在儿童中的可行性。