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老年患者不明原因左心室肥厚伴症状性高度房室传导阻滞:一例报告

Unexplained Left Ventricular Hypertrophy with Symptomatic High-Grade Atrioventricular Block in Elderly Patients: A Case Report.

作者信息

Yu Tzu-Ping, Chen Ju-Yi

机构信息

Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan 704, Taiwan.

出版信息

J Clin Med. 2022 Jun 19;11(12):3522. doi: 10.3390/jcm11123522.

Abstract

Left ventricular hypertrophy (LVH) is common among older adults. Amidst all causes, Fabry disease (FD) should be considered when LVH occurs with family history, specific clinical manifestations, or cardiac alert signs. Here, we report a case of a 76-year-old male who presented late onset concentric LVH with symptomatic high-grade atrioventricular (AV) block. After dual-chamber pacemaker implantation, interrogation revealed frequent right ventricular (RV) pacing with a wide QRS duration. The patient developed heart failure symptoms with rapid deterioration of LV systolic function. Pacing-induced cardiomyopathy (PICM) was suspected, and the pacemaker was upgraded to biventricular pacing. Further FD surveys were performed, including biochemical examinations, cardiac biopsies, and genetic sequencing, and the patient was ultimately diagnosed with a cardiac variant of FD. Particularly, we strongly suggest that physiologic pacing should be initially considered for patients with FD who have symptomatic high-grade AV block, rather than traditional RV pacing to prevent PICM.

摘要

左心室肥厚(LVH)在老年人中很常见。在所有病因中,当LVH伴有家族史、特定临床表现或心脏警示体征时,应考虑法布里病(FD)。在此,我们报告一例76岁男性病例,该患者出现迟发性向心性LVH并伴有症状性高度房室(AV)传导阻滞。双腔起搏器植入后,程控显示右心室(RV)频繁起搏且QRS时限增宽。患者出现心力衰竭症状,LV收缩功能迅速恶化。怀疑为起搏诱导性心肌病(PICM),遂将起搏器升级为双心室起搏。进一步进行了FD相关检查,包括生化检查、心脏活检和基因测序,最终该患者被诊断为FD心脏变异型。特别地,我们强烈建议,对于有症状性高度AV传导阻滞的FD患者,应首先考虑生理性起搏,而非传统的RV起搏,以预防PICM。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caa9/9225472/3d5aef2e09ea/jcm-11-03522-g001.jpg

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