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小儿患者房扑揭示的SCN5A突变相关病态窦房结综合征

SCN5A mutation-associated sick sinus syndrome revealed by atrial flutter in a pediatric patient.

作者信息

Takeda Yoshikatsu, Fujita Shuhei, Yachi Yusuke, Honda Mariko, Iwata Mayu, Sakumura Naoto, Ueno Kazuyuki, Miyashita Kengo, Futatani Takeshi, Usuda Keisuke, Chikata Akio, Usuda Kazuo, Nishida Keigo, Araki Raita, Kato Koichi, Ohno Seiko

机构信息

Department of Pediatrics, Toyama Prefectural Central Hospital, Toyama, Japan.

Department of Pediatrics, Ishikawa Prefectural Central Hospital, Ishikawa, Japan.

出版信息

J Cardiol Cases. 2025 Apr 2;32(1):5-9. doi: 10.1016/j.jccase.2025.03.001. eCollection 2025 Jul.

Abstract

UNLABELLED

Atrial flutter (AFL) is uncommon in children without underlying heart disease. This report details the case of a 7-year-old boy with AFL detected during school electrocardiogram (ECG) screening. He had no prior arrhythmias, congenital heart disease, or cardiomyopathy. Initial evaluations showed AFL with right bundle branch block but no structural heart abnormalities. Radiofrequency catheter ablation (RFCA) was performed, initially resolving the AFL but resulting in a 13-s sinus arrest requiring atrial pacing. Post-RFCA, the patient experienced a sinus arrest lasting up to 7 s, leading to a diagnosis of sick sinus syndrome (SSS). A second RFCA was needed due to AFL recurrence, and post-ablation ECGs revealed saddleback-type ST-segment elevation and Brugada-type patterns, raising suspicion of Brugada syndrome (BrS). Genetic testing identified a loss-of-function (LOF) SCN5A variant (c.2678G > A p.R893H) in the patient, his mother, and his sister. This case underscores that AFL in children without structural heart disease, especially when associated with SSS, may be linked to LOF SCN5A variants, which are also associated with BrS.

LEARNING OBJECTIVE

Atrial flutter in children without structural heart disease can be linked to genetic factors with Brugada syndrome (BrS). This case highlights the importance of thorough diagnostic evaluation, including family history and genetic testing, when rare arrhythmias are present. Early detection of BrS through detailed electrocardiographic findings and family screening can help identify at-risk individuals and guide appropriate management to prevent serious arrhythmias and sudden cardiac death.

摘要

未标记

心房扑动(AFL)在无潜在心脏病的儿童中并不常见。本报告详细介绍了一名7岁男孩在学校心电图(ECG)筛查中被检测出患有AFL的病例。他既往无心律失常、先天性心脏病或心肌病。初步评估显示为伴有右束支传导阻滞的AFL,但无结构性心脏异常。进行了射频导管消融术(RFCA),最初解决了AFL,但导致了13秒的窦性停搏,需要进行心房起搏。RFCA术后,患者经历了长达7秒的窦性停搏,导致诊断为病态窦房结综合征(SSS)。由于AFL复发,需要进行第二次RFCA,消融术后的心电图显示鞍背型ST段抬高和Brugada型图形,引发了对Brugada综合征(BrS)的怀疑。基因检测在患者及其母亲和妹妹中发现了功能丧失(LOF)的SCN5A变异(c.2678G>A p.R893H)。该病例强调,无结构性心脏病的儿童中的AFL,尤其是与SSS相关时,可能与LOF SCN5A变异有关,而这些变异也与BrS有关。

学习目标

无结构性心脏病的儿童中的心房扑动可能与Brugada综合征(BrS)的遗传因素有关。该病例突出了在出现罕见心律失常时进行全面诊断评估的重要性,包括家族史和基因检测。通过详细的心电图检查结果和家族筛查早期发现BrS有助于识别高危个体,并指导适当的管理以预防严重心律失常和心源性猝死。

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Brugada syndrome and sinus node dysfunction.Brugada综合征与窦房结功能障碍。
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Atrial flutter in the young: a collaborative study of 380 cases.
J Am Coll Cardiol. 1985 Oct;6(4):871-8. doi: 10.1016/s0735-1097(85)80497-6.

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