Severe pulmonary valve stenosis associated with advanced atrioventricular conduction disease: A rare case report.

IF 0.8 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Annals of Pediatric Cardiology Pub Date : 2026-09-01 Epub Date: 2026-09-08 DOI:10.4103/apc.apc_118_26
Arshad Nazir, Roopali Khanna, Shubham Srivastava, Aditya Kapoor
{"title":"Severe pulmonary valve stenosis associated with advanced atrioventricular conduction disease: A rare case report.","authors":"Arshad Nazir, Roopali Khanna, Shubham Srivastava, Aditya Kapoor","doi":"10.4103/apc.apc_118_26","DOIUrl":null,"url":null,"abstract":"<p><p>Congenital pulmonary valve stenosis is a common cause of right ventricular (RV) outflow tract obstruction. Advanced atrioventricular (AV) block in congenital heart disease is usually associated with abnormalities of AV septation or conduction system malposition. An association between isolated pulmonary valve stenosis and advanced AV block has not previously been reported. A 16-year-old male presented with exertional dyspnea and recurrent presyncope. Electrocardiography (ECG) revealed 2:1 AV block. Transthoracic echocardiography demonstrated severe valvular pulmonary stenosis with a peak gradient of 100 mmHg and preserved RV function. Cardiac computed tomography confirmed thickened pulmonary valve cusps with poststenotic pulmonary artery dilatation. The patient underwent successful balloon pulmonary valvotomy with significant reduction in RV systolic pressure. As advanced AV block persisted, a dual-chamber permanent pacemaker was implanted. The patient remained asymptomatic on follow-up. This case describes a rare and previously unreported association of advanced AV congenital heart block with isolated pulmonary valve stenosis. Persistence of heart block following relief of RV outflow obstruction suggests an underlying congenital conduction system abnormality. Awareness of this potential association is important when evaluating symptomatic patients with congenital right-sided obstructive lesions.</p>","PeriodicalId":8026,"journal":{"name":"Annals of Pediatric Cardiology","volume":"19 5","pages":"564-567"},"PeriodicalIF":0.8000,"publicationDate":"2026-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13626622/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Pediatric Cardiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/apc.apc_118_26","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/8 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0

Abstract

Congenital pulmonary valve stenosis is a common cause of right ventricular (RV) outflow tract obstruction. Advanced atrioventricular (AV) block in congenital heart disease is usually associated with abnormalities of AV septation or conduction system malposition. An association between isolated pulmonary valve stenosis and advanced AV block has not previously been reported. A 16-year-old male presented with exertional dyspnea and recurrent presyncope. Electrocardiography (ECG) revealed 2:1 AV block. Transthoracic echocardiography demonstrated severe valvular pulmonary stenosis with a peak gradient of 100 mmHg and preserved RV function. Cardiac computed tomography confirmed thickened pulmonary valve cusps with poststenotic pulmonary artery dilatation. The patient underwent successful balloon pulmonary valvotomy with significant reduction in RV systolic pressure. As advanced AV block persisted, a dual-chamber permanent pacemaker was implanted. The patient remained asymptomatic on follow-up. This case describes a rare and previously unreported association of advanced AV congenital heart block with isolated pulmonary valve stenosis. Persistence of heart block following relief of RV outflow obstruction suggests an underlying congenital conduction system abnormality. Awareness of this potential association is important when evaluating symptomatic patients with congenital right-sided obstructive lesions.

严重肺动脉瓣狭窄合并晚期房室传导疾病1例罕见报告。
先天性肺动脉瓣狭窄是右心室流出道梗阻的常见原因。先天性心脏病的晚期房室传导阻滞通常与房室分隔异常或传导系统错位有关。孤立性肺动脉瓣狭窄与晚期房室传导阻滞之间的关联此前未见报道。一个16岁的男性表现为用力呼吸困难和复发性晕厥前。心电图显示2:1房室传导阻滞。经胸超声心动图显示严重的瓣膜性肺动脉狭窄,峰值梯度为100 mmHg,右心室功能保留。心脏计算机断层扫描证实肺动脉瓣尖增厚伴狭窄后肺动脉扩张。患者成功行球囊肺瓣切开术,右心室收缩压显著降低。由于房颤阻滞持续,植入双腔永久性起搏器。随访时患者无症状。本病例描述了一个罕见且以前未报道的晚期房室先天性心脏传导阻滞与孤立性肺动脉瓣狭窄的关联。右心室流出梗阻解除后持续出现心脏传导阻滞提示潜在的先天性传导系统异常。在评估有先天性右侧阻塞性病变的有症状患者时,意识到这种潜在的关联是很重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Annals of Pediatric Cardiology
Annals of Pediatric Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
1.40
自引率
14.30%
发文量
51
审稿时长
23 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书