本特尔手术治疗单尖瓣主动脉瓣畸形1例

Q3 Medicine
Sung Joon Park, Jae Hoon Lee, E. Chung
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引用次数: 1

摘要

单尖瓣主动脉瓣是一种罕见的先天性畸形,通常表现为瓣膜功能障碍和扩张或主动脉瘤,需要联合主动脉瓣手术和主动脉修复。一些患者表现出严重的瓣膜钙化延伸至室间隔,可能导致瓣膜置换术清创时传导系统受损。我们报告一位36岁男性患者,术前经食管超声心动图诊断为严重主动脉瓣狭窄伴单瓣单尖瓣。复合移植物置换主动脉瓣、主动脉根和升主动脉后,由于术后完全性心脏传导阻滞,放置永久性起搏器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bentall Operation in a Patient with a Unicommissural Unicuspid Aortic Valve
A unicuspid aortic valve is a rare congenital malformation that frequently presents with valvular dysfunction and dilatation or aortic aneurysm, requiring combined aortic valve surgery and aortic repair. Some patients show severe valve calcification extending into the interventricular septum, possibly resulting in damage to the conduction system during debridement for valve replacement. We present a rare case of severe aortic stenosis with a unicommissural unicuspid aortic valve diagnosed by preoperative transesophageal echocardiography in a 36-year-old man. After composite graft replacement of the aortic valve, aortic root, and ascending aorta, a permanent pacemaker was placed because of postoperative complete heart block.
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