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成功修复合并二尖瓣反流和心房颤动的成人三房心:一例报告

Successfully repaired adult cor triatriatum with mitral regurgitation and atrial fibrillation: a case report.

作者信息

Naito Shuhei, Enomoto Yoshiharu, Morizumi Sei, Kaminishi Yuichiro, Mathis Bryan J, Suzuki Yasuyuki

机构信息

Department of Cardiovascular Surgery, Ibaraki Prefectural Central Hospital, 6528 Koibuchi, Kasama, Ibaraki, Japan.

Department of Cardiovascular Surgery, Institute of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8575, Japan.

出版信息

Gen Thorac Cardiovasc Surg Cases. 2025 Apr 7;4(1):22. doi: 10.1186/s44215-025-00206-5.

Abstract

BACKGROUND

Rarely seen in adults, cor triatriatum is a congenital defect in which a membrane creates three atrial chambers in the heart. Atrial fibrillation (AF) is the most common complication, but repair procedures in adults remain unestablished.

CASE PRESENTATION

A 49-year-old woman had cor triatriatum sinister (Lucas-Schmidt classification type I-A) with moderate mitral regurgitation and atrial fibrillation. Communication between the accessory chamber and the main chamber was established via a 10-mm fenestration with a pressure gradient of 14 mmHg. Mitral valve repair and the maze procedure, via radiofrequency ablation, was done after complete resection of the anomalous septum in the left atrium. Mitral regurgitation was well-controlled and atrial fibrillation disappeared. Sinus rhythm has been continually maintained at 6 months post-surgery, with no mitral regurgitation recurrence.

CONCLUSIONS

Here, a rare adult cor triatriatum case with simultaneous mitral valve regurgitation and atrial fibrillation was treated with good results. The maze procedure shows effectiveness for atrial fibrillation associated with cor triatriatum. Especially the anomalous membrane attachments must be resolved in addition to the conventional maze procedure because electrical mapping of Cor triatriatum sinister showed low-voltage zones at the membrane attachments and it cause macro-reentrant atrial tachycardia.

摘要

背景

三房心在成年人中罕见,是一种先天性缺陷,即心脏中由一层膜形成三个心房腔。心房颤动(AF)是最常见的并发症,但成人的修复手术仍未确立。

病例报告

一名49岁女性患有左位三房心(卢卡斯 - 施密特分类I - A型),伴有中度二尖瓣反流和心房颤动。通过一个10毫米的开窗建立副房与主房之间的交通,压力阶差为14毫米汞柱。在完全切除左心房异常隔膜后,进行了二尖瓣修复和迷宫手术(通过射频消融)。二尖瓣反流得到良好控制,心房颤动消失。术后6个月持续维持窦性心律,无二尖瓣反流复发。

结论

在此,一例罕见的同时伴有二尖瓣反流和心房颤动的成年三房心病例得到了良好治疗效果。迷宫手术对与三房心相关的心房颤动显示出有效性。特别是除了传统的迷宫手术外,必须解决异常膜附着问题,因为左位三房心的电标测显示膜附着处存在低电压区,这会导致大折返性房性心动过速。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/702c/11978175/4df3239000c2/44215_2025_206_Fig1_HTML.jpg

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