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[1例先天性三尖瓣反流合并房间隔缺损及周围性肺动脉狭窄]

[A case of congenital tricuspid regurgitation associated with atrial septal defect and peripheral pulmonary stenosis].

作者信息

Tanji M, Iwaya F, Igari T, Ogawa T, Takahashi K, Hoshino S

机构信息

Department of Cardiovascular Surgery, Fukushima Medical College, Japan.

出版信息

Nihon Kyobu Geka Gakkai Zasshi. 1996 Dec;44(12):2146-50.

PMID:8990887
Abstract

This report describes a 5-year-old girl with congenital tricuspid regurgitation associated with an atrial septal defect and peripheral pulmonary stenosis. The girl was diagnosed with the heart murmur at birth and recently developed the cardiomegaly. Cardiac echocardiography and catheterization showed severe tricuspid regurgitation, an atrial septal defect of the secundum type and peripheral pulmonary stenosis. In the operative findings, the tricuspid annulus was dilated to 33 mm in diameter, and leaflets were attached normally to the antomic annulus. There was a large cleft of the anterior leaflet of the tricuspid valve. Suture of the cleft and annuloplasty of the tricuspid valve, suture closure of the atrial septal defect and patch dilatation of peripheral pulmonary stenosis were successfully performed. Including this case, 19 other cases with congenital tricuspid regurgitation undergoing surgery were reported to date.

摘要

本报告描述了一名5岁女孩,患有先天性三尖瓣反流,并伴有房间隔缺损和外周肺动脉狭窄。该女孩出生时被诊断出心脏杂音,最近出现了心脏肥大。心脏超声心动图和心导管检查显示严重三尖瓣反流、继发孔型房间隔缺损和外周肺动脉狭窄。手术所见,三尖瓣环直径扩大至33毫米,瓣叶正常附着于解剖学上的瓣环。三尖瓣前叶有一个大的裂隙。成功进行了裂隙缝合和三尖瓣瓣环成形术、房间隔缺损缝合关闭以及外周肺动脉狭窄补片扩张术。截至目前,包括该病例在内,已有19例先天性三尖瓣反流患者接受了手术治疗并被报道。

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