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酷似室间隔完整型肺动脉闭锁的先天性三尖瓣关闭不全:两例报告

Congenital tricuspid incompetence simulating pulmonary atresia with intact ventricular septum: a report of two cases.

作者信息

Berman W, Whitman V, Stanger P, Rudolph A M

出版信息

Am Heart J. 1978 Nov;96(5):655-61. doi: 10.1016/0002-8703(78)90203-x.

Abstract

Two infants with isolated congenital tricuspid incompetence appeared to have associated right ventricular outflow tract obstruction at diagnostic evaluation, including catheterization and cineangiography. One infant died during surgery; the other improved rapidly and survived with medical therapy. We discuss the problem of establishing the presence of patency of the right ventricular outflow tract in infants with massive tricuspid incompetence and outline an approach to the management of infants whose diagnosis remains unclear even after careful evaluation.

摘要

两名患有孤立性先天性三尖瓣关闭不全的婴儿在诊断评估(包括心导管检查和心血管造影)时似乎伴有右心室流出道梗阻。一名婴儿在手术期间死亡;另一名婴儿迅速好转并通过药物治疗存活下来。我们讨论了在患有严重三尖瓣关闭不全的婴儿中确定右心室流出道通畅情况的问题,并概述了对即使经过仔细评估诊断仍不明确的婴儿的处理方法。

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