Roughneen P, Mahmoudian M H, Ott D A
Department of Cardiovascular Surgery, Texas Heart Institute, Houston 77225, USA.
Cardiovasc Surg. 1995 Feb;3(1):78-80. doi: 10.1016/0967-2109(95)92910-a.
The case of an infant who was born with the rare presentation of complete atrioventricular canal defect and transposition of the great arteries is described. The patient underwent pulmonary banding at the age of 2 months, followed by concomitant arterial switch and repair of the atrioventricular canal defect at 20 months. Palliative banding allowed for the infant to grow and thus facilitated the later successful repair of these congenital defects.
本文描述了一名婴儿的病例,该婴儿出生时患有罕见的完全性房室通道缺损和大动脉转位。该患者在2个月大时接受了肺动脉环扎术,随后在20个月大时接受了动脉调转术及房室通道缺损修复术。姑息性环扎术使婴儿得以成长,从而为后期成功修复这些先天性缺陷创造了条件。