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[肺动脉闭锁伴肺分支严重发育不全。根治性两期矫正术]

[Pulmonary atresia with major hypoplasia of the pulmonary branches. A radical 2-stage correction].

作者信息

Iselin M, Grollier G, Pelouze G A, Couetil J P, Fauchon G, Foucault J P, Khayat A

出版信息

Arch Mal Coeur Vaiss. 1983 May;76(5):524-9.

PMID:6411024
Abstract

Pulmonary atresia with ventricular septal defect (VSD) and severe hypoplasia of the pulmonary branches is a serious malformation and reputedly inoperable. The surgical restoration of a pulmonary outflow tract may nevertheless dilate the pulmonary arterial branches in the long term. The probable mechanism of this effect is related to high right ventricular and pulmonary pulse pressures due to the absence of the pulmonary valve. The right to left shunt, initially, reverses after a few weeks so authorizing closure of the VSD. Two patients, an adult and a child, were successfully treated by this technique.

摘要

肺动脉闭锁合并室间隔缺损及严重肺分支发育不全是一种严重畸形,据说无法手术治疗。然而,从长期来看,肺动脉流出道的手术重建可能会使肺动脉分支扩张。这种效应的可能机制与因肺动脉瓣缺失导致的右心室和肺脉压升高有关。最初的右向左分流在几周后会逆转,从而能够闭合室间隔缺损。一名成人和一名儿童患者通过该技术成功得到治疗。

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