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肺动脉闭锁合并完整室间隔:一种修订分类法。

Pulmonary atresia and intact ventricular septum: a revised classification.

作者信息

Bull C, de Leval M R, Mercanti C, Macartney F J, Anderson R H

出版信息

Circulation. 1982 Aug;66(2):266-72. doi: 10.1161/01.cir.66.2.266.

Abstract

The dismal outlook for patients with pulmonary atresia with intact ventricular septum may be related to associated right ventricular hypoplasia. Study of 32 autopsy specimens and 46 angiocardiograms of neonates with this lesion suggested that the cavitary hypoplasia was related to massive hypertrophy of the right ventricular wall. This hypertrophy was sufficient to obliterate the trabecular and/or infundibular portion of the ventricular cavity entirely in one-third of the cases; this observation forms the basis for a revised classification of these hearts. Three autopsies and 14 angiograms of neonates with critical pulmonary stenosis were examined. Hearts with obliterated infundibular and trabecular cavities had thicker walls and smaller tricuspid valves, as estimated angiographically or at autopsy, than those in which the normal three portions of the ventricular cavity were represented.

摘要

室间隔完整的肺动脉闭锁患者预后不佳可能与相关的右心室发育不全有关。对32例患有此病变的新生儿尸检标本和46例心血管造影检查表明,腔室发育不全与右心室壁的大量肥厚有关。这种肥厚足以在三分之一的病例中完全闭塞心室腔的小梁和/或漏斗部;这一观察结果构成了对这些心脏进行修订分类的基础。对3例患有严重肺动脉狭窄的新生儿尸检和14例心血管造影进行了检查。与心室腔正常三个部分均存在的心脏相比,经心血管造影或尸检估计,漏斗部和小梁腔闭塞的心脏具有更厚的壁和更小的三尖瓣。

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