Choi Y H, Seo J W, Choi J Y, Yun Y S, Kim S H, Lee H J
Department of Radiology, Dankook University College of Medicine, Dankook University Hospital, 29 Anseodong Cheonan Choongnam, 330-715, Korea.
Pediatr Cardiol. 1998 Sep-Oct;19(5):381-9. doi: 10.1007/s002469900333.
Pulmonary atresia with intact ventricular septum (PAIVS) is a rare congenital cardiac anomaly that has been classified into two types: one is a more frequent type having dysplasia of tricuspid valve (TV) with a small annulus, underdeveloped right ventricle (RV) with a hypoplastic cavity and a hypertrophic wall; the other type has severe dysplasia of TV and dilatation of RV, right atrium (RA), and right atrioventricular junction with thinning of the RV wall. We performed a morphologic study on 11 autopsied hearts with PAIVS, giving particular emphasis to the variation of morphology of the TV. We could classify these hearts into 3 groups according to the degree of right ventricular development. In the first group of 7 cases (type I), the RVs were underdeveloped. Thick leaflets, restricted valve apparatus with short chordae, and small annuli were characteristics of the TV. In the second group of 3 cases (type II), the RVs showed marked enlargement of the cavity and thinning of the wall. The TV showed redundant, dysplastic, sail-like anterior leaflets, and the downward displacement of septal leaflet and/or posterior leaflet, which are the findings frequently observed in Ebstein's malformation. The RVs were dilated and with partially unguarded tricuspid orifice. The septal leaflet of the TV was dysplastic and, in two cases, the septal leaflet showed chordal structure at the upper surface facing the RA, which is a peculiar finding that has not been described in the literature. The remaining case was a heart with a moderately developed RV (type III). The TV showed mildly dysplastic appearance and we classify this as a separate type, because we could expect the best surgical results in this type. This type had optimal size of RV and the mildest degree of dysplasia of TV. In PAIVS, the morphology of TV correlates well with the type of the right ventricular development.
室间隔完整的肺动脉闭锁(PAIVS)是一种罕见的先天性心脏畸形,已被分为两种类型:一种是较常见的类型,三尖瓣(TV)发育异常,瓣环小,右心室(RV)发育不全,腔室发育不良且壁肥厚;另一种类型则是TV严重发育异常,RV、右心房(RA)及右房室连接处扩张,RV壁变薄。我们对11例PAIVS尸检心脏进行了形态学研究,特别关注TV形态的变化。根据右心室发育程度,我们可将这些心脏分为3组。第一组7例(I型),RV发育不全。TV的特征为瓣叶增厚、瓣膜装置受限伴腱索短、瓣环小。第二组3例(II型),RV腔明显扩大且壁变薄。TV表现为前叶冗长、发育异常呈帆状,隔叶和/或后叶向下移位,这些是埃布斯坦畸形中常见的表现。RV扩张,三尖瓣口部分无瓣环保护。TV隔叶发育异常,2例隔叶在面向RA的上表面显示腱索结构,这是文献中未描述的特殊表现。其余1例心脏RV中度发育(III型)。TV表现为轻度发育异常,我们将其归为单独一种类型,因为预计此型手术效果最佳。此型RV大小适宜,TV发育异常程度最轻。在PAIVS中,TV的形态与右心室发育类型密切相关。