Matsuoka Y, Yamasaki S, Nishiguchi T, Okishima T, Ando M
Department of Pediatrics, Miyazaki Medical College, Japan.
Pediatr Cardiol. 1994 May-Jun;15(3):146-50. doi: 10.1007/BF00796328.
Isolated ventricular inversion with concomitant atresia of the left-sided (tricuspid) atrioventricular valve has previously been reported in the English literature in only two patients, and they died during early infancy. We describe the clinical, two-dimensional echocardiographic and angiocardiographic features in a 10-year-old boy with these rare cardiac anomalies in association with unroofed coronary sinus, which compensated for the restrictive atrial septal defect. This is the first published report of this combination of cardiac anomalies.
孤立性心室反位合并左侧(三尖瓣)房室瓣闭锁,此前英文文献仅报道过两例患者,且他们均在婴儿早期死亡。我们描述了一名10岁男孩的临床、二维超声心动图和心血管造影特征,该男孩患有这些罕见的心脏异常,并伴有未闭冠状静脉窦,后者代偿了限制性房间隔缺损。这是首次发表的关于这种心脏异常组合的报告。