Fukuda T, Suzuki T, Sato M, Morikawa M
Department of Cardiovascular Surgery, Tokyo Metropolitan Children's Hospital, 1-3-1 Umezono, Kiyose, Tokyo 204-8567, Japan.
Pediatr Cardiol. 1999 May-Jun;20(3):232-5. doi: 10.1007/s002469900451.
A case child with complete atrioventricular septal defect (AVSD) and Ebstein's anomaly underwent surgical treatment at 3 months of age. She died on the third postoperative day. Postmortem examination showed complete AVSD, downward displacement of the right atrioventricular valve, left ventricular outflow tract obstruction, and hypertensive pulmonary vascular disease. Association of complete AVSD and Ebstein's anomaly is a rare cardiac anomaly for which no attempt at surgical repair has previously been made. This report deals with our experience and also with the morphological features of this anomaly.
一名患有完全性房室间隔缺损(AVSD)和埃布斯坦畸形的患儿在3个月大时接受了手术治疗。她在术后第三天死亡。尸检显示完全性AVSD、右房室瓣向下移位、左心室流出道梗阻和高血压性肺血管疾病。完全性AVSD与埃布斯坦畸形的关联是一种罕见的心脏畸形,此前尚未有人尝试进行手术修复。本报告阐述了我们的经验以及这种畸形的形态学特征。