Wetzel Ulrike, Scholtz Werner, Bogunovic Nikola, Körfer Jan, Haas Nikolaus A, Blanz Ute, Körfer Reiner, Kececioglu Deniz, Horstkotte Dieter
Department of Cardiology, Heart and Diabetes Center North Rhine-Westphalia, Ruhr University Bochum, Bad Oeynhausen, Germany.
Congenit Heart Dis. 2010 Sep-Oct;5(5):470-5. doi: 10.1111/j.1747-0803.2009.00372.x.
Total anomalous pulmonary venous connection is a rare variant of cyanotic congenital heart disease and usually requires surgical correction within the first few months of life. We report midterm results of a 63-year-old male with intracardiac total anomalous venous return into the coronary sinus who presented with congestive predominantly right heart failure and underwent corrective surgery with unroofing of the coronary sinus and patch closure of the secundum atrial septal defect.
完全性肺静脉异位连接是一种罕见的青紫型先天性心脏病变异，通常需要在出生后的头几个月内进行手术矫正。我们报告了一名63岁男性患者的中期结果，该患者心脏内完全性肺静脉异位引流至冠状窦，表现为以右心为主的充血性心力衰竭，并接受了冠状窦开窗及继发孔房间隔缺损补片修补的矫正手术。
