Fuchigami Tai, Nishioka Masahiko, Akashige Toru, Nabeshima Taisuke, Nagata Nobuhiro
1 Department of Pediatric Cardiovascular Surgery, Okinawa Prefectural Nanbu Medical Center & Children's Medical Center, Haebaru-cho, Okinawa, Japan.
2 Department of Pediatric Cardiology, Okinawa Prefectural Nanbu Medical Center & Children's Medical Center, Haebaru-cho, Okinawa, Japan.
Asian Cardiovasc Thorac Ann. 2017 Jan;25(1):62-64. doi: 10.1177/0218492315622102. Epub 2016 Jul 11.
The association of total anomalous pulmonary venous connection with ventricular septal defect and aortic coarctation is rare. A premature neonate weighing 1350 g was diagnosed with infracardiac total anomalous pulmonary venous connection, aortic coarctation, and a perimembranous ventricular septal defect. On postnatal day 23, we performed emergency extended aortic arch anastomosis under total circulatory arrest, pulmonary venous connection repair using a primary sutureless technique, and patch closure of the atrial septal and perimembranous ventricular septal defects. The patient was discharged without complications. Postoperative echocardiography showed no residual coarctation or pulmonary venous obstruction and revealed small muscular ventricular septal defects.
完全性肺静脉异位连接合并室间隔缺损和主动脉缩窄的情况较为罕见。一名体重1350克的早产新生儿被诊断为心内型完全性肺静脉异位连接、主动脉缩窄和膜周部室间隔缺损。出生后第23天,我们在全循环停搏下进行了紧急扩大主动脉弓吻合术,采用原发性无缝合技术修复肺静脉连接,并对房间隔和膜周部室间隔缺损进行补片修补。患者出院时无并发症。术后超声心动图显示无残余缩窄或肺静脉梗阻,并发现有小的肌部室间隔缺损。