Journal of Pediatric Cardiology and Cardiac Surgery

Online ISSN: 2433-1783 Print ISSN: 2433-2720
Japanese Society of Pediatric Cardiology and Cardiac Surgery
Japanese Society of Pediatric Cardiology and Cardiac Surgery Academy Center, 358-5 Yamabuki-cho, Shinju-ku, Tokyo 162-0801, Japan
Journal of Pediatric Cardiology and Cardiac Surgery 6(2): 66-69 (2022)
doi:10.24509/jpccs.21-032

Case ReportCase Report

Anomalous Origin of the Right Pulmonary Artery from the Ascending Aorta with Aortic Coarctation

1Department of Cardiovascular Surgery, JCHO Kyushu Hospital ◇ Fukuoka, Japan

2Department of Pediatric Cardiology, JCHO Kyushu Hospital ◇ Fukuoka, Japan

受付日:2021年12月22日Received: December 22, 2021
受理日:2022年2月15日Accepted: February 15, 2022
発行日:2022年7月1日Published: July 1, 2022
HTMLPDFEPUB3

Two neonates were treated for a combination of a distal type of anomalous origin of the right pulmonary artery from the ascending aorta and aortic coarctation. Aortic arch reconstruction was performed using an extended aortic arch anastomosis in both cases. In the first case, the right pulmonary artery was reconstructed by a direct anastomosis behind the ascending aorta. Early reoperation for graft interposition was required to treat stenosis at the proximal right pulmonary artery due to a residual ductal tissue there. In the second case, such ductal tissues were sufficiently resected at the initial repair, and the right pulmonary artery was reconstructed using an artificial graft anterior to the ascending aorta. As aortic arch reconstruction for aortic coarctation reduces the space posterior to the ascending aorta, an appropriate route should be considered sensibly for the right pulmonary artery to be reconstructed.

Key words: anomalous origin of the right pulmonary artery; cardiac defect; coarctation of the aorta; persistent fifth aortic arch

This page was created on 2022-06-02T14:04:49.508+09:00
This page was last modified on 2022-08-03T17:00:35.000+09:00


このサイトは(株)国際文献社によって運用されています。