| Literature DB >> 32315647 |
Nobuyasu Kato1, Tsuyoshi Tachibana2, Hidetsugu Asai2, Noriyoshi Ebuoka3, Yasushige Shingu4, Tomonori Ooka4, Hiroki Kato5, Satoru Wakasa4.
Abstract
Persistent fifth aortic arch (AA) is a rare anomaly in congenital heart disease, which is often associated with aortic obstructive diseases. We report a 7-month-old infant diagnosed with persistent fifth AA with left ventricular dysfunction along with left bronchial malacia due to compression from their own heart. Surgical repair was performed, including AA reconstruction using the fifth AA as an in situ flap to enlarge the fourth AA with end-to-end anastomosis, and external stenting for the left bronchial malacia. Postoperative courses were uneventful. On computed tomography, a reconstructed AA without obstruction and an expanded left bronchus were seen.Entities:
Mesh:
Year: 2020 PMID: 32315647 DOI: 10.1016/j.athoracsur.2020.03.039
Source DB: PubMed Journal: Ann Thorac Surg ISSN: 0003-4975 Impact factor: 4.330