Literature DB >> 32315647

Persistent Fifth Aortic Arch With Left Ventricular Dysfunction and Left Bronchial Obstruction.

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.
Copyright © 2020 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

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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


  1 in total

1.  Persistent fifth aortic arch: a single-center experience, case series.

Authors:  Yuanyuan Liu; Hui Zhang; Jun Ren; Aimei Cao; Jinghui Guo; Bo Liu; Min Bao; Chunhua Zheng
Journal:  Transl Pediatr       Date:  2021-06
  1 in total

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