Case Report
Copyright ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Cardiol. Feb 26, 2017; 9(2): 191-195
Published online Feb 26, 2017. doi: 10.4330/wjc.v9.i2.191
Dysphagia after arteria lusoria dextra surgery: Anatomical considerations before redo-surgery
Judith Mayer, Natascha van der Werf-Grohmann, Johannes Kroll, Ute Spiekerkoetter, Brigitte Stiller, Jochen Grohmann
Judith Mayer, Natascha van der Werf-Grohmann, Ute Spiekerkoetter, Department of Pediatrics and Adolescent Medicine, Freiburg University, 79106 Freiburg, Germany
Johannes Kroll, Department of Cardiovascular Surgery, Heart Center, Freiburg University, 79106 Freiburg, Germany
Brigitte Stiller, Jochen Grohmann, Department of Congenital Heart Disease and Pediatric Cardiology, Heart Center, Freiburg University, 79106 Freiburg, Germany
Author contributions: Mayer J drafted the initial and further case report; Kroll J as experienced pediatric cardiovascular surgeon performed both operations and contributed important, detailed information for the surgical and anatomical discussion; Grohmann J was one of the leading cardiologists in charge during the entire duration of treatment and played an important role in developing and reviewing the final manuscript; all authors were involved in the patient management as an interdisciplinary team, critically reviewed the manuscript and approved the final manuscript as submitted.
Institutional review board statement: None.
Informed consent statement: All involved persons, or their legal guardians, provided informed written consent prior to submitting the case report.
Conflict-of-interest statement: The authors have no conflict of interest to declare.
Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Correspondence to: Jochen Grohmann, MD, Department of Congenital Heart Disease and Pediatric Cardiology, Heart Center, Freiburg University, Mathildenstrasse 1, 79106 Freiburg, Germany. jochen.grohmann@universitaets-herzzentrum.de
Telephone: +49-761-27043000 Fax: +49-761-27044680
Received: October 13, 2016
Peer-review started: October 17, 2016
First decision: November 14, 2016
Revised: November 28, 2016
Accepted: December 13, 2016
Article in press: December 15, 2016
Published online: February 26, 2017
Processing time: 133 Days and 9.7 Hours
Core Tip

Core tip: We present a pediatric case of dysphagia caused by the common congenital root anomaly of an aberrant right subclavian artery. However, persisting symptoms after primary treatment via right-sided thoracotomy required redo-surgery via left-sided thoracotomy with transection of a persisting ligamentum arteriosum and shortening of the remaining lusorian arteries’ stump. Based on this experience, we want to emphasize the potential co-existence of a compressing ligamentum arteriosum even in patients with left aortic arch.