Right aortic arch forming a true vascular ring: a clinical review.


Journal

European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery
ISSN: 1873-734X
Titre abrégé: Eur J Cardiothorac Surg
Pays: Germany
ID NLM: 8804069

Informations de publication

Date de publication:
02 11 2021
Historique:
received: 15 12 2020
revised: 02 03 2021
accepted: 01 04 2021
pubmed: 11 5 2021
medline: 15 12 2021
entrez: 10 5 2021
Statut: ppublish

Résumé

This review aims at presenting and summarizing the current state of literature on the presentation and surgical management of a right-sided aortic arch with a left-sided ligamentum forming a complete vascular ring around the oesophagus and trachea. A systematic database search for appropriate literature was conducted on PubMed/MEDLINE. Articles were considered relevant when providing details on the presentation, diagnosis and surgical treatment of this specific congenital arch anomaly in human beings. Affected patients present with respiratory and/or oesophageal difficulties due to tracheoesophageal compression. Conservative treatment might be reasonable in asymptomatic or mildly symptomatic cases; however, once moderate-to-severe symptoms develop, surgical intervention is definitely indicated. Surgery is commonly performed through a left thoracotomy or median sternotomy and includes the division of the left ductal ligamentum; if a Kommerell's diverticulum is present that is >1.5 times the diameter of the subclavian artery, then concomitant resection of the large diverticulum and translocation of the aberrant left subclavian artery is also conducted. Postoperative morbidity and mortality are low and are rather related to concomitant intracardiac and extracardiac anomalies than to the procedure itself. In a majority of patients, full resolution of symptoms is seen within months to years from the surgery. Nevertheless, there is also a subset of patients who remain with some tracheobronchial narrowing, sometimes even requiring reintervention during follow-up due to persisting or recurring symptoms. Overall, the surgical management of a right aortic arch forming a true vascular ring in infancy, childhood and adulthood seems relatively safe and effective in providing symptomatic relief despite some persistent tracheobronchial and/or oesophageal narrowing in some cases.

Identifiants

pubmed: 33970211
pii: 6273044
doi: 10.1093/ejcts/ezab225
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1014-1021

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.

Auteurs

Daniel Biermann (D)

Department of Cardiothoracic Surgery, Leiden University Medical Center, Leiden, Netherlands.
Surgery for Congenital Heart Disease, University Heart and Vascular Center, Hamburg, Germany.

Theresa Holst (T)

Surgery for Congenital Heart Disease, University Heart and Vascular Center, Hamburg, Germany.

Ida Hüners (I)

Department of Cardiothoracic Surgery, Leiden University Medical Center, Leiden, Netherlands.
Surgery for Congenital Heart Disease, University Heart and Vascular Center, Hamburg, Germany.

Carsten Rickers (C)

Adult Congenital Heart Disease Section, University Heart and Vascular Center, Hamburg, Germany.

Torben Kehl (T)

Department of Pediatric Cardiology, University Heart and Vascular Center, Hamburg, Germany.

André Rüffer (A)

Surgery for Congenital Heart Disease, University Heart and Vascular Center, Hamburg, Germany.

Jörg S Sachweh (JS)

Surgery for Congenital Heart Disease, University Heart and Vascular Center, Hamburg, Germany.

Mark G Hazekamp (MG)

Department of Cardiothoracic Surgery, Leiden University Medical Center, Leiden, Netherlands.

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Classifications MeSH