Cargando…

Tracheoplasty for Congenital Tracheal Stenosis with Bilateral Tracheal Bronchus

Introduction: Congenital tracheal stenosis (CTS) with a bilateral tracheal bronchus (TB) has not been reported as a subtype of CTS. A novel technique to manage CTS in patients with a bilateral TB is described. Case Report: An infant with tetralogy of Fallot underwent repair of cardiac anomaly at age...

Descripción completa

Detalles Bibliográficos
Autores principales: Yamoto, Masaya, Fukumoto, Koji, Urushihara, Naoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Editorial Committee of Annals of Thoracic and Cardiovascular Surgery 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081466/
https://www.ncbi.nlm.nih.gov/pubmed/31996506
http://dx.doi.org/10.5761/atcs.cr.19-00198
_version_ 1784702994732810240
author Yamoto, Masaya
Fukumoto, Koji
Urushihara, Naoto
author_facet Yamoto, Masaya
Fukumoto, Koji
Urushihara, Naoto
author_sort Yamoto, Masaya
collection PubMed
description Introduction: Congenital tracheal stenosis (CTS) with a bilateral tracheal bronchus (TB) has not been reported as a subtype of CTS. A novel technique to manage CTS in patients with a bilateral TB is described. Case Report: An infant with tetralogy of Fallot underwent repair of cardiac anomaly at age 1 month. He experienced numerous cyanosis and episodes of transient respiratory arrest. Chest computed tomography (CT) demonstrated an aberrant bilateral upper lobe bronchus arising directly from the trachea and a stenotic trachea connecting the pseudo- carina to the true carina between the common right lower and left lower bronchus. On bronchoscopy, the diameter of the lumen of the narrowed segment was estimated to be less than 2 mm. Tracheal reconstruction was undertaken when he was 2 years of age. The surgical technique using a modified slide tracheoplasty for the correction of this anomaly are described. After surgery, the patient was extubated and has had no respiratory symptoms. Discussion and Conclusion: The patient had unique anatomic considerations that made reconstruction challenging. Our technique of covering a stenotic section by normal trachea is a modification of the slide tracheoplasty technique and is useful for CTS with a unilateral and a bilateral TB.
format Online
Article
Text
id pubmed-9081466
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The Editorial Committee of Annals of Thoracic and Cardiovascular Surgery
record_format MEDLINE/PubMed
spelling pubmed-90814662022-05-21 Tracheoplasty for Congenital Tracheal Stenosis with Bilateral Tracheal Bronchus Yamoto, Masaya Fukumoto, Koji Urushihara, Naoto Ann Thorac Cardiovasc Surg Case Report Introduction: Congenital tracheal stenosis (CTS) with a bilateral tracheal bronchus (TB) has not been reported as a subtype of CTS. A novel technique to manage CTS in patients with a bilateral TB is described. Case Report: An infant with tetralogy of Fallot underwent repair of cardiac anomaly at age 1 month. He experienced numerous cyanosis and episodes of transient respiratory arrest. Chest computed tomography (CT) demonstrated an aberrant bilateral upper lobe bronchus arising directly from the trachea and a stenotic trachea connecting the pseudo- carina to the true carina between the common right lower and left lower bronchus. On bronchoscopy, the diameter of the lumen of the narrowed segment was estimated to be less than 2 mm. Tracheal reconstruction was undertaken when he was 2 years of age. The surgical technique using a modified slide tracheoplasty for the correction of this anomaly are described. After surgery, the patient was extubated and has had no respiratory symptoms. Discussion and Conclusion: The patient had unique anatomic considerations that made reconstruction challenging. Our technique of covering a stenotic section by normal trachea is a modification of the slide tracheoplasty technique and is useful for CTS with a unilateral and a bilateral TB. The Editorial Committee of Annals of Thoracic and Cardiovascular Surgery 2020-01-29 2022 /pmc/articles/PMC9081466/ /pubmed/31996506 http://dx.doi.org/10.5761/atcs.cr.19-00198 Text en ©2022 Annals of Thoracic and Cardiovascular Surgery https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NonDerivatives International License (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Case Report
Yamoto, Masaya
Fukumoto, Koji
Urushihara, Naoto
Tracheoplasty for Congenital Tracheal Stenosis with Bilateral Tracheal Bronchus
title Tracheoplasty for Congenital Tracheal Stenosis with Bilateral Tracheal Bronchus
title_full Tracheoplasty for Congenital Tracheal Stenosis with Bilateral Tracheal Bronchus
title_fullStr Tracheoplasty for Congenital Tracheal Stenosis with Bilateral Tracheal Bronchus
title_full_unstemmed Tracheoplasty for Congenital Tracheal Stenosis with Bilateral Tracheal Bronchus
title_short Tracheoplasty for Congenital Tracheal Stenosis with Bilateral Tracheal Bronchus
title_sort tracheoplasty for congenital tracheal stenosis with bilateral tracheal bronchus
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081466/
https://www.ncbi.nlm.nih.gov/pubmed/31996506
http://dx.doi.org/10.5761/atcs.cr.19-00198
work_keys_str_mv AT yamotomasaya tracheoplastyforcongenitaltrachealstenosiswithbilateraltrachealbronchus
AT fukumotokoji tracheoplastyforcongenitaltrachealstenosiswithbilateraltrachealbronchus
AT urushiharanaoto tracheoplastyforcongenitaltrachealstenosiswithbilateraltrachealbronchus