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Esophageal Trachea, a Unique Foregut Malformation Requiring Multistage Surgical Reconstruction: Case Report

Abnormal connections between the esophagus and low respiratory tract can result from embryological defects in foregut development. Beyond well-known malformations, including tracheo-esophageal fistula and laryngo-tracheo-esophageal cleft, rarer anomalies have also been reported, including communicat...

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Autores principales: Tambucci, Roberto, Wautelet, Océane, Haenecour, Astrid, François, Geneviève, Goubau, Christophe, Scheers, Isabelle, Halut, Marin, Menten, Renaud, Schmitz, Sandra, de Toeuf, Caroline, Pirotte, Thierry, D'hondt, Beelke, Reding, Raymond, Poncelet, Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714922/
https://www.ncbi.nlm.nih.gov/pubmed/33330293
http://dx.doi.org/10.3389/fped.2020.605143
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author Tambucci, Roberto
Wautelet, Océane
Haenecour, Astrid
François, Geneviève
Goubau, Christophe
Scheers, Isabelle
Halut, Marin
Menten, Renaud
Schmitz, Sandra
de Toeuf, Caroline
Pirotte, Thierry
D'hondt, Beelke
Reding, Raymond
Poncelet, Alain
author_facet Tambucci, Roberto
Wautelet, Océane
Haenecour, Astrid
François, Geneviève
Goubau, Christophe
Scheers, Isabelle
Halut, Marin
Menten, Renaud
Schmitz, Sandra
de Toeuf, Caroline
Pirotte, Thierry
D'hondt, Beelke
Reding, Raymond
Poncelet, Alain
author_sort Tambucci, Roberto
collection PubMed
description Abnormal connections between the esophagus and low respiratory tract can result from embryological defects in foregut development. Beyond well-known malformations, including tracheo-esophageal fistula and laryngo-tracheo-esophageal cleft, rarer anomalies have also been reported, including communicating bronchopulmonary foregut malformations and tracheal atresia. Herein, we describe a case of what we have called “esophageal trachea,” which, to our knowledge, has yet to be reported. A full-term neonate was born in our institution presenting with a foregut malformation involving both the middle esophagus and the distal trachea, which were found to be longitudinally merged into a common segment, 3 cm in length, located just above the carina and consisted of esophageal tissue without cartilaginous rings. At birth, the esophagus and trachea were surgically separated via right thoracotomy, the common segment kept on the tracheal side only, creating a residual long-gap esophageal atresia. The resulting severe tracheomalacia was treated via simultaneous posterior splinting of such diseased segment using an autologous pericardium patch, as well as by anterior aortopexy. Terminal esophagostomy and gastrostomy were created at that stage due to the long distance between esophageal segments. Between ages 18 and 24 months, the patient underwent native esophageal reconstruction using a multistage traction-and-growth surgical strategy that combined Kimura extra-thoracic esophageal elongations at the upper esophagus and Foker external traction at the distal esophagus. Ten months after esophageal reconstruction, prolonged, refractory, and severe tracheomalacia was further treated via anterior external stenting using a semitubular ringed Gore-Tex® prosthesis, through simultaneous median sternotomy and tracheoscopy. Currently, 2 years after the last surgery, respiratory stabilization, and full oral feeding were stably achieved. Multidisciplinary management was crucial for assuring lifesaving procedures, correctly assessing anatomy, and planning for multiple sequential surgical approaches that aimed to restore long-term respiratory and digestive functions.
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spelling pubmed-77149222020-12-15 Esophageal Trachea, a Unique Foregut Malformation Requiring Multistage Surgical Reconstruction: Case Report Tambucci, Roberto Wautelet, Océane Haenecour, Astrid François, Geneviève Goubau, Christophe Scheers, Isabelle Halut, Marin Menten, Renaud Schmitz, Sandra de Toeuf, Caroline Pirotte, Thierry D'hondt, Beelke Reding, Raymond Poncelet, Alain Front Pediatr Pediatrics Abnormal connections between the esophagus and low respiratory tract can result from embryological defects in foregut development. Beyond well-known malformations, including tracheo-esophageal fistula and laryngo-tracheo-esophageal cleft, rarer anomalies have also been reported, including communicating bronchopulmonary foregut malformations and tracheal atresia. Herein, we describe a case of what we have called “esophageal trachea,” which, to our knowledge, has yet to be reported. A full-term neonate was born in our institution presenting with a foregut malformation involving both the middle esophagus and the distal trachea, which were found to be longitudinally merged into a common segment, 3 cm in length, located just above the carina and consisted of esophageal tissue without cartilaginous rings. At birth, the esophagus and trachea were surgically separated via right thoracotomy, the common segment kept on the tracheal side only, creating a residual long-gap esophageal atresia. The resulting severe tracheomalacia was treated via simultaneous posterior splinting of such diseased segment using an autologous pericardium patch, as well as by anterior aortopexy. Terminal esophagostomy and gastrostomy were created at that stage due to the long distance between esophageal segments. Between ages 18 and 24 months, the patient underwent native esophageal reconstruction using a multistage traction-and-growth surgical strategy that combined Kimura extra-thoracic esophageal elongations at the upper esophagus and Foker external traction at the distal esophagus. Ten months after esophageal reconstruction, prolonged, refractory, and severe tracheomalacia was further treated via anterior external stenting using a semitubular ringed Gore-Tex® prosthesis, through simultaneous median sternotomy and tracheoscopy. Currently, 2 years after the last surgery, respiratory stabilization, and full oral feeding were stably achieved. Multidisciplinary management was crucial for assuring lifesaving procedures, correctly assessing anatomy, and planning for multiple sequential surgical approaches that aimed to restore long-term respiratory and digestive functions. Frontiers Media S.A. 2020-11-20 /pmc/articles/PMC7714922/ /pubmed/33330293 http://dx.doi.org/10.3389/fped.2020.605143 Text en Copyright © 2020 Tambucci, Wautelet, Haenecour, François, Goubau, Scheers, Halut, Menten, Schmitz, de Toeuf, Pirotte, D'hondt, Reding and Poncelet. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Tambucci, Roberto
Wautelet, Océane
Haenecour, Astrid
François, Geneviève
Goubau, Christophe
Scheers, Isabelle
Halut, Marin
Menten, Renaud
Schmitz, Sandra
de Toeuf, Caroline
Pirotte, Thierry
D'hondt, Beelke
Reding, Raymond
Poncelet, Alain
Esophageal Trachea, a Unique Foregut Malformation Requiring Multistage Surgical Reconstruction: Case Report
title Esophageal Trachea, a Unique Foregut Malformation Requiring Multistage Surgical Reconstruction: Case Report
title_full Esophageal Trachea, a Unique Foregut Malformation Requiring Multistage Surgical Reconstruction: Case Report
title_fullStr Esophageal Trachea, a Unique Foregut Malformation Requiring Multistage Surgical Reconstruction: Case Report
title_full_unstemmed Esophageal Trachea, a Unique Foregut Malformation Requiring Multistage Surgical Reconstruction: Case Report
title_short Esophageal Trachea, a Unique Foregut Malformation Requiring Multistage Surgical Reconstruction: Case Report
title_sort esophageal trachea, a unique foregut malformation requiring multistage surgical reconstruction: case report
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714922/
https://www.ncbi.nlm.nih.gov/pubmed/33330293
http://dx.doi.org/10.3389/fped.2020.605143
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