Cargando…

Tracheocele: A Rare Entity

INTRODUCTION: Tracheocele or tracheal diverticulum is an uncommon benign entity that can be congenital or acquired. It is usually diagnosed incidentally on cervicothoracic imaging. Our aim is to describe the etiopathogenic, clinical and paraclinical features of the tracheocele as well as its therape...

Descripción completa

Detalles Bibliográficos
Autores principales: Kallel, Souha, Chaabouni, Mohamed Amin, Thabet, Wadii, Mnejja, Malek, Ben Mahfoudh, Khaireddine, Charfeddine, Ilhem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392997/
https://www.ncbi.nlm.nih.gov/pubmed/36035650
http://dx.doi.org/10.22038/IJORL.2022.53313.2815
_version_ 1784771176342487040
author Kallel, Souha
Chaabouni, Mohamed Amin
Thabet, Wadii
Mnejja, Malek
Ben Mahfoudh, Khaireddine
Charfeddine, Ilhem
author_facet Kallel, Souha
Chaabouni, Mohamed Amin
Thabet, Wadii
Mnejja, Malek
Ben Mahfoudh, Khaireddine
Charfeddine, Ilhem
author_sort Kallel, Souha
collection PubMed
description INTRODUCTION: Tracheocele or tracheal diverticulum is an uncommon benign entity that can be congenital or acquired. It is usually diagnosed incidentally on cervicothoracic imaging. Our aim is to describe the etiopathogenic, clinical and paraclinical features of the tracheocele as well as its therapeutic modalities. CASE REPORT: We report 2 cases of asymptomatic congenital tracheocele occurred in a boy and a woman, incidentally found on cervical CT scan done for accidental ingestion of chicken bone and infected thyroid hematocele respectively. The tracheocele, in our 2 cases, was probably congenital: no risk factors were noted and the opening of the tracheocele was narrow. The tracheocele was located in the right posterolateral tracheal wall in the 2 cases. It communicated with the tracheal lumen in one case. The female patient underwent a right lobectomy and resection of the tracheocele. For the boy, our attitude was conservative. The evolution was uneventful in the 2 cases. CONCLUSIONS: The presence or absence of risk factors, CT scan, bronchoscopy and histologic exam may distinguish between congenital and acquired forms. Asymptomatic patients are managed conservatively. Surgical resection is the treatment of choice for symptomatic patients.
format Online
Article
Text
id pubmed-9392997
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Mashhad University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-93929972022-08-26 Tracheocele: A Rare Entity Kallel, Souha Chaabouni, Mohamed Amin Thabet, Wadii Mnejja, Malek Ben Mahfoudh, Khaireddine Charfeddine, Ilhem Iran J Otorhinolaryngol Case Report INTRODUCTION: Tracheocele or tracheal diverticulum is an uncommon benign entity that can be congenital or acquired. It is usually diagnosed incidentally on cervicothoracic imaging. Our aim is to describe the etiopathogenic, clinical and paraclinical features of the tracheocele as well as its therapeutic modalities. CASE REPORT: We report 2 cases of asymptomatic congenital tracheocele occurred in a boy and a woman, incidentally found on cervical CT scan done for accidental ingestion of chicken bone and infected thyroid hematocele respectively. The tracheocele, in our 2 cases, was probably congenital: no risk factors were noted and the opening of the tracheocele was narrow. The tracheocele was located in the right posterolateral tracheal wall in the 2 cases. It communicated with the tracheal lumen in one case. The female patient underwent a right lobectomy and resection of the tracheocele. For the boy, our attitude was conservative. The evolution was uneventful in the 2 cases. CONCLUSIONS: The presence or absence of risk factors, CT scan, bronchoscopy and histologic exam may distinguish between congenital and acquired forms. Asymptomatic patients are managed conservatively. Surgical resection is the treatment of choice for symptomatic patients. Mashhad University of Medical Sciences 2022-07 /pmc/articles/PMC9392997/ /pubmed/36035650 http://dx.doi.org/10.22038/IJORL.2022.53313.2815 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kallel, Souha
Chaabouni, Mohamed Amin
Thabet, Wadii
Mnejja, Malek
Ben Mahfoudh, Khaireddine
Charfeddine, Ilhem
Tracheocele: A Rare Entity
title Tracheocele: A Rare Entity
title_full Tracheocele: A Rare Entity
title_fullStr Tracheocele: A Rare Entity
title_full_unstemmed Tracheocele: A Rare Entity
title_short Tracheocele: A Rare Entity
title_sort tracheocele: a rare entity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392997/
https://www.ncbi.nlm.nih.gov/pubmed/36035650
http://dx.doi.org/10.22038/IJORL.2022.53313.2815
work_keys_str_mv AT kallelsouha tracheocelearareentity
AT chaabounimohamedamin tracheocelearareentity
AT thabetwadii tracheocelearareentity
AT mnejjamalek tracheocelearareentity
AT benmahfoudhkhaireddine tracheocelearareentity
AT charfeddineilhem tracheocelearareentity