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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Mashhad University of Medical Sciences
2022
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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 |
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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 |
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