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Successful management of congenital bronchial web in an adolescent using bronchoscopic ablation: A case report and review of literature
Airway webs are abnormal fibrous membranes in the airway lumen that rarely occur but can lead to serious or even life-threatening symptoms because of critical airway obstruction. Airway webs can be acquired or congenital. Acquired webs are likely to be secondary to trauma, infections, or neoplasm. C...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763669/ https://www.ncbi.nlm.nih.gov/pubmed/36561962 http://dx.doi.org/10.1016/j.rmcr.2022.101786 |
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author | Hamad, Sara G. Abushahin, Ahmed Abdulsattar, Hisham Waqas, Kashif Abu-Hasan, Mutasim |
author_facet | Hamad, Sara G. Abushahin, Ahmed Abdulsattar, Hisham Waqas, Kashif Abu-Hasan, Mutasim |
author_sort | Hamad, Sara G. |
collection | PubMed |
description | Airway webs are abnormal fibrous membranes in the airway lumen that rarely occur but can lead to serious or even life-threatening symptoms because of critical airway obstruction. Airway webs can be acquired or congenital. Acquired webs are likely to be secondary to trauma, infections, or neoplasm. Congenital laryngeal, subglottic and tracheal webs present early in infancy or childhood and are more common than congenital bronchial webs. To our knowledge, there are a few reports on the bronchial web in the literature, and the true incidence of these lesions is unknown as many probably go undetected across the lifespan. We here report a case of a congenital bronchial web and provide a review of the literature of all reported bronchial webs. Our patient is a teenage boy who was diagnosed with a congenital bronchial web obstructing the right main-stem bronchus (RMB) and causing right lung hypoplasia and persistent right middle and right lower lobe collapse. The web was treated successfully using endoscopic ablation by argon plasma coagulation and balloon dilatation. Treatment resulted in remarkable relief of right main stem obstruction and significant improvement in right lung collapse as well as clinical, spirometric, and radiological findings. Due to the rarity of bronchial web, the clinical knowledge and the bronchoscopic interventional strategies demonstrated of this report make it relevant. Furthermore, it emphasizes that early diagnosis and management lead to favorable clinical outcomes. |
format | Online Article Text |
id | pubmed-9763669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97636692022-12-21 Successful management of congenital bronchial web in an adolescent using bronchoscopic ablation: A case report and review of literature Hamad, Sara G. Abushahin, Ahmed Abdulsattar, Hisham Waqas, Kashif Abu-Hasan, Mutasim Respir Med Case Rep Case Report Airway webs are abnormal fibrous membranes in the airway lumen that rarely occur but can lead to serious or even life-threatening symptoms because of critical airway obstruction. Airway webs can be acquired or congenital. Acquired webs are likely to be secondary to trauma, infections, or neoplasm. Congenital laryngeal, subglottic and tracheal webs present early in infancy or childhood and are more common than congenital bronchial webs. To our knowledge, there are a few reports on the bronchial web in the literature, and the true incidence of these lesions is unknown as many probably go undetected across the lifespan. We here report a case of a congenital bronchial web and provide a review of the literature of all reported bronchial webs. Our patient is a teenage boy who was diagnosed with a congenital bronchial web obstructing the right main-stem bronchus (RMB) and causing right lung hypoplasia and persistent right middle and right lower lobe collapse. The web was treated successfully using endoscopic ablation by argon plasma coagulation and balloon dilatation. Treatment resulted in remarkable relief of right main stem obstruction and significant improvement in right lung collapse as well as clinical, spirometric, and radiological findings. Due to the rarity of bronchial web, the clinical knowledge and the bronchoscopic interventional strategies demonstrated of this report make it relevant. Furthermore, it emphasizes that early diagnosis and management lead to favorable clinical outcomes. Elsevier 2022-12-09 /pmc/articles/PMC9763669/ /pubmed/36561962 http://dx.doi.org/10.1016/j.rmcr.2022.101786 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Hamad, Sara G. Abushahin, Ahmed Abdulsattar, Hisham Waqas, Kashif Abu-Hasan, Mutasim Successful management of congenital bronchial web in an adolescent using bronchoscopic ablation: A case report and review of literature |
title | Successful management of congenital bronchial web in an adolescent using bronchoscopic ablation: A case report and review of literature |
title_full | Successful management of congenital bronchial web in an adolescent using bronchoscopic ablation: A case report and review of literature |
title_fullStr | Successful management of congenital bronchial web in an adolescent using bronchoscopic ablation: A case report and review of literature |
title_full_unstemmed | Successful management of congenital bronchial web in an adolescent using bronchoscopic ablation: A case report and review of literature |
title_short | Successful management of congenital bronchial web in an adolescent using bronchoscopic ablation: A case report and review of literature |
title_sort | successful management of congenital bronchial web in an adolescent using bronchoscopic ablation: a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763669/ https://www.ncbi.nlm.nih.gov/pubmed/36561962 http://dx.doi.org/10.1016/j.rmcr.2022.101786 |
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