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An Unusual Cause of Spontaneous Pneumomediastinum: The Mounier-Kuhn Syndrome

Mounier-Kuhn syndrome is a rare clinical and radiologic condition. It is characterized by tracheal and bronchial dilation. Diagnosis is made by computed tomography and bronchoscopy. An 81-year-old man presenting with an acute chest pain was referred to the pulmonology department. His chest computed...

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Autores principales: Naciri, Salim, Zahraoui, Rachida, Soualhi, Mouna, Bourkadi, Jamal-Eddine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644234/
https://www.ncbi.nlm.nih.gov/pubmed/31360573
http://dx.doi.org/10.1155/2019/5359309
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author Naciri, Salim
Zahraoui, Rachida
Soualhi, Mouna
Bourkadi, Jamal-Eddine
author_facet Naciri, Salim
Zahraoui, Rachida
Soualhi, Mouna
Bourkadi, Jamal-Eddine
author_sort Naciri, Salim
collection PubMed
description Mounier-Kuhn syndrome is a rare clinical and radiologic condition. It is characterized by tracheal and bronchial dilation. Diagnosis is made by computed tomography and bronchoscopy. An 81-year-old man presenting with an acute chest pain was referred to the pulmonology department. His chest computed tomographic scan showed a tracheobronchomegaly with an increase in the diameter of both the trachea and right and left main bronchi, associated with pneumomediastinum and fibrosis. Fiberoptic bronchoscopy revealed enlarged trachea and both main bronchi. These findings are consistent with a diagnosis of Mounier-Kuhn syndrome. Besides considering this long-neglected “orphan disease” when diagnosing spontaneous pneumomediastinum, clinicians should also be aware of an underlying Mounier-Kuhn syndrome in patients with recurrent respiratory infections, in order to avoid complications associated with the disease.
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spelling pubmed-66442342019-07-29 An Unusual Cause of Spontaneous Pneumomediastinum: The Mounier-Kuhn Syndrome Naciri, Salim Zahraoui, Rachida Soualhi, Mouna Bourkadi, Jamal-Eddine Case Rep Pulmonol Case Report Mounier-Kuhn syndrome is a rare clinical and radiologic condition. It is characterized by tracheal and bronchial dilation. Diagnosis is made by computed tomography and bronchoscopy. An 81-year-old man presenting with an acute chest pain was referred to the pulmonology department. His chest computed tomographic scan showed a tracheobronchomegaly with an increase in the diameter of both the trachea and right and left main bronchi, associated with pneumomediastinum and fibrosis. Fiberoptic bronchoscopy revealed enlarged trachea and both main bronchi. These findings are consistent with a diagnosis of Mounier-Kuhn syndrome. Besides considering this long-neglected “orphan disease” when diagnosing spontaneous pneumomediastinum, clinicians should also be aware of an underlying Mounier-Kuhn syndrome in patients with recurrent respiratory infections, in order to avoid complications associated with the disease. Hindawi 2019-07-08 /pmc/articles/PMC6644234/ /pubmed/31360573 http://dx.doi.org/10.1155/2019/5359309 Text en Copyright © 2019 Salim Naciri et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Naciri, Salim
Zahraoui, Rachida
Soualhi, Mouna
Bourkadi, Jamal-Eddine
An Unusual Cause of Spontaneous Pneumomediastinum: The Mounier-Kuhn Syndrome
title An Unusual Cause of Spontaneous Pneumomediastinum: The Mounier-Kuhn Syndrome
title_full An Unusual Cause of Spontaneous Pneumomediastinum: The Mounier-Kuhn Syndrome
title_fullStr An Unusual Cause of Spontaneous Pneumomediastinum: The Mounier-Kuhn Syndrome
title_full_unstemmed An Unusual Cause of Spontaneous Pneumomediastinum: The Mounier-Kuhn Syndrome
title_short An Unusual Cause of Spontaneous Pneumomediastinum: The Mounier-Kuhn Syndrome
title_sort unusual cause of spontaneous pneumomediastinum: the mounier-kuhn syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644234/
https://www.ncbi.nlm.nih.gov/pubmed/31360573
http://dx.doi.org/10.1155/2019/5359309
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