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Chronic Pulmonary Aspergillosis Complicating Bronchial Atresia

Bronchial atresia is a rare pulmonary developmental anomaly characterized by the presence of a focal obliteration of a segmental or lobar bronchial lumen. The lung distal to the atretic bronchus is typically emphysematous along with the presence of mucus filled ectatic bronchi (mucoceles). BA is usu...

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Autores principales: Al-Qadi, Mazen O., Reddy, Dereddi Raja S., Larsen, Brandon T., Iyer, Vivek N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283422/
https://www.ncbi.nlm.nih.gov/pubmed/25587281
http://dx.doi.org/10.1155/2014/208963
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author Al-Qadi, Mazen O.
Reddy, Dereddi Raja S.
Larsen, Brandon T.
Iyer, Vivek N.
author_facet Al-Qadi, Mazen O.
Reddy, Dereddi Raja S.
Larsen, Brandon T.
Iyer, Vivek N.
author_sort Al-Qadi, Mazen O.
collection PubMed
description Bronchial atresia is a rare pulmonary developmental anomaly characterized by the presence of a focal obliteration of a segmental or lobar bronchial lumen. The lung distal to the atretic bronchus is typically emphysematous along with the presence of mucus filled ectatic bronchi (mucoceles). BA is usually asymptomatic but pulmonary infections can rarely develop in the emphysematous lung distal to the atretic bronchus. We present a unique case of chronic pulmonary aspergillosis (CPA) in a patient with BA with no evidence of immune dysfunction. The patient was treated initially with voriconazole and subsequently underwent surgical excision of the involved area. On follow-up, she has done extremely well with no evidence for recurrence. In summary, we describe the first case of chronic pulmonary aspergillosis in an immunocompetent patient with bronchial atresia.
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spelling pubmed-42834222015-01-13 Chronic Pulmonary Aspergillosis Complicating Bronchial Atresia Al-Qadi, Mazen O. Reddy, Dereddi Raja S. Larsen, Brandon T. Iyer, Vivek N. Case Rep Med Case Report Bronchial atresia is a rare pulmonary developmental anomaly characterized by the presence of a focal obliteration of a segmental or lobar bronchial lumen. The lung distal to the atretic bronchus is typically emphysematous along with the presence of mucus filled ectatic bronchi (mucoceles). BA is usually asymptomatic but pulmonary infections can rarely develop in the emphysematous lung distal to the atretic bronchus. We present a unique case of chronic pulmonary aspergillosis (CPA) in a patient with BA with no evidence of immune dysfunction. The patient was treated initially with voriconazole and subsequently underwent surgical excision of the involved area. On follow-up, she has done extremely well with no evidence for recurrence. In summary, we describe the first case of chronic pulmonary aspergillosis in an immunocompetent patient with bronchial atresia. Hindawi Publishing Corporation 2014 2014-12-22 /pmc/articles/PMC4283422/ /pubmed/25587281 http://dx.doi.org/10.1155/2014/208963 Text en Copyright © 2014 Mazen O. Al-Qadi et al. https://creativecommons.org/licenses/by/3.0/ 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
Al-Qadi, Mazen O.
Reddy, Dereddi Raja S.
Larsen, Brandon T.
Iyer, Vivek N.
Chronic Pulmonary Aspergillosis Complicating Bronchial Atresia
title Chronic Pulmonary Aspergillosis Complicating Bronchial Atresia
title_full Chronic Pulmonary Aspergillosis Complicating Bronchial Atresia
title_fullStr Chronic Pulmonary Aspergillosis Complicating Bronchial Atresia
title_full_unstemmed Chronic Pulmonary Aspergillosis Complicating Bronchial Atresia
title_short Chronic Pulmonary Aspergillosis Complicating Bronchial Atresia
title_sort chronic pulmonary aspergillosis complicating bronchial atresia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283422/
https://www.ncbi.nlm.nih.gov/pubmed/25587281
http://dx.doi.org/10.1155/2014/208963
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