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Chronic hypersensitivity pneumonitis

Hypersensitivity pneumonitis (HSP) is a common interstitial lung disease resulting from inhalation of a large variety of antigens by susceptible individuals. The disease is best classified as acute and chronic. Chronic HSP can be fibrosing or not. Fibrotic HSP has a large differential diagnosis and...

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Autores principales: Pereira, Carlos AC, Gimenez, Andréa, Kuranishi, Lilian, Storrer, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036552/
https://www.ncbi.nlm.nih.gov/pubmed/27703382
http://dx.doi.org/10.2147/JAA.S81540
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author Pereira, Carlos AC
Gimenez, Andréa
Kuranishi, Lilian
Storrer, Karin
author_facet Pereira, Carlos AC
Gimenez, Andréa
Kuranishi, Lilian
Storrer, Karin
author_sort Pereira, Carlos AC
collection PubMed
description Hypersensitivity pneumonitis (HSP) is a common interstitial lung disease resulting from inhalation of a large variety of antigens by susceptible individuals. The disease is best classified as acute and chronic. Chronic HSP can be fibrosing or not. Fibrotic HSP has a large differential diagnosis and has a worse prognosis. The most common etiologies for HSP are reviewed. Diagnostic criteria are proposed for both chronic forms based on exposure, lung auscultation, lung function tests, HRCT findings, bronchoalveolar lavage, and biopsies. Treatment options are limited, but lung transplantation results in greater survival in comparison to idiopathic pulmonary fibrosis. Randomized trials with new antifibrotic agents are necessary.
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spelling pubmed-50365522016-10-04 Chronic hypersensitivity pneumonitis Pereira, Carlos AC Gimenez, Andréa Kuranishi, Lilian Storrer, Karin J Asthma Allergy Review Hypersensitivity pneumonitis (HSP) is a common interstitial lung disease resulting from inhalation of a large variety of antigens by susceptible individuals. The disease is best classified as acute and chronic. Chronic HSP can be fibrosing or not. Fibrotic HSP has a large differential diagnosis and has a worse prognosis. The most common etiologies for HSP are reviewed. Diagnostic criteria are proposed for both chronic forms based on exposure, lung auscultation, lung function tests, HRCT findings, bronchoalveolar lavage, and biopsies. Treatment options are limited, but lung transplantation results in greater survival in comparison to idiopathic pulmonary fibrosis. Randomized trials with new antifibrotic agents are necessary. Dove Medical Press 2016-09-21 /pmc/articles/PMC5036552/ /pubmed/27703382 http://dx.doi.org/10.2147/JAA.S81540 Text en © 2016 Pereira et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Pereira, Carlos AC
Gimenez, Andréa
Kuranishi, Lilian
Storrer, Karin
Chronic hypersensitivity pneumonitis
title Chronic hypersensitivity pneumonitis
title_full Chronic hypersensitivity pneumonitis
title_fullStr Chronic hypersensitivity pneumonitis
title_full_unstemmed Chronic hypersensitivity pneumonitis
title_short Chronic hypersensitivity pneumonitis
title_sort chronic hypersensitivity pneumonitis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036552/
https://www.ncbi.nlm.nih.gov/pubmed/27703382
http://dx.doi.org/10.2147/JAA.S81540
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