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State of the art in the diagnosis and management of interstitial lung disease

The interstitial lung diseases (ILDs) are a diverse group of disorders characterized by a varying combination of inflammation and fibrosis of the pulmonary parenchyma. Treatment and prognosis of ILD typically depend on the underlying ILD subtype, highlighting the importance of accurate classificatio...

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Detalles Bibliográficos
Autores principales: BUZAN, MARIA T. A., POP, CARMEN MONICA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iuliu Hatieganu University of Medicine and Pharmacy 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576791/
https://www.ncbi.nlm.nih.gov/pubmed/26528058
http://dx.doi.org/10.15386/cjmed-457
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author BUZAN, MARIA T. A.
POP, CARMEN MONICA
author_facet BUZAN, MARIA T. A.
POP, CARMEN MONICA
author_sort BUZAN, MARIA T. A.
collection PubMed
description The interstitial lung diseases (ILDs) are a diverse group of disorders characterized by a varying combination of inflammation and fibrosis of the pulmonary parenchyma. Treatment and prognosis of ILD typically depend on the underlying ILD subtype, highlighting the importance of accurate classification and diagnosis. Besides a thorough history and clinical examination, the protocol should include a 6-minute walk test, chest radiography, high-resolution computed tomography, biochemical analysis, pulmonary function tests, blood gas analysis, bronchoalveolar lavage, and, when necessary, a lung biopsy. The final diagnosis of ILD entities requires dynamic interaction between clinicians, radiologists and pathologists to reach a clinico-radiologic-pathologic diagnosis, the gold standard no longer being the histology but rather a multidisciplinary approach.
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spelling pubmed-45767912015-11-02 State of the art in the diagnosis and management of interstitial lung disease BUZAN, MARIA T. A. POP, CARMEN MONICA Clujul Med Review The interstitial lung diseases (ILDs) are a diverse group of disorders characterized by a varying combination of inflammation and fibrosis of the pulmonary parenchyma. Treatment and prognosis of ILD typically depend on the underlying ILD subtype, highlighting the importance of accurate classification and diagnosis. Besides a thorough history and clinical examination, the protocol should include a 6-minute walk test, chest radiography, high-resolution computed tomography, biochemical analysis, pulmonary function tests, blood gas analysis, bronchoalveolar lavage, and, when necessary, a lung biopsy. The final diagnosis of ILD entities requires dynamic interaction between clinicians, radiologists and pathologists to reach a clinico-radiologic-pathologic diagnosis, the gold standard no longer being the histology but rather a multidisciplinary approach. Iuliu Hatieganu University of Medicine and Pharmacy 2015 2015-04-15 /pmc/articles/PMC4576791/ /pubmed/26528058 http://dx.doi.org/10.15386/cjmed-457 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
spellingShingle Review
BUZAN, MARIA T. A.
POP, CARMEN MONICA
State of the art in the diagnosis and management of interstitial lung disease
title State of the art in the diagnosis and management of interstitial lung disease
title_full State of the art in the diagnosis and management of interstitial lung disease
title_fullStr State of the art in the diagnosis and management of interstitial lung disease
title_full_unstemmed State of the art in the diagnosis and management of interstitial lung disease
title_short State of the art in the diagnosis and management of interstitial lung disease
title_sort state of the art in the diagnosis and management of interstitial lung disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576791/
https://www.ncbi.nlm.nih.gov/pubmed/26528058
http://dx.doi.org/10.15386/cjmed-457
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