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Histologische Klassifikation interstitieller Lungenerkrankungen

The 2002 ATS/ERS consensus classification of idiopathic interstitial pneumonias standardizes definitions and criteria for classification and diagnosis of idiopathic interstitial pneumonias and replaces previous classifications. Based on clinico-radiologic-pathologic criteria seven entities were defi...

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Autor principal: Dekan, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Steinkopff Verlag 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101525/
https://www.ncbi.nlm.nih.gov/pubmed/12624798
http://dx.doi.org/10.1007/s00393-003-0476-0
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author Dekan, Gerhard
author_facet Dekan, Gerhard
author_sort Dekan, Gerhard
collection PubMed
description The 2002 ATS/ERS consensus classification of idiopathic interstitial pneumonias standardizes definitions and criteria for classification and diagnosis of idiopathic interstitial pneumonias and replaces previous classifications. Based on clinico-radiologic-pathologic criteria seven entities were defined: idiopathic pulmonary fibrosis, nonspecific interstitial pneumonia, cryptogenic organizing pneumonia, acute interstitial pneumonia, respiratory bronchiolitis-associated interstitial lung disease, desquamative interstitial pneumonia and lymphoid interstitial pneumonia. The following paper includes a brief overview of the histopathological diagnosis of these entities as compared to other diffuse interstitial pulmonary diseases and pulmonary manifestations of collagenvascular diseases.
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spelling pubmed-71015252020-03-31 Histologische Klassifikation interstitieller Lungenerkrankungen Dekan, Gerhard Z Rheumatol Beitrag Zum Schwerpunktthema The 2002 ATS/ERS consensus classification of idiopathic interstitial pneumonias standardizes definitions and criteria for classification and diagnosis of idiopathic interstitial pneumonias and replaces previous classifications. Based on clinico-radiologic-pathologic criteria seven entities were defined: idiopathic pulmonary fibrosis, nonspecific interstitial pneumonia, cryptogenic organizing pneumonia, acute interstitial pneumonia, respiratory bronchiolitis-associated interstitial lung disease, desquamative interstitial pneumonia and lymphoid interstitial pneumonia. The following paper includes a brief overview of the histopathological diagnosis of these entities as compared to other diffuse interstitial pulmonary diseases and pulmonary manifestations of collagenvascular diseases. Steinkopff Verlag 2003 /pmc/articles/PMC7101525/ /pubmed/12624798 http://dx.doi.org/10.1007/s00393-003-0476-0 Text en © Steinkopff Verlag 2003 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Beitrag Zum Schwerpunktthema
Dekan, Gerhard
Histologische Klassifikation interstitieller Lungenerkrankungen
title Histologische Klassifikation interstitieller Lungenerkrankungen
title_full Histologische Klassifikation interstitieller Lungenerkrankungen
title_fullStr Histologische Klassifikation interstitieller Lungenerkrankungen
title_full_unstemmed Histologische Klassifikation interstitieller Lungenerkrankungen
title_short Histologische Klassifikation interstitieller Lungenerkrankungen
title_sort histologische klassifikation interstitieller lungenerkrankungen
topic Beitrag Zum Schwerpunktthema
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101525/
https://www.ncbi.nlm.nih.gov/pubmed/12624798
http://dx.doi.org/10.1007/s00393-003-0476-0
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