Idiopathic pulmonary fibrosis classification: Difference between revisions
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==Overview== | ==Overview== | ||
==Classification== | ==Classification== | ||
* Idiopathic pulmonary fibrosis is a disease among a large group of the interstitial lung diseases and particularly a subtype of the idipathic interstitial pneumonia. | |||
* The idiopathic interstitial pneumonias are classified by the American Thoracic Society/European Respiratory Society (ATS/ERS) into three main groups:<ref name="ATS2">{{cite journal |url=http://ajrccm.atsjournals.org/cgi/content/full/165/2/277 |title=American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias |journal=American Journal of Respiratory and Critical Care Medicine |volume=165 |number=2 |month=January |year=2002 |pages=277-304}}</ref> | |||
** Major idiopathic interstitial pneumonia | |||
* | ** Rare idiopathic interstitial pneumonia | ||
* | ** Unclassificable idiopathic interstitial pneumonia | ||
* | * The idiopathic interstitial fibrosis is the chronic form of the idiopathic interstitial pneumonia. Other forms of the idiopathic interstitial pneumonia include the following: | ||
** Acute or subacute: Acute Interstitial Pneumonia (AIP) and Cryptogenic Organizing Pneumonia (COP) | |||
* | ** Chronic: Idiopathic Pulmonary Fibrosis (IPF) | ||
* | ** Smoking related: Respiratory Bronchiolitis–Interstitial Lung Disease (RB-ILD) and Desquamative Interstitial Pneumonia (DIP) | ||
* | |||
==References== | ==References== | ||
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{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
[[Category:Pulmonology]] | [[Category:Pulmonology]] | ||
[[Category:Disease]] | [[Category:Disease]] | ||
Revision as of 19:58, 12 February 2018
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Differentiating Idiopathic pulmonary fibrosis from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Classification
- Idiopathic pulmonary fibrosis is a disease among a large group of the interstitial lung diseases and particularly a subtype of the idipathic interstitial pneumonia.
- The idiopathic interstitial pneumonias are classified by the American Thoracic Society/European Respiratory Society (ATS/ERS) into three main groups:[1]
- Major idiopathic interstitial pneumonia
- Rare idiopathic interstitial pneumonia
- Unclassificable idiopathic interstitial pneumonia
- The idiopathic interstitial fibrosis is the chronic form of the idiopathic interstitial pneumonia. Other forms of the idiopathic interstitial pneumonia include the following:
- Acute or subacute: Acute Interstitial Pneumonia (AIP) and Cryptogenic Organizing Pneumonia (COP)
- Chronic: Idiopathic Pulmonary Fibrosis (IPF)
- Smoking related: Respiratory Bronchiolitis–Interstitial Lung Disease (RB-ILD) and Desquamative Interstitial Pneumonia (DIP)
References
- ↑ "American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias". American Journal of Respiratory and Critical Care Medicine. 165 (2): 277–304. 2002. Unknown parameter
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