Idiopathic pulmonary fibrosis classification: Difference between revisions

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{{CMG}}
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==Overview==
==Overview==
==Classification==
'''Idiopathic pulmonary fibrosis''' is a type of [[idiopathic interstitial pneumonia]] (IIP), which in turn is a type (or group) of interstitial lung diseases.<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>
Idiopathic interstitial pneumonias include:
* [[idiopathic pulmonary fibrosis]] (IPF) (the most common)
* [[nonspecific interstitial pneumonia]]
* [[cryptogenic organizing pneumonia]]
* [[acute interstitial pneumonia]]
* respiratory bronchiolitis-associated interstitial lung disease
* [[desquamative interstitial pneumonia]]
* [[lymphoid interstitial pneumonia]]
==References==
==References==
{{reflist|2}}
{{reflist|2}}

Revision as of 19:25, 25 September 2012

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Classification

Idiopathic pulmonary fibrosis is a type of idiopathic interstitial pneumonia (IIP), which in turn is a type (or group) of interstitial lung diseases.[1]

Idiopathic interstitial pneumonias include:

References

  1. "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 |month= ignored (help)

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