Idiopathic pulmonary fibrosis classification: Difference between revisions

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==Overview==
==Overview==
==Classification==
==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 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>
Idiopathic interstitial pneumonias include:
** Major idiopathic interstitial pneumonia
* [[idiopathic pulmonary fibrosis]] (IPF) (the most common)
** Rare idiopathic interstitial pneumonia
* [[nonspecific interstitial pneumonia]]
** Unclassificable idiopathic interstitial pneumonia  
* [[cryptogenic organizing 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 interstitial pneumonia]]
** Acute or subacute: Acute Interstitial Pneumonia (AIP) and Cryptogenic Organizing Pneumonia (COP)
* respiratory bronchiolitis-associated interstitial lung disease
** Chronic: Idiopathic Pulmonary Fibrosis (IPF)
* [[desquamative interstitial pneumonia]]
** Smoking related: Respiratory Bronchiolitis–Interstitial Lung Disease (RB-ILD) and Desquamative Interstitial Pneumonia (DIP)
* [[lymphoid interstitial pneumonia]]


==References==
==References==
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[[Category:Pulmonology]]
[[Category:Pulmonology]]
[[Category:Disease]]
[[Category:Disease]]

Revision as of 19:58, 12 February 2018

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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

  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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