Idiopathic pulmonary fibrosis classification: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
|||
| (2 intermediate revisions by one other user not shown) | |||
| Line 3: | Line 3: | ||
{{CMG}}; {{AE}} {{AEL}} | {{CMG}}; {{AE}} {{AEL}} | ||
==Overview== | ==Overview== | ||
Idiopathic pulmonary fibrosis is a disease among a large group of the interstitial lung diseases and particularly a subtype of the idiopathic interstitial pneumonia. The major group | Idiopathic pulmonary fibrosis is a disease among a large group of the interstitial lung diseases and particularly a subtype of the idiopathic interstitial pneumonia. The major group include [[acute interstitial pneumonia]] (AIP), [[cryptogenic organizing pneumonia]] (COP), [[respiratory bronchiolitis]]–[[interstitial lung disease]] (RB-ILD), and [[desquamative interstitial pneumonia]] (DIP). | ||
==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. | * 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 major forms of the idiopathic interstitial pneumonia include: | ||
* 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> | * The [[Idiopathic interstitial pneumonia|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 | ** Major idiopathic interstitial pneumonia | ||
** Rare idiopathic interstitial pneumonia | ** Rare idiopathic interstitial pneumonia | ||
** Unclassifiable idiopathic interstitial pneumonia | ** Unclassifiable 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: | * 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 | ** Acute or subacute: [[Acute interstitial pneumonia]] (AIP) and [[cryptogenic organizing pneumonia]] (COP) | ||
** Chronic: Idiopathic | ** Chronic: Idiopathic pulmonary fibrosis (IPF) | ||
** Smoking-related: Respiratory | ** Smoking-related: [[Respiratory bronchiolitis]]–[[interstitial lung disease]] (RB-ILD) and [[desquamative interstitial pneumonia]] (DIP) | ||
==References== | ==References== | ||
| Line 22: | Line 22: | ||
[[Category:Pulmonology]] | [[Category:Pulmonology]] | ||
[[Category: | [[Category:Medicine]] | ||
[[Category:Up-To-Date]] | |||
[[Category:Primary Care] | |||
Latest revision as of 18:39, 9 April 2018
|
Idiopathic pulmonary fibrosis Microchapters |
|
Differentiating Idiopathic pulmonary fibrosis from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
Idiopathic pulmonary fibrosis classification On the Web |
|
American Roentgen Ray Society Images of Idiopathic pulmonary fibrosis classification |
|
Directions to Hospitals Treating Idiopathic pulmonary fibrosis |
|
Risk calculators and risk factors for Idiopathic pulmonary fibrosis classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]
Overview
Idiopathic pulmonary fibrosis is a disease among a large group of the interstitial lung diseases and particularly a subtype of the idiopathic interstitial pneumonia. The major group include acute interstitial pneumonia (AIP), cryptogenic organizing pneumonia (COP), respiratory bronchiolitis–interstitial lung disease (RB-ILD), and desquamative interstitial pneumonia (DIP).
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 major forms of the idiopathic interstitial pneumonia include:
- 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
- Unclassifiable 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
|month=ignored (help)
Template:WH Template:WS [[Category:Primary Care]