Idiopathic pulmonary fibrosis classification: Difference between revisions
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{{Idiopathic pulmonary fibrosis }} | {{Idiopathic pulmonary fibrosis }} | ||
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==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 Acute Interstitial Pneumonia (AIP), Cryptogenic Organizing Pneumonia (COP), Respiratory Bronchiolitis–Interstitial Lung Disease (RB-ILD), and Desquamative Interstitial Pneumonia (DIP) | 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 Acute Interstitial Pneumonia (AIP), Cryptogenic Organizing Pneumonia (COP), Respiratory Bronchiolitis–Interstitial Lung Disease (RB-ILD), and Desquamative Interstitial Pneumonia (DIP) | ||
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** Major idiopathic interstitial pneumonia | ** Major idiopathic interstitial pneumonia | ||
** Rare 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: | * 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) | ** Acute or subacute: Acute Interstitial Pneumonia (AIP) and Cryptogenic Organizing Pneumonia (COP) | ||
** Chronic: Idiopathic Pulmonary Fibrosis (IPF) | ** Chronic: Idiopathic Pulmonary Fibrosis (IPF) | ||
** Smoking related: Respiratory Bronchiolitis–Interstitial Lung Disease (RB-ILD) and Desquamative Interstitial Pneumonia (DIP) | ** Smoking-related: Respiratory Bronchiolitis–Interstitial Lung Disease (RB-ILD) and Desquamative Interstitial Pneumonia (DIP) | ||
==References== | ==References== | ||
Revision as of 20:02, 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]; 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 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
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