Idiopathic pulmonary fibrosis classification
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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:
- 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
- ↑ "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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