Idiopathic pulmonary fibrosis overview: Difference between revisions
Created page with "__NOTOC__ {{Idiopathic pulmonary fibrosis }} {{CMG}} ==Overview== ==References== {{reflist|2}} {{WH}} {{WS}} Category:Pulmonology Category:Disease" |
|||
| Line 3: | Line 3: | ||
{{CMG}} | {{CMG}} | ||
==Overview== | ==Overview== | ||
''' [[Idiopathic]] Pulmonary Fibrosis (IPF)''', is a chronic progressive interstitial lung disease of unknown etiology. It is one of the two classic interstitial lung diseases, the other being sarcoidosis.<ref name="WMMT">{{cite book |title=The Washington Manual of Medical Therapeutics |last=Cooper |first=Daniel H. |coauthors=Andrew J. Krainik, Sam J. Lubner, Hilary E. L. Reno (eds.)|edition=32nd edition |publisher=Lippincott Williams & Wilkins |pages=276 |isbn=978-0781781251}}</ref> | |||
More specifically, '''IPF''' is defined as a distinctive type of ''chronic fibrosing interstitial pneumonia'' of unknown cause associated with a histological pattern of [[usual interstitial pneumonia]] (UIP).<ref name="ATS">{{cite journal |url=http://ajrccm.atsjournals.org/cgi/content/full/161/2/646 |title=Idiopathic Pulmonary Fibrosis: Diagnosis and Treatment |journal=American Journal of Respiratory and Critical Care Medicine |volume=161 |number=2 |month=February |year=2000 |pages=646-664}}</ref> | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Revision as of 19:21, 25 September 2012
|
Idiopathic pulmonary fibrosis Microchapters |
|
Differentiating Idiopathic pulmonary fibrosis from other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
Idiopathic pulmonary fibrosis overview On the Web |
|
American Roentgen Ray Society Images of Idiopathic pulmonary fibrosis overview |
|
Directions to Hospitals Treating Idiopathic pulmonary fibrosis |
|
Risk calculators and risk factors for Idiopathic pulmonary fibrosis overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Idiopathic Pulmonary Fibrosis (IPF), is a chronic progressive interstitial lung disease of unknown etiology. It is one of the two classic interstitial lung diseases, the other being sarcoidosis.[1]
More specifically, IPF is defined as a distinctive type of chronic fibrosing interstitial pneumonia of unknown cause associated with a histological pattern of usual interstitial pneumonia (UIP).[2]
References
- ↑ Cooper, Daniel H. The Washington Manual of Medical Therapeutics (32nd edition ed.). Lippincott Williams & Wilkins. p. 276. ISBN 978-0781781251. Unknown parameter
|coauthors=ignored (help) - ↑ "Idiopathic Pulmonary Fibrosis: Diagnosis and Treatment". American Journal of Respiratory and Critical Care Medicine. 161 (2): 646–664. 2000. Unknown parameter
|month=ignored (help)