Structured Summary
Abstract
A group of interstitial lung diseases with no known etiology. There are several entities with varying patterns of inflammation and fibrosis. They are classified by their distinct clinical-radiological-pathological features and prognosis. They include IDIOPATHIC PULMONARY FIBROSIS; CRYPTOGENIC ORGANIZING PNEUMONIA; and others.
MeSH Record
Classification
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MeSH Record
Synonyms
5 entry terms
- Idiopathic Interstitial Pneumonia
- Interstitial Pneumonia, Idiopathic
- Interstitial Pneumonias, Idiopathic
- Pneumonia, Idiopathic Interstitial
- Pneumonias, Idiopathic Interstitial
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2009
MeSH Record
Previous Indexing
- Lung Diseases, Interstitial (1993-2008)
- Pulmonary Fibrosis (1972-1992)
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AMA Style
References
- National Library of Medicine. Idiopathic Interstitial Pneumonias. Medical Subject Headings (MeSH). 2026. Unique ID D054988. http://id.nlm.nih.gov/mesh/2026/D054988
- Idiopathic Interstitial Pneumonias. In: Wikipedia. https://en.wikipedia.org/wiki/Idiopathic_interstitial_pneumonia
- Idiopathic Interstitial Pneumonias. In: Wikidata. https://www.wikidata.org/wiki/Q1790424