Idiopathic Pulmonary Fibrosis [idiopatická plicní fibróza]
- Terms
-
familiární idiopatická plicní fibróza
idiopatická plicní fibróza familiární
intersticiální plicní fibróza
IPF
kryptogenní fibrotizující alveolitida
kryptogenní fibrózující alveolitida
obvyklá intersticiální pneumonie
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Cryptogenic Fibrosing Alveolitis
Familial Idiopathic Pulmonary Fibrosis
Fibrocystic Pulmonary Dysplasia
Fibrosing Alveolitis, Cryptogenic
Idiopathic Fibrosing Alveolitis, Chronic Form
Idiopathic Pulmonary Fibrosis, Familial
Interstitial Pneumonitis, Usual
Pulmonary Fibrosis, Idiopathic
Usual Interstitial Pneumonia
A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change.
- Annotation
- PULMONARY FIBROSIS is also available
- k dipozici je i deskriptor PLICNÍ FIBRÓZA
- DUI
- D054990 MeSH Browser
- CUI
- M0511887
- Previous indexing
- Pulmonary Fibrosis (1964-2008)
- History note
- 2009
- Public note
- 2009
Allowable subheadings
- BL
- blood 2
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 3
- CO
- complications 13
- CN
- congenital
- DI
- diagnosis 119
- DG
- diagnostic imaging 34
- DH
- diet therapy 2
- DT
- drug therapy 154
- EC
- economics 1
- EM
- embryology
- EN
- enzymology 1
- EP
- epidemiology 26
- EH
- ethnology
- ET
- etiology 27
- GE
- genetics 13
- HI
- history 3
- IM
- immunology 5
- ME
- metabolism 3
- MI
- microbiology 2
- MO
- mortality 17
- NU
- nursing
- PS
- parasitology
- PA
- pathology 49
- PP
- physiopathology 33
- PC
- prevention & control 2
- PX
- psychology 1
- RT
- radiotherapy 2
- RH
- rehabilitation 5
- SU
- surgery 2
- TH
- therapy 60
- UR
- urine
- VE
- veterinary 1
- VI
- virology