Pulmonary Alveolar Proteinosis [plicní alveolární proteinóza]
- Terms
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alveolární lipoproteinóza
plicní alveoly - proteinóza
Rosenův-Castlemanův-Liebowův syndrom
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Alveolar Proteinoses, Pulmonary
Alveolar Proteinosis, Pulmonary
Proteinoses, Pulmonary Alveolar
Proteinosis, Pulmonary Alveolar
Pulmonary Alveolar Proteinoses
A PULMONARY ALVEOLI-filling disease, characterized by dense phospholipoproteinaceous deposits in the alveoli, cough, and DYSPNEA. This disease is often related to, congenital or acquired, impaired processing of PULMONARY SURFACTANTS by alveolar macrophages, a process dependent on GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR.
- DUI
- D011649 MeSH Browser
- CUI
- M0018120
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 2
- CO
- complications 2
- CN
- congenital
- DI
- diagnosis 14
- DG
- diagnostic imaging 1
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 1
- EH
- ethnology
- ET
- etiology 8
- GE
- genetics 1
- HI
- history 1
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 4
- PP
- physiopathology 3
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery 1
- TH
- therapy 16
- UR
- urine
- VE
- veterinary
- VI
- virology
Pulmonary Alveolar Proteinosis, Acquired Disease MeSH Browser
Surfactant Metabolism Dysfunction, Pulmonary, 1 Disease MeSH Browser
Surfactant Metabolism Dysfunction, Pulmonary, 2 Disease MeSH Browser
Surfactant Metabolism Dysfunction, Pulmonary, 3 Disease MeSH Browser
Surfactant Metabolism Dysfunction, Pulmonary, 4 Disease MeSH Browser