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fibróza pľúcna idiopatická
Č. záznamu d054990 Dátum 06.06.2025 Typ M - MESH Tematický termín fibróza pľúcna idiopatická Iný termín Angličtina (Pseudonym) Cryptogenic Fibrosing Alveolitis
Slovenčina (Pseudonym) alveolitída fibrozujúca kryptogénna
MDT C08.381.483.652.500 Poznámka 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. 
predmetové heslo
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