Idiopathic pulmonary fibrosis: a clinical case of long-term follow-up
Autor: | Galina L. Ignatova, Elena V. Blinova, Maria S. Belsner, Marina A. Korotkaia |
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Jazyk: | ruština |
Rok vydání: | 2022 |
Předmět: | |
Zdroj: | Consilium Medicum, Vol 24, Iss 9, Pp 640-644 (2022) |
Druh dokumentu: | article |
ISSN: | 2075-1753 2542-2170 20751753 |
DOI: | 10.26442/20751753.2022.9.201962 |
Popis: | Idiopathic pulmonary fibrosis is a specific form of chronic progressive fibrotic interstitial pneumonia of unknown etiology. Over the past decade, significant progress has been made in developing and utilizing a diagnostic algorithm for patients with idiopathic pulmonary fibrosis, involving analysis of clinical, laboratory, and instrumental data, primarily the results of high-resolution chest computed tomography. Early antifibrotic therapy can alter the disease course, slow its progression, and improve the prognosis. |
Databáze: | Directory of Open Access Journals |
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