Clinical case of late diagnosis of cystic fibrosis in an adolescent with nasal polyposis
https://doi.org/10.31146/2949-4664-apps-3-2-66-71
Abstract
Cystic fibrosis is a hereditary disease caused by mutations in the CFTR gene. This leads to systemic involvement of the exocrine glands and chronic progression of pulmonary pathology. Сystic fibrosis is currently being transferred into the category of controllable chronic diseases owing to new effective targeted therapies, improved methods of early diagnostics, and greater attention to the patient’s quality of life. In this article, we preent a clinical case of cystic fibrosis in a 14-year-old child, where the diagnostic process began with a CT scan of the paranasal sinuses that revealed features of polypous polysinusitis.
About the Authors
N. M. Gaponova
Tula Children’s Regional Clinical Hospital
Russian Federation
Russian Federation
atalia M. Gaponova, Head of the Pulmonology Department, pediatric pulmonologist; chief specialist of the Ministry of Health of the Tula Region, member of the Russian Respiratory Society
39, Bondarenko str., Tula, 300010
D. A. Alimurzaeva
Tula Children’s Regional Clinical Hospital
Russian Federation
Russian Federation
Djamila A. Alimurzaeva, Pediatrician and Allergologist-Immunologist, Pulmonology Department
39, Bondarenko str., Tula, 300010
M. V. Zagryadskikh
Tula State University
Russian Federation
Russian Federation
Maria V. Zagryadskikh, Clinical Resident, Department of Internal Medicine
92, Lenin ave., Tula, 300012
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Review
For citations:
Gaponova N.M., Alimurzaeva D.A., Zagryadskikh M.V. Clinical case of late diagnosis of cystic fibrosis in an adolescent with nasal polyposis. Archives of Pediatrics and Pediatric Surgery. 2025;3(2):66-71. (In Russ.) https://doi.org/10.31146/2949-4664-apps-3-2-66-71
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