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Updated: Mar 3, 2026

Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study
Published on: April 11, 2018
Massive nasal polyposis in a patient with newly diagnosed cystic fibrosis
Małgorzata Olszowiec-Chlebna, Krzysztof Trzciński, Iwona Stelmach1
1Department of Pediatrics and Allergology, N. Copernicus Hospital, Medical University of Lodz, Poland. alergol@kopernik.lodz.pl.
Introduction:
Cystic fibrosis (CF) - is the most common fatal autosomal recessive disease in Caucasians. A number of reports have described patients who do not meet diagnostic criteria for cystic fibrosis. Atypical or nonclassic CF is characterised by normal or borderline sweat test, pancreatic sufficiency and a monosymptomatic phenotype. For these reasons clinicians should remain alert to the possibility of the occurrence of CF.
Case Report:
We described a case presentation of massive nasal polyposis and recurrent sinusitis leading to the diagnosis ofcystic fibrosis in a 11-year-old male.
Conclusion:
Our study indicates that chronic sinusitis and/or polyposis should raise the clinicians suspicion of a potential presentation of undiagnosed CF and require further investigations.
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