Short Cilia, Immunodeficiency, and Cystic Fibrosis in a Mother-Daughter Pair
Authors:
Open Access
- 10 June 2024
- journal article
- research article
- Published by SAGE Publications in Ear, Nose & Throat Journal
Abstract
Patients with chronic rhinosinusitis (CRS) that is refractory to maximal medical and surgical therapy should be evaluated for other primary conditions. Cystic fibrosis (CF), primary immunodeficiency (PID), and primary ciliary dyskinesia (PCD) are potential risk factors for refractory CRS. These conditions present with variable disease severity and diagnosis may be delayed into adulthood. We report a case of a mother-daughter pair with CRS refractory to maximal medical management. The patients were further evaluated and found to have features consistent with CF, PID, and PCD. All 3 are rare disorders and thought to cause CRS in isolation. Patients with refractory CRS should be further evaluated to identify alternative diagnoses and ensure proper management. Refractory CRS may be multifactorial, with different risk factors simultaneously contributing to its persistence.Keywords
This publication has 20 references indexed in Scilit:
- Primary ciliary dyskinesia: An update on contemporary diagnosisInternational Forum of Allergy & Rhinology, 2023
- Evaluation and treatment of rhinosinusitis with primary antibody deficiency in adults: Evidence‐based review with recommendationsInternational Forum of Allergy & Rhinology, 2023
- The challenge of diagnosing primary ciliary dyskinesia: a commentary on various causative genes and their pathogenic variantsJournal of Human Genetics, 2023
- International consensus statement on allergy and rhinology: rhinosinusitis 2021International Forum of Allergy & Rhinology, 2020
- Medical and surgical treatment outcomes in patients with chronic rhinosinusitis and immunodeficiency: a systematic reviewInternational Forum of Allergy & Rhinology, 2020
- The diagnosis of cystic fibrosisLa Presse Médicale, 2017
- Primary immunodeficiency and recalcitrant chronic sinusitis: a systematic reviewInternational Forum of Allergy & Rhinology, 2016
- International Consensus Document (ICON): Common Variable Immunodeficiency DisordersThe Journal of Allergy and Clinical Immunology: In Practice, 2016
- Atypical Cystic Fibrosis and CFTR-Related DiseasesClinical Reviews in Allergy & Immunology, 2008
- Abnormal paranasal sinuses in patients with cystic fibrosis of the pancreasPediatric Radiology, 1980