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Updated: Mar 19, 2026

Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study
Published on: April 11, 2018
Paediatric nasal polyps in cystic fibrosis
Mohd Afiq Mohd Slim1, David Dick1, Keith Trimble1
1Department of Ear, Nose and Throat, Royal Victoria Hospital, Belfast, UK.
Insights
Cystic fibrosis (CF) patients often develop nasal polyps. This case highlights functional endoscopic sinus surgery (FESS) providing symptom relief and improved facial appearance in a young CF patient with nasal polyposis.
Area of Science:
- Otolaryngology
- Pediatric Pulmonology
- Medical Genetics
Background:
- Cystic Fibrosis (CF) is a genetic disorder increasing the risk of sinonasal complications, including nasal polyposis.
- Nasal polyps in CF patients can lead to significant upper airway obstruction and facial deformities.
- The efficacy of early surgical intervention for CF-related nasal polyposis remains debated.
Observation:
- A 17-month-old child with CF presented with hypertelorism, astigmatism, nasal discharge, and noisy breathing.
- Imaging revealed bilateral ethmoid mucoceles.
- Surgical findings included bilateral soft tissue masses obstructing the nasal cavity.
Findings:
- Histological examination confirmed inflammatory nasal polyposis characteristic of CF.
- The patient underwent polypectomy and bilateral mega-antrostomies.
- Post-operative assessment showed significant relief of upper airway symptoms and normalization of facial appearance.
Implications:
- This case suggests potential benefits of functional endoscopic sinus surgery (FESS) for symptom management in pediatric CF patients with nasal polyposis.
- While recurrence rates are a concern, FESS may improve quality of life and cosmetic outcomes.
- Further research is needed to define the optimal surgical timing and long-term impact of FESS in this population.
Abstract:
Patients with cystic fibrosis (CF) are at increased risk of nasal polyps. We present the case of a 17-month-old Caucasian patient with CF who presented with hypertelorism causing cycloplegic astigmatism, right-sided mucoid discharge, snoring and noisy breathing. Imaging suggested bilateral mucoceles in the ethmoid sinuses. Intraoperatively, bilateral soft tissue masses were noted, and both posterior choanae were patent. Polypectomy and bilateral mega-antrostomies were performed. Histological examination revealed inflammatory nasal polyposis typical of CF. The role of early functional endoscopic sinus surgery (FESS) in children with CF nasal polyposis remains questionable as the recurrence rate is higher, and no improvement in pulmonary function has been shown. Our case, however, clearly demonstrates the beneficial upper airway symptom relief and normalisation of facial appearance following FESS in a child with this condition.
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