Understanding the relationship between CF and nasal polyps is essential for early detection and effective management. This article delves into the causes, symptoms, diagnosis, and treatment options for nasal polyps in cystic fibrosis patients, offering valuable insights for patients, caregivers, and healthcare providers., Study objectives: Nasal polyps frequently appear in patients with cystic fibrosis (CF). The aims of this study were to focus on what problems (symptoms, endoscopic findings, and laboratory correlates) nasal polyps cause the CF patient, and how these correlate to the total health situation of this patient group., Polyposis was the initial symptom of cystic fibrosis in 13 patients. Common symptoms included obstruction to nasal air flow, mouth breathing, epistaxis, and rhinorrhea. Intranasal and oral corticosteroids and antihistamines were ineffective in preventing recurrences but did occasionally afford symptomatic relief of obstruction., While nasal polyps can occur in children, they are often associated with conditions like chronic sinusitis, allergic rhinitis, or cystic fibrosis. If left untreated, polyps may continue to grow and obstruct the nasal passages, thus requiring medical intervention., Objective To assess the incidence of nasal polyposis, the response to medical treatment, recurrence and the need for surgical intervention in children and adolescents with cystic fibrosis during a three-year follow-up., Cystic fibrosis (CF) is a life‐shortening, autosomal recessive disease that leads to abnormal electrolyte concentration in exocrine secretions. Secretion stasis in paranasal sinuses determines chronic rhinosinusitis (CRS) and nasal polyposis. Endoscopic sinus surgery is used to open the sinuses and allow medical treatment to work properly..