Rhinosinusitis in the pediatric patient with cystic fibrosis

Christopher Fundakowski, Rosemary Ojo, Ramzi Younis

Research output: Contribution to journalArticle

2 Scopus citations

Abstract

Cystic fibrosis (CF) is a common autosomal recessive genetic disorder where a deletion mutation and subsequent downstream alteration in transmembrane regulator proteins results in increased mucus viscosity. CF manifests clinically with chronic multisystem inflammation and recurrent infections. Nearly all children with CF have chronic sinusitis, and a large majority will have concurrent sinonasal polyposis. Chronic sinusitis and sinonasal polyposis in pediatric patients with CF can be managed conservatively initially, though most will fail medical management and require surgical intervention. Unfortunately, symptom resolution is marginal and polyp recurrence rates are high. Currently, no cure exists for CF and the mainstay of treatment is to provide symptomatic relief, and minimize disease morbidity.

Original languageEnglish (US)
Pages (from-to)198-201
Number of pages4
JournalCurrent Pediatric Reviews
Volume10
Issue number3
StatePublished - Jan 1 2014

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Keywords

  • Cystic fibrosis
  • Pediatric
  • Rhinosinusitis
  • Sinusitis

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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