2011
DOI: 10.4193/rhino10.225
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Nasal polyposis and cystic fibrosis(CF): review of the literature

Abstract: The aim of this study was to address whether NP might be a predictive factor for severity of CF. The authors collected data from the literature on NP as a unique or associated sign in CF and reviewed the clinical and molecular aspects of CF associated with NP. CF genotypes and clinical severity in NP(+) vs. NP(-) patients were reviewed, taking into account pulmonary function, frequency of P. aeruginosa lung infection, frequency of allergy, nutritional status, and exocrine pancreatic function. The CFTR gene was… Show more

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Cited by 32 publications
(10 citation statements)
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“…Chinese and European polyps cannot be discriminated based on endoscopy but show a very different inflammatory pattern. The same holds true for polyps in patients with CF compared to non‐CF polyps 22, 23…”
Section: Discussionmentioning
confidence: 73%
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“…Chinese and European polyps cannot be discriminated based on endoscopy but show a very different inflammatory pattern. The same holds true for polyps in patients with CF compared to non‐CF polyps 22, 23…”
Section: Discussionmentioning
confidence: 73%
“…The same holds true for polyps in patients with CF compared to non-CF polyps. 22,23 We dichotomized the data to account for the symptom frequency based on a symptom score of !2. This means patients grade their symptom as ''a mild or slight problem'' or worse.…”
Section: Discussionmentioning
confidence: 99%
“…Many adult PwCF develop comorbid chronic rhinosinusitis (CRS) due to an inability to clear thick secretions from the upper airway and paranasal sinuses. Over half of adults with CF report symptomatic sinus disease, two-thirds have nasal polyposis, and nearly all have radiologic or endoscopic sinus inflammation ( 4 10 ). CF-related CRS is detrimental to quality of life (QOL) and associated with substantial productivity loss ( 11 16 ).…”
mentioning
confidence: 99%
“…[90][91][92] Premorbid conditions as risk factors for CRS Patients with CF may constitute up to approximately 5% of patients with CRS, 86,93 with the incidence of CRS in CF ranging up to 100% and the incidence of NP ranging up to 50% depending on the study. [94][95][96] Similarly, patients with primary ciliary dyskinesia, which may be due to over 30 different gene mutations and has an incidence of 1 in 10,000-20,000 live births, 97 have up to 100% lifetime risk of developing CRS due to the associated deficit in mucociliary clearance. 98 Granulomatous diseases (eg, sarcoidosis) and vasculitides (eg, granulomatosis with polyangiitis [GPA] or eosinophilic granulomatosis with polyangiitis [EGPA]) include CRS as one of their disease manifestations and may occur in up to 3% of patients with CRS.…”
Section: Demographic Risk Factors For Crsmentioning
confidence: 99%