Antrochoanal polyps in children

Although relatively rare, antrochoanal polyps represent one of the most com mon types of polyp diagnosed in children without cystic fibrosis. In an att empt to better define this entity and discuss treatment options, the histor ies and operative reports of all 25 children (aged 17 years and younger) di agnosed with an antrochoanal polyp bem,een 1970 and 1997 at our institution were reviewed. All 25 children complained of nasal obstruction on presenta tion; other presenting symptoms included rhinorrhea (48%), snoring (36%), a nd mouth breathing (32%). All 25 patients were noted to have a mass in the nose on examination, and 16 (64%) also had a mass noted in the nasopharynx. All but I patient underwent surgical removal of the Polyp: intranasal avul sion only, 2 patients; Caldwell-Luc procedures, 10 patients; intranasal pro cedures, 8 patients; and endoscopic procedures, 4 patients. Mean time to fi rst recurrence was 44.5 months. Seven patients (29%) who underwent excision at our institution experienced recurrence, 3 after endoscopic procedures a nd 4 after intranasal procedures (with or without Caldwell-Luc; 1 of these patients had a second recurrence), Complications were unusual and included bleeding after pack removal (8.3%) and facial paresthesias (10%). Follow-up ranged from 2 days to almost 27 years and was aided by telephone interview s. We conclude that surgical treatment of these lesions is safe and effecti ve. Endoscopic removal may result in a higher recurrence rate.