SUPERNUMERARY NOSTRIL - A RARE CONGENITAL DEFORMITY

Citation
A. Williams et al., SUPERNUMERARY NOSTRIL - A RARE CONGENITAL DEFORMITY, International journal of pediatric otorhinolaryngology, 44(2), 1998, pp. 161-167
Citations number
8
Categorie Soggetti
Otorhinolaryngology,Pediatrics
ISSN journal
01655876
Volume
44
Issue
2
Year of publication
1998
Pages
161 - 167
Database
ISI
SICI code
0165-5876(1998)44:2<161:SN-ARC>2.0.ZU;2-#
Abstract
Duplication anomalies of the nose include polyhinia (double nose) and supernumerary nostril (assessory nostril). These are rare congenital n asal deformities resulting from aberrant embryological development. Di fferential diagnoses include glioma, encephalocele, nasal dermoid, nas olacrimal duct duplication, mid facial cleft and proboscis lateralis ( K. Nakamura, T. Onizuka. Plast. Reconstr. Surg. 80 (3) (1987) 436-441) . Our review of the English language literature revealed eight reporte d cases of duplication anomalies of the nose. Four of these were cases of polyrhinia (double nose). Of the cases remaining, one patient had a supernumerary nostril in association with a cleft lip, leaving only three reported cases of an isolated supernumerary nostril. We present a newborn infant with an isolated right supernumerary nostril. MRI, CT and photographic documentation are provided. Pertinent embryology, an atomy and a thorough review of the literature are included. (C) 1998 E lsevier Science ireland Ltd. All rights reserved.