Supernumerary nostril: a rare congenital deformity

被引:19
作者
Williams, A
Pizzuto, M
Brodsky, L
Perry, R
机构
[1] SUNY Buffalo, Childrens Hosp Buffalo, Sch Med & Biomed Sci, Dept Otolaryngol, Buffalo, NY 14222 USA
[2] SUNY Buffalo, Childrens Hosp Buffalo, Sch Med & Biomed Sci, Dept Pediat, Buffalo, NY 14222 USA
[3] SUNY Buffalo, Childrens Hosp Buffalo, Sch Med & Biomed Sci, Dept Plast Surg, Buffalo, NY 14222 USA
关键词
polyhinia; double nose; supernumerary nostril; accessory nostril; congenital nasal deformities; duplication anomalies of the nose;
D O I
10.1016/S0165-5876(98)00044-5
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Duplication anomalies of the nose include polyhinia (double nose) and supernumerary nostril (assessory nostril). These are rare congenital nasal deformities resulting from aberrant embryological development. Differential diagnoses include glioma, encephalocele, nasal dermoid, nasolacrimal 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 reported 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, anatomy and a thorough review of the literature are included. (C) 1998 Elsevier Science ireland Ltd. All rights reserved.
引用
收藏
页码:161 / 167
页数:7
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