Congenital dacryocystocele: Is there a familial predisposition?

被引：17

作者：

Wang, James C. ^{[1
]}

Cunningham, Michael J. ^{[1
]}

机构：

[1] Harvard Univ, Sch Med, Dept Otol & Laryngol, Dept Otolaryngol,Massachusetts Eye & Ear Infirm, Boston, MA 02114 USA

来源：

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY | 2011年 / 75卷 / 03期

关键词：

Dacryocystocele; Congenital nasolacrimal obstruction; Familial; NASOLACRIMAL DUCT; OBSTRUCTION; MANAGEMENT; MUCOCELE;

D O I：

10.1016/j.ijporl.2010.11.026

中图分类号：

R76 [耳鼻咽喉科学];

学科分类号：

100213 ;

摘要：

Congenital impatency of the nasolacrimal drainage system is relatively common. Dacryocystocele formation is an infrequent variant of such congenital nasolacrimal duct obstruction (NLDO). Congenital dacryocystocele typically manifests as a mass in the medial canthal region; alternatively the nasolacrimal expansion may present solely intranasally as a nasolacrimal duct cyst. Despite the relative frequency of congenital NLDO, there have been few reported familial cases. We report here two female siblings with congenital dacryocystocele, and review the etiology and potential inherited predisposition to this comparatively rare entity. Published by Elsevier Ireland Ltd.

引用

页码：430 / 432

页数：3

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