Congenital Dacryocystocele: A Rare and Benign Nasolacrimal Duct Cyst Condition

Author:

Bonilla-Musoles Fernando,Castillo Juan Carlos,Jimenez Luis Carlos

Abstract

ABSTRACT Dacryocystocele is an uncommon congenital obliteration of the nasolacrimal drainage system. Based on a case diagnosed at 30 weeks gestation using two-dimensional (2D) and threedimensional (3D), its ultrasound characteristics as well as the evolution and therapeutic options applied in the scarce existing literature are described. How to cite this article Bonilla-Musoles F, Jimenez LC, Castillo JC. Congenital Dacryocystocele: A Rare and Benign Nasolacrimal Duct Cyst Condition. Donald School J Ultrasound Obstet Gynecol 2012;6(3):233-236.

Publisher

Jaypee Brothers Medical Publishing

Subject

Geriatrics and Gerontology,Radiology, Nuclear Medicine and imaging

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Congenital dacryocystocele: sonographic evaluation of 11 cases;Journal of American Association for Pediatric Ophthalmology and Strabismus;2018-10

2. Dacryocystocele on prenatal ultrasonography: diagnosis and postnatal outcomes;Ultrasonography;2014-09-27

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