Results 111 to 120 of about 240,665 (151)
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Congenital dacryocystocele: Is there a familial predisposition?
International Journal of Pediatric Otorhinolaryngology, 2011Congenital 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 ...
James C Wang, Michael J Cunningham
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Archives of Ophthalmology, 1982
Four cases of congenital lacrimal sac distention were managed in an initially conservative manner to further elucidate the natural history of the condition and to formulate a more systematic approach to its treatment. In three cases, the abnormality resolved without nasolacrimal duct probing, with no adverse sequelae. In one case, dacryocystitis caused
G J, Harris, D, DiClementi
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Four cases of congenital lacrimal sac distention were managed in an initially conservative manner to further elucidate the natural history of the condition and to formulate a more systematic approach to its treatment. In three cases, the abnormality resolved without nasolacrimal duct probing, with no adverse sequelae. In one case, dacryocystitis caused
G J, Harris, D, DiClementi
openaire +2 more sources
Journal of Ultrasound in Medicine, 2005
The purpose of this series is to present our experience with cases of dacryocystocele diagnosed prenatally. The role of prenatal 3-dimensional sonography, as an adjunct to 2-dimensional sonography, in the prenatal assessment of these cases is emphasized.A retrospective review of cases was conducted. Information was obtained by reviewing the sonographic
Waldo Sepulveda
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The purpose of this series is to present our experience with cases of dacryocystocele diagnosed prenatally. The role of prenatal 3-dimensional sonography, as an adjunct to 2-dimensional sonography, in the prenatal assessment of these cases is emphasized.A retrospective review of cases was conducted. Information was obtained by reviewing the sonographic
Waldo Sepulveda
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The Treatment of Congenital Dacryocystocele
American Journal of Ophthalmology, 2006To determine the proper management of congenital dacryocystocele.Retrospective interventional case series.Clinical practice.Twenty-seven consecutive patients with 29 congenital dacryocystoceles who presented from 1987 through 2006.The charts were reviewed for the presence and age of onset of infection, methods and age of treatment, and response to ...
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Prenatal diagnosis of congenital dacryocystocele
International Journal of Pediatric Otorhinolaryngology, 2013Congenital bilateral dacryocystocele was diagnosed prenatally by ultrasonography in 3 female fetuses at 32.5 weeks gestation. After birth, first baby developed respiratory distress and was treated with endoscopic marsupialization of the cysts; the second baby had no respiratory symptoms and had spontaneous resolution of the cysts without surgery.
Mathilde, Bachelard-Serra +5 more
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Congenital Dacryocystocele: A Major Review
Ophthalmic Plastic & Reconstructive Surgery, 2019Purpose: To provide a systematic review of the literature on congenital dacryocystoceles (CDCs) and summarize their presentations, investigations, management, and outcomes. Methods: The authors performed a PubMed search of all articles published in English on CDCs.
Swati, Singh, Mohammad Javed, Ali
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Congenital Dacryocystocele with Intranasal Extension
European Journal of Ophthalmology, 2005Purpose Congenital dacryocystocele is a rare anomaly in the newborn child. The swelling of lachrymal sac is observed by birth and it is associated with obstruction of lachrymal system either above or below lachrymal sac.
C C, Teixeira +3 more
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Presentation and Management of Congenital Dacryocystocele
Pediatrics, 2008OBJECTIVE. Our goal was to report the presentation, complications, and treatment strategies for infants with congenital dacryocystocele. PATIENTS AND METHODS. We performed a retrospective chart review of all patients presenting with dacryocystoceles to Children's Hospital Boston between the years of 1997 and 2006. This study was approved
Rupa Krishnamurthy, Wong +1 more
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Nasolacrimal duct cysts in congenital dacryocystocele
Graefe's Archive for Clinical and Experimental Ophthalmology, 1994J B Saracco
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