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Ophthalmic Plastic & Reconstructive Surgery, 2012
A full-term baby girl showed a bluish mass at birth in the right medial canthal area. She later demonstrated dacryocystitis and cellulitis. Although probing was performed, it was unsuccessful, and the dacryocystitis and cellulitis worsened. Computed tomography showed a dilated lacrimal sac, an enlarged nasolacrimal canal and a nasal cyst.
Hirohiko, Kakizaki +4 more
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A full-term baby girl showed a bluish mass at birth in the right medial canthal area. She later demonstrated dacryocystitis and cellulitis. Although probing was performed, it was unsuccessful, and the dacryocystitis and cellulitis worsened. Computed tomography showed a dilated lacrimal sac, an enlarged nasolacrimal canal and a nasal cyst.
Hirohiko, Kakizaki +4 more
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Selection of surgical intervention for congenital dacryocystocele
European Journal of Ophthalmology, 2018Purpose: To evaluate the surgical intervention and its effect on congenital dacryocystocele. Methods: A total of 531 children with congenital dacryocystocele admitted to the Department of Ophthalmology of Beijing Children’s Hospital ...
Yi, Zhang +3 more
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Microdebridement of Intranasal Cysts Associated With Congenital Dacryocystoceles
Ophthalmic Plastic & Reconstructive Surgery, 2022Purpose: The surgical management of congenital dacryocystoceles has evolved in recent decades. The aim of this study was to explore the effectiveness of endoscopic examination and powered microdebridement in the management of nasal cysts associated with congenital dacryocystoceles. Methods:
Katie, Magoon +4 more
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Sonographic antenatal diagnosis of congenital dacryocystoceles
Journal of Clinical Ultrasound, 2012AbstractCongenital dacryocystoceles are a relatively rare variant of nasolacrimal duct obstruction, accounting for only 0.1% of infants with congenital nasolacrimal duct obstruction. We report a new case of bilateral congenital dacrocystoceles diagnosed in an otherwise uncomplicated fetal ultrasound examination during the 33rd week of pregnancy.
Sotirios, Sotiriou +3 more
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Congenital Nasolacrimal Duct Cysts in Dacryocystocele
Ophthalmology, 1991Cystic intranasal masses were found in seven newborn infants with congenital dacryocystocele. The cysts were a direct extension of the nasolacrimal duct, located beneath the inferior turbinate. Nasal obstruction was present in three infants and was severe enough to cause respiratory distress in two neonates with bilateral cysts.
T R, Grin, J S, Mertz, M, Stass-Isern
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Case Report: Congenital Dacryocystocele and Dacryocystitis
Pediatric Dermatology, 2011Abstract: Congenital dacryocystocele is a uncommon type of nasolacrimal duct obstruction. Differential diagnosis for masses in the medial canthal region of a newborn include encephalocele, hemangioma, nasal glioma, and dermoid cyst. Because of the risk of becoming infected (acute dacryocystitis) and potentially lethal due to septicemia, aggressive ...
J Nicole F, Fussell +2 more
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Endoscopic management of congenital dacryocystocele
Operative Techniques in Otolaryngology - Head and Neck Surgery, 2018Congenital dacryocystocele is a relatively rare oculonasal anomaly which can result in symptomatic obstruction of the nasolacrimal system. Techniques utilized in the management of this condition include nasolacrimal duct probing, endoscopic dacryocystorhinostomy, and transnasal marsupialization.
Vijay A Patel
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Bilateral Dacryocystoceles in Congenital Arhinia
Ophthalmic Plastic & Reconstructive SurgeryCongenital arhinia is a rare anomaly characterized by a syndrome called Bosma arhinia microphthalmia syndrome. A 22-year-old woman with a history of congenital arhinia presented with bilateral discharge and enlarged bilateral lacrimal sacs, with imaging consistent with bilateral dacryocystoceles and complete absence of nasal structures.
Lisa Y. Lin +2 more
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Congenital dacryocystocele: sonographic evaluation of 11 cases
Journal of AAPOS, 2018To report prenatal sonographic findings of congenital dacryocystocele.The medical records of all cases diagnosed with congenital dacryocystocele at a tertiary care center from 2003 to 2015 were reviewed retrospectively.Eleven cases of congenital dacryocystocele were analyzed. No accompanying fetal anatomic anomalies where detected. Mean maternal age at
Victor M Villegas, Angela Miranda-Rivas
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Congenital Dacryocystocele in Identical Twins
Ophthalmic Plastic & Reconstructive Surgery, 1985Identical twins were found to have unilateral congenital dacryocystoceles. Both were immediately probed, which resulted in resolution of one and recurrence in the second twin. The recurrent dacryocystocele was reprobed and the abnormality was resolved. Etiology and management are discussed.
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