Congenital bilateral dacryocystocele: case report

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Andrea del Pilar Sierra Avila
Diana Carolina Hernández Rodríguez
Nicolás García Torres

Abstract

Introduction: Dacryocystocele is a rare congenital malformation secondary to nasolacrimal duct obstruction. It has an incidence of 0.1% of patients with congenital nasolacrimal duct obstruction, being found bilaterally in up to 25% of cases. Case Report: Two-month-old female infant with preseptal right periorbital cellulitis not associated with an entrance lesion, with an initial diagnosis of right dacryocystitis. On physical examination, a large abscessed mass in the lacrimal sac was evidenced in the right eye; in the left eye, there was an indurated area and slight reflux to the lacrimal sac pressure. Computed tomography of the orbits was performed with findings compatible with bilateral dacryocystocele. Discussion and conclusions: Knowing the presentation and possible complications associated with this pathology prevents significant patient morbidity. Most cases of dacryocystocele can be managed medically, however, cases associated with complications require timely surgical management.

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How to Cite
1.
Sierra Avila A del P, Hernández Rodríguez DC, García Torres N. Congenital bilateral dacryocystocele: case report. Acta otorrinolaringol cir cabeza cuello [Internet]. 2024Feb.7 [cited 2024Nov.21];51(4):297 - 300. Available from: https://revista.acorl.org.co/index.php/acorl/article/view/719
Section
Reportes de Casos

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