2023, Number 4
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Acta de Otorrinolaringología CCC 2023; 51 (4)
Congenital bilateral dacryocystocele: case report
del Pilar Sierra-Ávila A, Hernández-Rodríguez DC, García-Torres N
Language: Spanish
References: 12
Page: 297-300
PDF size: 184.66 Kb.
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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