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Updated: Dec 16, 2025

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Transcanalicular Diode Laser-assisted Dacryocystorhinostomy for the Treatment of Primary Acquired Nasolacrimal Duct Obstruction
Published on: October 13, 2017
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Congenital lacrimal sac diverticulum
Teresa Salvá-Palomeque1, Pablo Muñoz-Ramón1, Nieves Alonso-Formento1
1Ophthalmology Department, Ramon y Cajal University Hospital.
Summary
Congenital nasolacrimal sac diverticulum caused recurrent dacryocystitis in an infant. Surgical removal of the diverticulum resolved the condition, highlighting a rare cause of infantile eye infections.
Area of Science:
- Ophthalmology
- Pediatric Surgery
- Anatomy
Background:
- Recurrent acute dacryocystitis in infants can significantly impact quality of life.
- Congenital nasolacrimal sac diverticulum is a rare anomaly, often asymptomatic.
- Prompt diagnosis and targeted intervention are crucial for managing pediatric eye conditions.
Observation:
- A 6-month-old boy presented with recurrent acute dacryocystitis from 3 months to 1 year of age.
- The underlying cause was identified as a congenital nasolacrimal sac diverticulum.
- The patient's lacrimal drainage system was determined to be patent.
Findings:
- An isolated diverticulectomy was successfully performed, excluding the need for dacryocystorhinostomy.
- The infant remained asymptomatic at a 6-month follow-up post-surgery.
- This case demonstrates the efficacy of diverticulectomy for symptomatic congenital nasolacrimal sac diverticulum.
Implications:
- Congenital nasolacrimal sac diverticulum should be considered in the differential diagnosis of infantile dacryocystitis.
- Isolated diverticulectomy is a viable surgical option for symptomatic cases with a patent lacrimal drainage system.
- Early surgical intervention can prevent complications and improve outcomes in pediatric ophthalmology.
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