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Updated: Jun 28, 2026

Transcanalicular Diode Laser-assisted Dacryocystorhinostomy for the Treatment of Primary Acquired Nasolacrimal Duct Obstruction
Published on: October 13, 2017
Presentation and management of congenital dacryocystocele
Rupa Krishnamurthy Wong1, Deborah K VanderVeen
1Department of Ophthalmology, Children's Hospital Boston, Boston, Massachusetts 02115, USA. rupa.krishnamurthy@childrens.harvard.edu
Insights
Congenital dacryocystocele in infants often requires intervention. Early referral and treatment are crucial to prevent complications like infection and respiratory compromise.
Area of Science:
- Ophthalmology
- Pediatric Surgery
Background:
- Congenital dacryocystocele is a common condition in newborns.
- It presents as a cyst-like swelling at the lower eyelid due to nasolacrimal duct obstruction.
Purpose of the Study:
- To describe the clinical presentation, complications, and treatment outcomes for congenital dacryocystocele.
- To evaluate the effectiveness of various treatment strategies.
Main Methods:
- Retrospective chart review of infants with congenital dacryocystocele.
- Data collected from Children's Hospital Boston between 1997 and 2006.
- Included patient demographics, presenting symptoms, complications, and treatments.
Main Results:
- 42 infants (46 eyes) were identified, presenting at a median age of 7 days.
- 65% of patients had dacryocystitis requiring antibiotics; 9.5% experienced respiratory compromise.
- Conservative treatment resolved 10 eyes; 78% required surgery, with office probing successful in 76% of cases.
Conclusions:
- Congenital dacryocystocele frequently necessitates surgical intervention despite potential for conservative resolution.
- Infection and respiratory compromise are significant complications.
- Early neonatal referral is recommended for timely management and prevention of complications.
Objective:
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 by the institutional review board.
Results:
Forty-two patients (46 eyes) were identified (18 male, 24 female), presenting at a median age of 7 days of life. Twenty-eight (65%) patients presented with cellulitis or dacryocystitis and required systemic antibiotics. Four (9.5%) patients presented with respiratory compromise. Resolution occurred with conservative treatment for 10 eyes, but 36 (78%) required surgical intervention. Seventeen (37%) eyes received probing in the office or nursery, and 13 (76%) were successful. Probing in the operating room was required for 21 patients, 8 of whom required marsupialization of an intranasal cyst.
Conclusions:
Although congenital dacryocystoceles may resolve with conservative measures, many become infected and require systemic antibiotic treatment, and most require surgical intervention. Referral in the early neonatal period can aid in timely intervention before complications such as infection occur.
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