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Congenital bilateral dacryocystocele
Pedro Carneiro de Sousa1, Marta Neves1, Delfim Duarte1
1Hospital Pedro Hispano, Unidade Local de Saúde de Matosinhos Otorhinolaryngology, Travessa do Padre Amaro, number 169/229, Matosinhos 4455-033, Portugal.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|October 20, 2018
Summary
Congenital bilateral dacryocystocele, a rare condition, can cause neonatal respiratory distress in newborns. Conservative treatment led to spontaneous resolution of symptoms in a case report.
Area of Science:
- Neonatal Medicine
- Ophthalmology
- Otorhinolaryngology
Background:
- Newborns are obligate nasal breathers, making nasal obstruction a critical issue.
- Nasal obstruction in neonates can rapidly lead to cyanosis and hypoxemia.
- Congenital bilateral dacryocystocele is an uncommon but significant cause of neonatal respiratory distress.
Observation:
- A male neonate presented with severe respiratory distress.
- Physical examination revealed bilateral, polypoid, bluish nasal masses obstructing the inferior meatus.
- Imaging studies confirmed the presence of bilateral dacryocystocele.
Findings:
- The neonate's respiratory distress resolved following conservative management.
- Spontaneous drainage of the dacryocystocele occurred, alleviating the obstruction.
- Diagnosis of congenital dacryocystocele is primarily clinical, supported by imaging.
Implications:
- Congenital dacryocystocele should be considered in the differential diagnosis of neonatal respiratory distress.
- While treatment is debated, conservative management can be effective.
- Surgical intervention is reserved for cases with persistent respiratory obstruction unresponsive to conservative measures.

