Congenital dacryocystocele: Is there a familial predisposition?

James C. Wang, Michael J. Cunningham*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Congenital impatency of the nasolacrimal drainage system is relatively common. Dacryocystocele formation is an infrequent variant of such congenital nasolacrimal duct obstruction (NLDO). Congenital dacryocystocele typically manifests as a mass in the medial canthal region; alternatively the nasolacrimal expansion may present solely intranasally as a nasolacrimal duct cyst. Despite the relative frequency of congenital NLDO, there have been few reported familial cases. We report here two female siblings with congenital dacryocystocele, and review the etiology and potential inherited predisposition to this comparatively rare entity.

Original languageEnglish (US)
Pages (from-to)430-432
Number of pages3
JournalInternational journal of pediatric otorhinolaryngology
Volume75
Issue number3
DOIs
StatePublished - Mar 2011

Keywords

  • Congenital nasolacrimal obstruction
  • Dacryocystocele
  • Familial

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Otorhinolaryngology

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