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Abstract
Congenital dacryocystocele: five clinical cases. Congenital dacryocystocele (CDC) is recognised as a cause of nasal airway obstruction or respiratory distress in newborns. CDC is caused by the distal obstruction of the lachrymal duct and presents as a cystic formation in the inferior meatus. We discuss five cases of dacryocystocele, together with surgical management and outcome. Endoscopic endonasal marsupialisation and appropriate postoperative care resulted in definitive recovery for all patients. In newborns or infants with nasal obstruction, CDC should be considered in the differential diagnosis, and prompt endoscopic endonasal marsupialisation is mandatory.
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Article Info
Published In
Journal
B-ENT
Volume / Issue
Volume 4 · Issue 3
Pages
141-145
History
Published Online
September 15, 2008
Affiliations
C. Hupin
Department of Otorhinolaryngology
N. Lévèque
Department of Otorhinolaryngology and Head and Neck Surgery, University of Louvain, Cliniques Saint Luc, Brussels, Belgium
Ph. Eloy
ENT Department, CHU UCL Namur, Site de Godinne, Yvoir, Belgium
B. Bertrand
ENT Department, CHU de Mont-Godinne, Yvoir
Ph. Rombaux
Department of Otorhinolaryngology, Université Catholique de Louvain, Cliniques Universitaires Saint Luc, Brussels, Belgium, Institute of Neuroscience
Cite this Article
Hupin, C., Lévèque, N., Eloy, P., Bertrand, B., & Rombaux, P. (2008). Congenital dacryocystocele: five clinical cases. B-ENT, 4(3), 141–145. Retrieved from https://www.b-ent.be/index.php/pub/article/view/191
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