Literature DB >> 21276064

Case report: Congenital dacryocystocele and dacryocystitis.

J Nicole F Fussell1, Thomas Wilson, Howard Pride.   

Abstract

Congenital dacryocystocele is a uncommon type of nasolacrimal duct obstruction. Differential diagnosis for masses in the medial canthal region of a newborn include encephalocele, hemangioma, nasal glioma, and dermoid cyst. Because of the risk of becoming infected (acute dacryocystitis) and potentially lethal due to septicemia, aggressive management, including admission for intravenous antibiotics and surgical removal, is now advocated by many pediatric ophthalmologists if the cyst cannot be decompressed. Because of the commonly associated nasal cyst, infants with nasolacrimal dacryocyctocele may also experience respiratory distress especially when breast-feeding. The following case of dacryocystocele, which had progressed to dacryocystitis, was misdiagnosed as an infantile hemangioma. It is important to diagnose this entity quickly and refer for appropriate antibiotic and surgical management to avoid more serious sequelae of sepsis and possible death.
© 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 21276064     DOI: 10.1111/j.1525-1470.2010.01365.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  1 in total

1.  Outcomes of lacrimal probing surgery as the first option in the treatment of congenital dacryocystocele.

Authors:  Cetin Akpolat; Selam Yekta Sendul; Ebru Turkoglu Unal; Egemen Karatas; Cemile Ucgul Atilgan; Mehmet Demir
Journal:  Ther Adv Ophthalmol       Date:  2021-07-09
  1 in total

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