Literature DB >> 2268602

Stevens-Johnson syndrome with associated nasolacrimal duct obstruction treated with dacryocystorhinostomy and Crawford silicone tube insertion.

J D Auran1, A Hornblass, N D Gross.   

Abstract

Although Stevens-Johnson syndrome (SJS) has long been recognized as a cause of punctal and canalicular obstruction, nasolacrimal duct obstruction secondary to SJS is rare and has not been reported in the ophthalmologic literature. Keratoconjunctivitis sicca, entropion, and trichiasis are well-known complications of SJS that may require measures to supplement or preserve tears. Lacrimal drainage system obstruction may occasionally occur in the face of relatively normal tearing, resulting in clinically significant epiphora. We report two cases of SJS, one associated with epidemic keratoconjunctivitis, that led to nasolacrimal duct obstruction and canalicular obstruction or stenosis. Epiphora and, in one case, dacryocystitis, necessitated dacryocystorhinostomy and Crawford tube insertion.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2268602     DOI: 10.1097/00002341-199003000-00010

Source DB:  PubMed          Journal:  Ophthalmic Plast Reconstr Surg        ISSN: 0740-9303            Impact factor:   1.746


  1 in total

1.  Bilateral conjunctival retention cysts in the aftermath of Stevens-Johnson syndrome.

Authors:  Gurdeep Singh; Revathi Rajaraman; Anita Raghavan; Manikandan Palanisamy
Journal:  Indian J Ophthalmol       Date:  2008 Jan-Feb       Impact factor: 1.848

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.