Management of Large Conjunctival Cysts in a Patient with Stevens-Johnson Syndrome: A Case Report and Review of the Literature

Stevens-Johnson syndrome (SJS) is a life-threatening mucocutaneous disease with various etiologies including drugs, infections, and malignancies. Ocular manifestations of SJS vary from the membrane, symblepharon formation, and epithelial defect in the acute phase to trichiasis, eyelid margin keratin...

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Main Authors: Sadid Hooshmandi, Kiana Hassanpour, Amirreza Veisi, Vahid Movafaghi, Farideh Langari, Mohammad-Mehdi Sadoughi, Mohammad Ali Javadi
Format: Article
Language:English
Published: Karger Publishers 2023-10-01
Series:Case Reports in Ophthalmology
Subjects:
Online Access:https://beta.karger.com/Article/FullText/533648
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author Sadid Hooshmandi
Kiana Hassanpour
Amirreza Veisi
Vahid Movafaghi
Farideh Langari
Mohammad-Mehdi Sadoughi
Mohammad Ali Javadi
author_facet Sadid Hooshmandi
Kiana Hassanpour
Amirreza Veisi
Vahid Movafaghi
Farideh Langari
Mohammad-Mehdi Sadoughi
Mohammad Ali Javadi
author_sort Sadid Hooshmandi
collection DOAJ
description Stevens-Johnson syndrome (SJS) is a life-threatening mucocutaneous disease with various etiologies including drugs, infections, and malignancies. Ocular manifestations of SJS vary from the membrane, symblepharon formation, and epithelial defect in the acute phase to trichiasis, eyelid margin keratinization, and lacrimal duct obstruction in the chronic phase. A 13-year-old boy with a history of drug-induced SJS presented to our clinic complaining of a mass in the nasal side and inferior fornix of the right eye from 1 year ago. The mass-like lesion in the medial side of the right eye was accompanied by ankyloblepharon, symblepharon, and ptosis and limited ocular movement. Orbital imaging showed cystic lesions on the medial side of the right globe and the inferior fornix. Two large cysts were entirely surgically excised. Histopathologic investigation revealed conjunctival tissue with nonkeratinized epithelium and goblet cells. There was no sign of conjunctival cyst recurrence or symblepharon formation on the 6th-month follow-up. The inferior fornix achieved acceptable depth and the ocular movements became normal.
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spelling doaj.art-42f67f93b32e46f084b3b1c7013fa0512023-11-02T10:50:46ZengKarger PublishersCase Reports in Ophthalmology1663-26992023-10-0114152853410.1159/000533648533648Management of Large Conjunctival Cysts in a Patient with Stevens-Johnson Syndrome: A Case Report and Review of the LiteratureSadid Hooshmandi0Kiana Hassanpour1Amirreza Veisi2Vahid Movafaghi3Farideh Langari4Mohammad-Mehdi Sadoughi5Mohammad Ali Javadi6Ophthalmic Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, Tehran, IranOphthalmic Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, Tehran, IranOphthalmic Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, Tehran, IranOphthalmic Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, Tehran, IranOphthalmic Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, Tehran, IranOphthalmic Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, Tehran, IranOphthalmic Research Center, Research Institute for Ophthalmology and Vision Science, Shahid Beheshti University of Medical Sciences, Tehran, IranStevens-Johnson syndrome (SJS) is a life-threatening mucocutaneous disease with various etiologies including drugs, infections, and malignancies. Ocular manifestations of SJS vary from the membrane, symblepharon formation, and epithelial defect in the acute phase to trichiasis, eyelid margin keratinization, and lacrimal duct obstruction in the chronic phase. A 13-year-old boy with a history of drug-induced SJS presented to our clinic complaining of a mass in the nasal side and inferior fornix of the right eye from 1 year ago. The mass-like lesion in the medial side of the right eye was accompanied by ankyloblepharon, symblepharon, and ptosis and limited ocular movement. Orbital imaging showed cystic lesions on the medial side of the right globe and the inferior fornix. Two large cysts were entirely surgically excised. Histopathologic investigation revealed conjunctival tissue with nonkeratinized epithelium and goblet cells. There was no sign of conjunctival cyst recurrence or symblepharon formation on the 6th-month follow-up. The inferior fornix achieved acceptable depth and the ocular movements became normal.https://beta.karger.com/Article/FullText/533648stevens-johnson syndromeconjunctival cystscase report
spellingShingle Sadid Hooshmandi
Kiana Hassanpour
Amirreza Veisi
Vahid Movafaghi
Farideh Langari
Mohammad-Mehdi Sadoughi
Mohammad Ali Javadi
Management of Large Conjunctival Cysts in a Patient with Stevens-Johnson Syndrome: A Case Report and Review of the Literature
Case Reports in Ophthalmology
stevens-johnson syndrome
conjunctival cysts
case report
title Management of Large Conjunctival Cysts in a Patient with Stevens-Johnson Syndrome: A Case Report and Review of the Literature
title_full Management of Large Conjunctival Cysts in a Patient with Stevens-Johnson Syndrome: A Case Report and Review of the Literature
title_fullStr Management of Large Conjunctival Cysts in a Patient with Stevens-Johnson Syndrome: A Case Report and Review of the Literature
title_full_unstemmed Management of Large Conjunctival Cysts in a Patient with Stevens-Johnson Syndrome: A Case Report and Review of the Literature
title_short Management of Large Conjunctival Cysts in a Patient with Stevens-Johnson Syndrome: A Case Report and Review of the Literature
title_sort management of large conjunctival cysts in a patient with stevens johnson syndrome a case report and review of the literature
topic stevens-johnson syndrome
conjunctival cysts
case report
url https://beta.karger.com/Article/FullText/533648
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