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Monocular posterior scleritis presenting as acute conjunctivitis: A case report

BACKGROUND: Posterior scleritis is a rare inflammatory ocular disease, characterized by severe and painful inflammation of the sclera. It is often misdiagnosed or underdiagnosed, due to its general and varying clinical presentation profile, which primarily involves pain and visual impairment but whi...

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Autores principales: Li, Yan-Zhen, Qin, Xiu-Hong, Lu, Jian-Min, Wang, Yong-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642562/
https://www.ncbi.nlm.nih.gov/pubmed/33195678
http://dx.doi.org/10.12998/wjcc.v8.i20.5030
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author Li, Yan-Zhen
Qin, Xiu-Hong
Lu, Jian-Min
Wang, Yong-Ping
author_facet Li, Yan-Zhen
Qin, Xiu-Hong
Lu, Jian-Min
Wang, Yong-Ping
author_sort Li, Yan-Zhen
collection PubMed
description BACKGROUND: Posterior scleritis is a rare inflammatory ocular disease, characterized by severe and painful inflammation of the sclera. It is often misdiagnosed or underdiagnosed, due to its general and varying clinical presentation profile, which primarily involves pain and visual impairment but which can include eyelid edema, choroidal folds, serous retinal detachment, disc edema, hard exudates in fovea and subretinal mass. We report here a case of posterior scleritis, with symptoms of eye pain and red eye, initially misdiagnosed as acute conjunctivitis. CASE SUMMARY: A 56-year-old man presented to a local hospital with complaint of pain and redness in the right eye. The initial diagnosis was acute conjunctivitis and he was given antibiotic eyedrops. Upon week-long continuance of the symptoms despite treatment, he presented to our hospital. Initial examination revealed a shallow anterior chamber in the right eye and vision reduction to 0.6. Further testing by optical coherence tomography, ultrasound biomicroscopy, and fundus photography indicated diagnosis of posterior scleritis. The patient was given methylprednisolone (oral) on a tapered reduction schedule (starting with 70 mg/d). According to the peaks and troughs of symptoms, compound betamethasone injection was administered into the bulb, culminating in discontinuation of the oral corticosteroid. Subsequent optical coherence tomography showed the subretinal fluid near the optic disc to be completely absorbed after treatment. CONCLUSION: Posterior scleritis should be among the differential diagnosis of eye pain and redness, and diagnosis requires further ophthalmic accessory examination, such as by optical coherence tomography.
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spelling pubmed-76425622020-11-13 Monocular posterior scleritis presenting as acute conjunctivitis: A case report Li, Yan-Zhen Qin, Xiu-Hong Lu, Jian-Min Wang, Yong-Ping World J Clin Cases Case Report BACKGROUND: Posterior scleritis is a rare inflammatory ocular disease, characterized by severe and painful inflammation of the sclera. It is often misdiagnosed or underdiagnosed, due to its general and varying clinical presentation profile, which primarily involves pain and visual impairment but which can include eyelid edema, choroidal folds, serous retinal detachment, disc edema, hard exudates in fovea and subretinal mass. We report here a case of posterior scleritis, with symptoms of eye pain and red eye, initially misdiagnosed as acute conjunctivitis. CASE SUMMARY: A 56-year-old man presented to a local hospital with complaint of pain and redness in the right eye. The initial diagnosis was acute conjunctivitis and he was given antibiotic eyedrops. Upon week-long continuance of the symptoms despite treatment, he presented to our hospital. Initial examination revealed a shallow anterior chamber in the right eye and vision reduction to 0.6. Further testing by optical coherence tomography, ultrasound biomicroscopy, and fundus photography indicated diagnosis of posterior scleritis. The patient was given methylprednisolone (oral) on a tapered reduction schedule (starting with 70 mg/d). According to the peaks and troughs of symptoms, compound betamethasone injection was administered into the bulb, culminating in discontinuation of the oral corticosteroid. Subsequent optical coherence tomography showed the subretinal fluid near the optic disc to be completely absorbed after treatment. CONCLUSION: Posterior scleritis should be among the differential diagnosis of eye pain and redness, and diagnosis requires further ophthalmic accessory examination, such as by optical coherence tomography. Baishideng Publishing Group Inc 2020-10-26 2020-10-26 /pmc/articles/PMC7642562/ /pubmed/33195678 http://dx.doi.org/10.12998/wjcc.v8.i20.5030 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Report
Li, Yan-Zhen
Qin, Xiu-Hong
Lu, Jian-Min
Wang, Yong-Ping
Monocular posterior scleritis presenting as acute conjunctivitis: A case report
title Monocular posterior scleritis presenting as acute conjunctivitis: A case report
title_full Monocular posterior scleritis presenting as acute conjunctivitis: A case report
title_fullStr Monocular posterior scleritis presenting as acute conjunctivitis: A case report
title_full_unstemmed Monocular posterior scleritis presenting as acute conjunctivitis: A case report
title_short Monocular posterior scleritis presenting as acute conjunctivitis: A case report
title_sort monocular posterior scleritis presenting as acute conjunctivitis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642562/
https://www.ncbi.nlm.nih.gov/pubmed/33195678
http://dx.doi.org/10.12998/wjcc.v8.i20.5030
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