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Hammered silver appearance of the corneal endothelium in Fuchs uveitis syndrome: A case report
BACKGROUND: Hammered silver appearance of the corneal endothelium is considered a characteristic change in iridocorneal-endothelial syndrome. Herein we report an interesting case of hammered silver appearance of the corneal endothelium in Fuchs uveitis syndrome (FUS). CASE SUMMARY: A 49-year-old man...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782945/ https://www.ncbi.nlm.nih.gov/pubmed/36568999 http://dx.doi.org/10.12998/wjcc.v10.i35.13081 |
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author | Cheng, Yan-Yan Wang, Cong-Ying Zheng, Yan-Fang Ren, Ming-Yu |
author_facet | Cheng, Yan-Yan Wang, Cong-Ying Zheng, Yan-Fang Ren, Ming-Yu |
author_sort | Cheng, Yan-Yan |
collection | PubMed |
description | BACKGROUND: Hammered silver appearance of the corneal endothelium is considered a characteristic change in iridocorneal-endothelial syndrome. Herein we report an interesting case of hammered silver appearance of the corneal endothelium in Fuchs uveitis syndrome (FUS). CASE SUMMARY: A 49-year-old man with progressive vision loss in the right eye for one year was admitted to our hospital. The clinical manifestations of the patient’s right eye were mild conjunctival hyperemia, scattered stellate keratic precipitates on the corneal endothelium, normal depth anterior chamber, 2+ cellular reaction in the aqueous humor, diffuse iris depigmentation, absence of synechia, Koeppe nodules, opalescent lens, and vitreous opacity. FUS and a complicated cataract were diagnosed based on the typical clinical manifestations. The corneal endothelial changes were recorded in detail by slit-lamp examination, specular microscopy, and in vivo confocal microscopy before cataract extraction, revealing a hammered silver appearance of the corneal endothelium in the affected eye, a wide-band dark area, as well as irregular corneal endothelial protuberances and dark bodies of various sizes. Subsequently, the patient underwent phacoemulsification combined with intraocular lens implantation, and his postoperative visual acuity recovered to 1.0. CONCLUSION: Hammered silver appearance of the corneal endothelium in FUS, which is considered a more serious manifestation of endothelial damage, is rare and may be caused by many irregular protrusions in the corneal endothelium. |
format | Online Article Text |
id | pubmed-9782945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-97829452022-12-24 Hammered silver appearance of the corneal endothelium in Fuchs uveitis syndrome: A case report Cheng, Yan-Yan Wang, Cong-Ying Zheng, Yan-Fang Ren, Ming-Yu World J Clin Cases Case Report BACKGROUND: Hammered silver appearance of the corneal endothelium is considered a characteristic change in iridocorneal-endothelial syndrome. Herein we report an interesting case of hammered silver appearance of the corneal endothelium in Fuchs uveitis syndrome (FUS). CASE SUMMARY: A 49-year-old man with progressive vision loss in the right eye for one year was admitted to our hospital. The clinical manifestations of the patient’s right eye were mild conjunctival hyperemia, scattered stellate keratic precipitates on the corneal endothelium, normal depth anterior chamber, 2+ cellular reaction in the aqueous humor, diffuse iris depigmentation, absence of synechia, Koeppe nodules, opalescent lens, and vitreous opacity. FUS and a complicated cataract were diagnosed based on the typical clinical manifestations. The corneal endothelial changes were recorded in detail by slit-lamp examination, specular microscopy, and in vivo confocal microscopy before cataract extraction, revealing a hammered silver appearance of the corneal endothelium in the affected eye, a wide-band dark area, as well as irregular corneal endothelial protuberances and dark bodies of various sizes. Subsequently, the patient underwent phacoemulsification combined with intraocular lens implantation, and his postoperative visual acuity recovered to 1.0. CONCLUSION: Hammered silver appearance of the corneal endothelium in FUS, which is considered a more serious manifestation of endothelial damage, is rare and may be caused by many irregular protrusions in the corneal endothelium. Baishideng Publishing Group Inc 2022-12-16 2022-12-16 /pmc/articles/PMC9782945/ /pubmed/36568999 http://dx.doi.org/10.12998/wjcc.v10.i35.13081 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (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. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Case Report Cheng, Yan-Yan Wang, Cong-Ying Zheng, Yan-Fang Ren, Ming-Yu Hammered silver appearance of the corneal endothelium in Fuchs uveitis syndrome: A case report |
title | Hammered silver appearance of the corneal endothelium in Fuchs uveitis syndrome: A case report |
title_full | Hammered silver appearance of the corneal endothelium in Fuchs uveitis syndrome: A case report |
title_fullStr | Hammered silver appearance of the corneal endothelium in Fuchs uveitis syndrome: A case report |
title_full_unstemmed | Hammered silver appearance of the corneal endothelium in Fuchs uveitis syndrome: A case report |
title_short | Hammered silver appearance of the corneal endothelium in Fuchs uveitis syndrome: A case report |
title_sort | hammered silver appearance of the corneal endothelium in fuchs uveitis syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782945/ https://www.ncbi.nlm.nih.gov/pubmed/36568999 http://dx.doi.org/10.12998/wjcc.v10.i35.13081 |
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