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Bilateral retrocorneal hyaline scrolls secondary to asymptomatic congenital syphilis: A case report
BACKGROUND: Retrocorneal hyaline scrolls are a rare phenomenon. We report a case of bilateral retrocorneal hyaline scrolls that were likely induced by asymptomatic congenital syphilis. CASE SUMMARY: A 71-year-old woman presented with blurred vision due to cataracts. Slit-lamp microscopy revealed bil...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8026840/ https://www.ncbi.nlm.nih.gov/pubmed/33869603 http://dx.doi.org/10.12998/wjcc.v9.i10.2274 |
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author | Jin, Yu-Qi Hu, Yong-Ping Dai, Qi Wu, Shuang-Qing |
author_facet | Jin, Yu-Qi Hu, Yong-Ping Dai, Qi Wu, Shuang-Qing |
author_sort | Jin, Yu-Qi |
collection | PubMed |
description | BACKGROUND: Retrocorneal hyaline scrolls are a rare phenomenon. We report a case of bilateral retrocorneal hyaline scrolls that were likely induced by asymptomatic congenital syphilis. CASE SUMMARY: A 71-year-old woman presented with blurred vision due to cataracts. Slit-lamp microscopy revealed bilateral hyaline scrolls with a dichotomous branching pattern extending to the anterior chamber or rods attaching to the rough posterior surface of the cornea. The patient was positive for syphilis-specific antibodies, with no ocular or systemic evidence of congenital or acquired syphilis. Binocular cataract, retrocorneal scroll, and corneal endothelial gutta were considered. The scroll of the right eye was removed during cataract surgery and further observed using hematoxylin–eosin staining and scanning electron microscopy. The cornea of the right eye remained transparent, and the residual scroll seemed stable, however, the corneal endothelial density declined at 13 mo after surgery. In vivo confocal microscopy revealed coalescence of corneal guttae at the level of the corneal endothelium or adhesion to the posterior surface of the endothelium, with enlarged endothelial cells in both eyes. Activated keratocytes in the stroma and a highly reflective acellular structure at the level of the Descemet’s membrane were observed. The removed scroll had a cartilage-like hardness and a circularly arranged fiber-like acellular structure. CONCLUSION: Occult congenital syphilis could induce corneal endothelial gutta and the formation of retrocorneal scrolls without other signs of ocular syphilis. |
format | Online Article Text |
id | pubmed-8026840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-80268402021-04-16 Bilateral retrocorneal hyaline scrolls secondary to asymptomatic congenital syphilis: A case report Jin, Yu-Qi Hu, Yong-Ping Dai, Qi Wu, Shuang-Qing World J Clin Cases Case Report BACKGROUND: Retrocorneal hyaline scrolls are a rare phenomenon. We report a case of bilateral retrocorneal hyaline scrolls that were likely induced by asymptomatic congenital syphilis. CASE SUMMARY: A 71-year-old woman presented with blurred vision due to cataracts. Slit-lamp microscopy revealed bilateral hyaline scrolls with a dichotomous branching pattern extending to the anterior chamber or rods attaching to the rough posterior surface of the cornea. The patient was positive for syphilis-specific antibodies, with no ocular or systemic evidence of congenital or acquired syphilis. Binocular cataract, retrocorneal scroll, and corneal endothelial gutta were considered. The scroll of the right eye was removed during cataract surgery and further observed using hematoxylin–eosin staining and scanning electron microscopy. The cornea of the right eye remained transparent, and the residual scroll seemed stable, however, the corneal endothelial density declined at 13 mo after surgery. In vivo confocal microscopy revealed coalescence of corneal guttae at the level of the corneal endothelium or adhesion to the posterior surface of the endothelium, with enlarged endothelial cells in both eyes. Activated keratocytes in the stroma and a highly reflective acellular structure at the level of the Descemet’s membrane were observed. The removed scroll had a cartilage-like hardness and a circularly arranged fiber-like acellular structure. CONCLUSION: Occult congenital syphilis could induce corneal endothelial gutta and the formation of retrocorneal scrolls without other signs of ocular syphilis. Baishideng Publishing Group Inc 2021-04-06 2021-04-06 /pmc/articles/PMC8026840/ /pubmed/33869603 http://dx.doi.org/10.12998/wjcc.v9.i10.2274 Text en ©The Author(s) 2021. 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. |
spellingShingle | Case Report Jin, Yu-Qi Hu, Yong-Ping Dai, Qi Wu, Shuang-Qing Bilateral retrocorneal hyaline scrolls secondary to asymptomatic congenital syphilis: A case report |
title | Bilateral retrocorneal hyaline scrolls secondary to asymptomatic congenital syphilis: A case report |
title_full | Bilateral retrocorneal hyaline scrolls secondary to asymptomatic congenital syphilis: A case report |
title_fullStr | Bilateral retrocorneal hyaline scrolls secondary to asymptomatic congenital syphilis: A case report |
title_full_unstemmed | Bilateral retrocorneal hyaline scrolls secondary to asymptomatic congenital syphilis: A case report |
title_short | Bilateral retrocorneal hyaline scrolls secondary to asymptomatic congenital syphilis: A case report |
title_sort | bilateral retrocorneal hyaline scrolls secondary to asymptomatic congenital syphilis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8026840/ https://www.ncbi.nlm.nih.gov/pubmed/33869603 http://dx.doi.org/10.12998/wjcc.v9.i10.2274 |
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