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Kayser–Fleischer ring with keratoconus: a coincidence? A case report
BACKGROUND: It is rare for hepatolenticular degeneration [Wilson’s disease (WD)] to occur along with keratoconus (KC). In our report, a teenager was diagnosed with WD because of the discovery of Kayser–Fleischer (KF) ring in the cornea, and concomitant KC was found. CASE PRESENTATION: A 19-year-old...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7222518/ https://www.ncbi.nlm.nih.gov/pubmed/32404122 http://dx.doi.org/10.1186/s12886-020-01463-4 |
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author | Hu, Peike Lin, Lin Wu, Zhiyi Jin, Xiuming Ni, Hailong |
author_facet | Hu, Peike Lin, Lin Wu, Zhiyi Jin, Xiuming Ni, Hailong |
author_sort | Hu, Peike |
collection | PubMed |
description | BACKGROUND: It is rare for hepatolenticular degeneration [Wilson’s disease (WD)] to occur along with keratoconus (KC). In our report, a teenager was diagnosed with WD because of the discovery of Kayser–Fleischer (KF) ring in the cornea, and concomitant KC was found. CASE PRESENTATION: A 19-year-old male was diagnosed with KC due to a rapid decline in visual acuity within a short period of time. Ocular examination revealed the presence of ring-shaped, dense, brown sediment at the Descemet membrane of the bilateral limbus cornea, exhibiting characteristics similar to those of KF ring. Then, the patient was referred to the Department of Neurology and diagnosed with asymptomatic WD. During the next 5 years of follow-up, the patient has worn RGP lenses, routinely taken drugs that inhibit copper absorption and promote copper excretion, and maintained a low-copper diet. He has never exhibited obvious systemic symptoms associated with WD, such as neurological, mental, or hepatic dysfunction, and the color of the KF ring has grown obviously lighter. Moreover, the morphology of the cornea has stabilized. CONCLUSION: Only one report of WD combined with KC was found in the literature. So far, there is no evidence of a correlation between the occurrence of the two diseases. However, a low-copper diet and active copper-reducing therapy may have played a role in stabilizing the patient’s condition in this case. |
format | Online Article Text |
id | pubmed-7222518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72225182020-05-20 Kayser–Fleischer ring with keratoconus: a coincidence? A case report Hu, Peike Lin, Lin Wu, Zhiyi Jin, Xiuming Ni, Hailong BMC Ophthalmol Case Report BACKGROUND: It is rare for hepatolenticular degeneration [Wilson’s disease (WD)] to occur along with keratoconus (KC). In our report, a teenager was diagnosed with WD because of the discovery of Kayser–Fleischer (KF) ring in the cornea, and concomitant KC was found. CASE PRESENTATION: A 19-year-old male was diagnosed with KC due to a rapid decline in visual acuity within a short period of time. Ocular examination revealed the presence of ring-shaped, dense, brown sediment at the Descemet membrane of the bilateral limbus cornea, exhibiting characteristics similar to those of KF ring. Then, the patient was referred to the Department of Neurology and diagnosed with asymptomatic WD. During the next 5 years of follow-up, the patient has worn RGP lenses, routinely taken drugs that inhibit copper absorption and promote copper excretion, and maintained a low-copper diet. He has never exhibited obvious systemic symptoms associated with WD, such as neurological, mental, or hepatic dysfunction, and the color of the KF ring has grown obviously lighter. Moreover, the morphology of the cornea has stabilized. CONCLUSION: Only one report of WD combined with KC was found in the literature. So far, there is no evidence of a correlation between the occurrence of the two diseases. However, a low-copper diet and active copper-reducing therapy may have played a role in stabilizing the patient’s condition in this case. BioMed Central 2020-05-13 /pmc/articles/PMC7222518/ /pubmed/32404122 http://dx.doi.org/10.1186/s12886-020-01463-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Hu, Peike Lin, Lin Wu, Zhiyi Jin, Xiuming Ni, Hailong Kayser–Fleischer ring with keratoconus: a coincidence? A case report |
title | Kayser–Fleischer ring with keratoconus: a coincidence? A case report |
title_full | Kayser–Fleischer ring with keratoconus: a coincidence? A case report |
title_fullStr | Kayser–Fleischer ring with keratoconus: a coincidence? A case report |
title_full_unstemmed | Kayser–Fleischer ring with keratoconus: a coincidence? A case report |
title_short | Kayser–Fleischer ring with keratoconus: a coincidence? A case report |
title_sort | kayser–fleischer ring with keratoconus: a coincidence? a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7222518/ https://www.ncbi.nlm.nih.gov/pubmed/32404122 http://dx.doi.org/10.1186/s12886-020-01463-4 |
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