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Vogt–Koyanagi–Harada syndrome in the setting of COVID‐19 infection
To report a case of Vogt–Koyanagi–Harada disease (VKH) in a 27‐year‐old male 2 weeks proceeding COVID‐19 infection onset. Severe complications of VKH can be avoided by early diagnosis and adequate treatment with corticosteroids and immunosuppressants. It is possible that COVID‐19 was a potential imm...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025255/ https://www.ncbi.nlm.nih.gov/pubmed/36950665 http://dx.doi.org/10.1002/ccr3.6617 |
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author | Eatz, Tiffany Charles, Jude Hassan |
author_facet | Eatz, Tiffany Charles, Jude Hassan |
author_sort | Eatz, Tiffany |
collection | PubMed |
description | To report a case of Vogt–Koyanagi–Harada disease (VKH) in a 27‐year‐old male 2 weeks proceeding COVID‐19 infection onset. Severe complications of VKH can be avoided by early diagnosis and adequate treatment with corticosteroids and immunosuppressants. It is possible that COVID‐19 was a potential immunological trigger of VKH in our patient. |
format | Online Article Text |
id | pubmed-10025255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100252552023-03-21 Vogt–Koyanagi–Harada syndrome in the setting of COVID‐19 infection Eatz, Tiffany Charles, Jude Hassan Clin Case Rep Case Report To report a case of Vogt–Koyanagi–Harada disease (VKH) in a 27‐year‐old male 2 weeks proceeding COVID‐19 infection onset. Severe complications of VKH can be avoided by early diagnosis and adequate treatment with corticosteroids and immunosuppressants. It is possible that COVID‐19 was a potential immunological trigger of VKH in our patient. John Wiley and Sons Inc. 2023-03-19 /pmc/articles/PMC10025255/ /pubmed/36950665 http://dx.doi.org/10.1002/ccr3.6617 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Eatz, Tiffany Charles, Jude Hassan Vogt–Koyanagi–Harada syndrome in the setting of COVID‐19 infection |
title |
Vogt–Koyanagi–Harada syndrome in the setting of COVID‐19 infection |
title_full |
Vogt–Koyanagi–Harada syndrome in the setting of COVID‐19 infection |
title_fullStr |
Vogt–Koyanagi–Harada syndrome in the setting of COVID‐19 infection |
title_full_unstemmed |
Vogt–Koyanagi–Harada syndrome in the setting of COVID‐19 infection |
title_short |
Vogt–Koyanagi–Harada syndrome in the setting of COVID‐19 infection |
title_sort | vogt–koyanagi–harada syndrome in the setting of covid‐19 infection |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025255/ https://www.ncbi.nlm.nih.gov/pubmed/36950665 http://dx.doi.org/10.1002/ccr3.6617 |
work_keys_str_mv | AT eatztiffany vogtkoyanagiharadasyndromeinthesettingofcovid19infection AT charlesjudehassan vogtkoyanagiharadasyndromeinthesettingofcovid19infection |