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Vogt-Koyanagi-Harada disease following influenza vaccination
PURPOSE: To report a case of Vogt–Koyanagi–Harada (VKH) disease following influenza vaccination. OBSERVATIONS: A 30-year-old Filipino male developed bilateral pain, redness, photophobia, floaters, headache and tinnitus 2 days after receiving the annual influenza vaccine. He presented to the emergenc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020092/ https://www.ncbi.nlm.nih.gov/pubmed/35464684 http://dx.doi.org/10.1016/j.ajoc.2022.101516 |
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author | Murtaza, Fahmeeda Pereira, Austin Mandelcorn, Mark S. Kaplan, Alexander J. |
author_facet | Murtaza, Fahmeeda Pereira, Austin Mandelcorn, Mark S. Kaplan, Alexander J. |
author_sort | Murtaza, Fahmeeda |
collection | PubMed |
description | PURPOSE: To report a case of Vogt–Koyanagi–Harada (VKH) disease following influenza vaccination. OBSERVATIONS: A 30-year-old Filipino male developed bilateral pain, redness, photophobia, floaters, headache and tinnitus 2 days after receiving the annual influenza vaccine. He presented to the emergency department 5 days after symptom onset. His past medical and ocular history was unremarkable. His best-corrected distance visual acuity (BCVA) was 20/100 in the right eye (OD) and 20/150 in the left eye (OS). Slit-lamp examination revealed fine keratic precipitates and 1+ anterior chamber cells in both eyes (OU). Dilated fundus examination revealed 1+ vitreous cells with trace haze and multiple serous retinal detachments OU. Magnetic resonance imaging (MRI) of the brain and chest X-ray were unremarkable. Serologic testing was negative for infectious, inflammatory and neoplastic causes. The patient tested positive for HLA-DR4. A diagnosis of acute Vogt-Koyanagi-Harada disease was made and high-dose oral prednisone, intravitreal triamcinolone acetonide and mycophenolate mofetil were needed to achieve quiescence. At 6 months follow-up, our patient remains in remission with no active intraocular inflammation or subretinal fluid. His BCVA has improved to 20/50 OD and 20/30 OS. CONCLUSION AND IMPORTANCE: The annual influenza vaccine may be a trigger for onset or recurrence of VKH in genetically susceptible individuals. |
format | Online Article Text |
id | pubmed-9020092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90200922022-04-21 Vogt-Koyanagi-Harada disease following influenza vaccination Murtaza, Fahmeeda Pereira, Austin Mandelcorn, Mark S. Kaplan, Alexander J. Am J Ophthalmol Case Rep Case Report PURPOSE: To report a case of Vogt–Koyanagi–Harada (VKH) disease following influenza vaccination. OBSERVATIONS: A 30-year-old Filipino male developed bilateral pain, redness, photophobia, floaters, headache and tinnitus 2 days after receiving the annual influenza vaccine. He presented to the emergency department 5 days after symptom onset. His past medical and ocular history was unremarkable. His best-corrected distance visual acuity (BCVA) was 20/100 in the right eye (OD) and 20/150 in the left eye (OS). Slit-lamp examination revealed fine keratic precipitates and 1+ anterior chamber cells in both eyes (OU). Dilated fundus examination revealed 1+ vitreous cells with trace haze and multiple serous retinal detachments OU. Magnetic resonance imaging (MRI) of the brain and chest X-ray were unremarkable. Serologic testing was negative for infectious, inflammatory and neoplastic causes. The patient tested positive for HLA-DR4. A diagnosis of acute Vogt-Koyanagi-Harada disease was made and high-dose oral prednisone, intravitreal triamcinolone acetonide and mycophenolate mofetil were needed to achieve quiescence. At 6 months follow-up, our patient remains in remission with no active intraocular inflammation or subretinal fluid. His BCVA has improved to 20/50 OD and 20/30 OS. CONCLUSION AND IMPORTANCE: The annual influenza vaccine may be a trigger for onset or recurrence of VKH in genetically susceptible individuals. Elsevier 2022-04-10 /pmc/articles/PMC9020092/ /pubmed/35464684 http://dx.doi.org/10.1016/j.ajoc.2022.101516 Text en © 2022 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Murtaza, Fahmeeda Pereira, Austin Mandelcorn, Mark S. Kaplan, Alexander J. Vogt-Koyanagi-Harada disease following influenza vaccination |
title | Vogt-Koyanagi-Harada disease following influenza vaccination |
title_full | Vogt-Koyanagi-Harada disease following influenza vaccination |
title_fullStr | Vogt-Koyanagi-Harada disease following influenza vaccination |
title_full_unstemmed | Vogt-Koyanagi-Harada disease following influenza vaccination |
title_short | Vogt-Koyanagi-Harada disease following influenza vaccination |
title_sort | vogt-koyanagi-harada disease following influenza vaccination |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020092/ https://www.ncbi.nlm.nih.gov/pubmed/35464684 http://dx.doi.org/10.1016/j.ajoc.2022.101516 |
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