PROBABLE VOGT–KOYANAGI–HARADA SYNDROME: A RARE PRESENTATION IN A PAKISTANI MALE

Authors

  • Imran Ahmad a:1:{s:5:"en_US";s:66:"Khyber Medical College Peshawar/ Khyber Teaching Hospital Peshawar";}
  • Asna Tahir
  • Hina Ikhtiyar
  • Muhammad Usman
  • Ansa Anam

Keywords:

opthalmogy

Abstract

A 48-year-old male presented to us as an out-patient with a painless blurring of vision for five days. On examination, the
visual acuity (VA) of his right eye was 6/36, while that of his left eye was 6/24. The rest of the systemic examination showed
no notable findings except for fundus examination, which revealed multiple serous retinal detachments (SRD) confirmed
on Optical Coherence Tomography (OCT). Treatment involved intravenous administration of 1 gram methylprednisolone
followed by oral steroids. His condition significantly improved after three doses with a corresponding enhancement in visual
acuity with a resolution of SRDs. This case report illustrates the efficacy of corticosteroids in the initial and successful treat
ment of Vogt-Koyanagi-Harada syndrome.

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Published

2025-11-18

How to Cite

Ahmad, I., Tahir, A., Ikhtiyar, H., Usman, M., & Anam, A. (2025). PROBABLE VOGT–KOYANAGI–HARADA SYNDROME: A RARE PRESENTATION IN A PAKISTANI MALE. Journal of Medical Sciences, 32(3). Retrieved from https://jmedsci.com/Jmedsci/article/view/1949

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