Case Report: Case of Bilateral Panuveitis Due to Probable Vogt Koyanagi Harada Disease
Abstract: The rare multisystem inflammatory disease known as Vogt - Koyanagi - Harada syndrome is typified by panuveitis with serous retinal detachment. It is frequently linked to cutaneous and neurologic symptoms such as vitiligo, headache, hearing loss, and poliosis. A widespread autoimmune reaction against melanocyte - associated antigens that begins in the choroidal stroma causes VKH illness. Although it is always bilateral, it might be asymmetrical. We are presenting a case report of 33years old female with painless diminution of vision and associated with headache since 15days. On slit lamp examination, Conjunctival congestion and cells present. Fundus examination showed, bilateral multifocal exudative retinal detachment and hyperemic and edematous disc. B scan examination revealed multifocal serous retinal detachment. On fundus fluorescein angiography, multiple pinpoint foci giving a starry sky appearance is seen.
Keywords: Vogt Koyanagi harada, Exudative retinal detachment, Pan uveitis
How to Cite?: Dr. Shaik Shaheen, Dr. Nameet D Souza, Dr. Shamantha MC, "Case Report: Case of Bilateral Panuveitis Due to Probable Vogt Koyanagi Harada Disease", Volume 14 Issue 7, July 2025, International Journal of Science and Research (IJSR), Pages: 508-511, https://www.ijsr.net/getabstract.php?paperid=SR25628100412, DOI: https://dx.doi.org/10.21275/SR25628100412