Vogt-Koyanagi-Harada (VKH) disease is a multisystem autoimmune disorder involving the eyes, ears, meninges, and skin. Ophthalmological hallmarks are bilateral panuveitis and serous retinal detachments.1 Histologically, the disease is characterized by inflammation of the choroid.2 We present a case that provides unique insights owing to the direct correlation of multimodal clinical imaging with histology.
Patrick Oellers, Glenn J. Jaffe, Alan D. Proia. Clinical-Pathological Correlation of Vogt-Koyanagi-Harada Disease. JAMA Ophthalmol. 2016;134(3):343–345. doi:10.1001/jamaophthalmol.2015.5464