Fig. 3.

Follow-up of a case of initial-onset Vogt–Koyanagi–Harada (VKH) disease monitored by enhanced depth imaging optical coherence tomography (EDI-OCT) (average thickness indicated in yellow on scans). Three weeks after aggressive corticosteroid and cyclosporine therapy, there was a decrease of choroidal thickness from 550 to 375 μm with remaining pouches of subretinal fluid (3a). After that, EDI-OCT was unable to detect subclinical recurrences and their resolution seen by Indocyanine green angiography (ICGA) (3b-3f), although the choroidal thickness is gradually decreasing over time to 283 μm (3g).