Fig. 1.

Case of initial-onset Vogt–Koyanagi–Harada (VKH) disease at presentation. Indocyanine green angiography (ICGA) performed about 10 days after the onset of symptoms showing numerous hypofluorescent dark dots (HDDs) and severe choroidal vasculitis (fuzzy unrecognizable choroidal vessels) (ICGA score = 31)³⁶(1a). Many posterior pole HDDs and ICGA disc hyperfluorescence indicating severe choroidal inflammation (1b). Fluorescein angiography disc hyperfluorescence (1c). Three weeks after combined systemic corticosteroid and cyclosporine therapy, choroidal vessels have a normal pattern, and HDDs have decreased substantially (ICGA score = 6) (1d). In the posterior pole, HDDs are only faintly noted, and disc ICGA hyperfluorescence has disappeared (1e).