From: Acute posterior multifocal placoid pigment epitheliopathy (APMPPE)
 | FFA | ICGA | FAF | SD-OCT | EDI-OCT | OCT-A | |
---|---|---|---|---|---|---|---|
APMPPE | Active disease | Early hypofluorescence, late hyperfluorescence | Early and late hypofluorescence | Initial hypoautofluorescence, with progressive increase in hyperautofluorescence | Disruption of the outer retinal and ellipsoid zone, with hyperreflective material at the level of the outer retinal layers and RPE | Choroidal thickening | Areas of flow void at the level of the choriocapillaris |
Healed disease | Early and late hyper and hypofluorescence reflecting RPE disturbance (window defect and pigmentary changes) | Normalisation | Mixed pattern of hypoautofluorescence and hyperautofluorescence, followed by homogenous hypoautofluorescent | Either partial restoration of outer retina or focal areas of photoreceptors/RPE atrophy | Normalisation of choroidal thickness | Normalisation of choriocapillaris flow |