Fig. 2
From: Multi-modal imaging and anatomic classification of the white dot syndromes
Punctate inner choroidopathy (PIC). A 43-year-old myopic woman presented with bilateral multifocal lesions (a–b). Fluorescein angiography (FA) showed blockage and mild rims of hyperfluorescence in earlier frames (c, e), which stained over time (g, i). Indocyanine green (ICG) showed similar patterns but more hypocyanescent overall (d, h, f, j). Fundus autofluorescence demonstrated hypoautofluorescence of the lesions seen on FA and ICG (k, m). Infrared imaging showed hyperreflectance of the lesions (o, q). Spectral-domain optical coherence tomography through the fovea of the right eye was normal (l), but the B-scans through the lesion superior to the fovea revealed disruption of the outer retina and retinal pigment epithelium (p). Similar lesions were noted in the left eye (n, r)