“…Several reports have shown that ICGA revealed choroidal lesions that were not detected by ophthalmoscopy or FA in patients with a variety of chorioretinal inflammatory disorders, including ocular sarcoidosis [4,5], ocular tuberculosis [6], ocular syphilis [7], ocular toxoplasmosis [8][9][10], sympathetic ophthalmia [11], Vogt-Koyanagi-Harada (VKH) disease [12], multifocal choroiditis [13][14][15], acute posterior multifocal placoid pigment epitheliopathy (APMPPE) [13,16], multiple evanescent white dot syndrome (MEWDS) [13,17,18], serpiginous choroiditis [19,20], the choroidal involvement in birdshot chorioretinopathy [21], and lupus choroidopathy [22][23][24]. The use of ICGA has also made it possible to better understand the pathogenesis of several choroidal inflammatory disorders and to classify these entities based on either predominant inflammation of the choriocapillaris or predominant inflammation of the stromal choroidal vessels with or without secondary choriocapillaritis [25].…”