Skip to main content
Fig. 3 | Journal of Ophthalmic Inflammation and Infection

Fig. 3

From: Acute macular neuroretinopathy with coexistent central retinal vein occlusion as the presenting feature in intraocular tuberculosis

Fig. 3

Multimodal imaging findings revealing the presence of retinal and choroidal granulomas and peripapillary choroidal neovascular membrane (CNV). a The pseudocolour image with Optos, Daytona shows a grey-white lesion superotemporal to the optic nerve head (yellow solid arrow) and subtle elevated lesion nasal to the optic disc and temporal to the macula (white hollow arrows) suggestive of choroidal granulomas. b Horizontal line scan through the middle portion of the optic disc reveals the presence of peripapillary, subretinal choroidal neovascular membrane (blue solid arrow). c Horizontal line scan through the retina superior to the optic disc shows the presence of granuloma within the retinal layers (yellow solid arrow) and associated subretinal fluid. d–f Progressive phases of combined fluorescein (FA) and indocyanine green angiography (ICGA) of the left eye. The retinal granuloma, seen superotemporal to the optic nerve head, shows hypofluorescence in early phase with increasing hyperfluoroscence in the late phases of the FA (yellow solid arrow). On the ICGA, the lesion shows early hypofluorescence with mild staining of the lesion in the late phases (yellow solid arrow). The choroidal granulomas are not identified on the FA. The choroidal granulomas are seen on the ICGA as early hypofluorescent lesions with staining in the late phases (white arrow). The middle portion of the optic nerve head identifies a mild hyper fluorescent lesion in the early phase of the FA which increases in intensity and size in the late phases suggestive of peripapillary CNV (blue solid arrow). Capillary non-perfusion areas are not visualised on FA. On the ICGA, the neovascular complex involving the optic nerve head is well delineated (blue solid arrow)

Back to article page