“…Other important clinical manifestations of the pachychoroid spectrum disease, besides FCE and CSC, are pachychoroid pigment epitheliopathy, pachychoroid neovasculopathy, polypoidal choroidal vasculopathy/aneurysmal type 1 neovascularization, and peripapillary pachychoroid syndrome (11) . In addition to FA and ICGA, other imaging features allow better characterization of the FCE: i) optical coherence tomography (OCT) may reveal high hyperreflective choroidal thinning in the area of the FCE, a separation or attachment between photoreceptors and the retinal pigment epithelium (RPE), and absence of abnormalities of the underlying sclera (11) ; ii) swept-source, enhanced depth imaging, and three-dimensional OCT can improve choroid and sclera analysis (2,4,12) ; iii) OCT angiography may demonstrate alteration of the deep capillary and choriocapillaris plexus (13) .…”