“…Despite being able to distinguish lesions from normal tissue, the low penetration capability of OCT limits its usage to only very thin lesions, typically less than 1 mm in thickness, especially in melanocytic lesions [ 11 ], whereas choroidal tumors can have a height of up to 10 mm [ 12 ]. Imaging techniques such as fluorescein angiography (FA), indocyanine green angiography (ICGA), and fundus autofluorescence (FAF) can provide valuable information such as changes in the retinal pigmented epithelium (RPE) overlying ocular lesions, tumor vasculature, and associated vascular leakage [ 1 , 2 , 13 , 14 ]. However, these imaging modalities do not provide sufficient information related to tumor depth, and their standalone diagnostic accuracy is relatively low.…”