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. 2020 Jun 29;9(7):2034. doi: 10.3390/jcm9072034

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© 2020 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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Typical images of pachychoroid neovasculopathy (modified from [149]). Color fundus photography reveals an orange-red nodular lesion, serous retinal detachment, and hard exudates (A). Fluorescein angiography reveals a window defect corresponding to RPE atrophy and occult choroidal neovascularization (B). Indocyanine green angiography shows choroidal neovascularization and some polypoidal lesions (C). A vertical optical coherence tomography (OCT) scan through the fovea shows subretinal fluid and protrusion of retinal pigment epithelium resulting from polypoidal lesions (D). A horizontal enhanced depth imaging OCT scan through the fovea shows thickened subfoveal choroidal thickness (triangles) and pachyvessels (asterisks) (E).