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. 2021 Sep 14;11:18227. doi: 10.1038/s41598-021-97771-w

Figure 2.

Figure 2

(A, B) Example of a 70-year-old female reticular pseudodrusen (RPD) patient that developed a significant increase in RPD-affected area over the 5-year follow-up yet no late-stage form of age-related macular degeneration. (A) Baseline. Above near-infrared confocal scanning laser ophthalmoscopy (cSLO) image showing hyporeflective dots superiorly located to the fovea. Rectangle marks the area magnified below. Grey dotted line marks the location of the optical coherence tomography (OCT) scan below. (B) Same eye after 5 years. Note the increase in RPD-affected area and the increase in lesion density visible both in the cSLO en-face image above as well as in the magnified image. The OCT scans reveal early RPD stages at baseline and predominantly stage-three RPD lesions at 5-year follow-up. Also note signs of incomplete outer retinal atrophy in (B). There is detritus on the intact RPE monolayer with remnants of the ellipsoid zone but no hypertransmission. Individual RPD lesions are harder to discern. (C, D) Example of a 71-year-old female RPD patient that developed geographic atrophy over the 5-year follow-up. (C) Baseline. (D) Same eye after 5 years. Note the perifoveal patches of geographic atrophy and a moderate increase in RPD-affected area and lesion density. The OCT scan appears rather similar to the baseline image without any signs of outer retinal atrophy.