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Retinal Angiomatous Proliferation Stage 1

Description

Characteristics:

The current classification of neovascular Age-Related Macular Degeneration (AMD) is based on the findings of Optical Coherence Tomography (OCT), which distinguishes 3 types of neovascular membrane, taking as an anatomical reference the line of the Retinal Pigment Epithelium (RPE) and the nature of the neovascular tissue.

Retinal angiomatous proliferation (RAP or AMD type 3) originates in the deep retinal vascular complex and is characterized by the presence of cystoid macular edema, which may develop into serous RPE detachment (PED), associated or not with subretinal fluid. The initial response to antiangiogenic treatment is very good, however, the high risk of development and progression to atrophy means that the long-term prognosis is not as good. Likewise, the high risk of bilaterality makes close monitoring of the contralateral eye necessary in order to make an early diagnosis.

Comments

Indication

A 56-year-old male was diagnosed with exudative neovascular membrane in his right eye that had been developing for years and was being treated on a treat-and-extend basis. During a routine visit, a small intraretinal hemorrhage and intraretinal fluid were detected in the context of soft macular drusen in his left eye. Corrected visual acuity was counting fingers at 40 cm in the right eye and 0.9 in the left eye, in which he denied any symptoms. Funduscopic examination and OCT findings suggested a RAP-type lesion, so antiangiogenic treatment was started.