AUTOFLUORESCENCE OF CHOROIDAL NEVUS IN 64 CASES

Abstract

In Brief Purpose: To describe the autofluorescence features of choroidal nevi. Design: Noncomparative case series. Participants: Sixty-four consecutive patients. Methods: Correlation of fundus photography with autofluorescence photography. Main Outcome Measure: Autofluorescence features of choroidal nevus and overlying retinal pigment epithelium (RPE). Results: The mean patient age was 62 years. The choroidal nevus was a mean of 5 mm from the optic disk and foveola. The mean tumor basal dimension was 5.0 mm and mean tumor thickness was 1.0 mm. The choroidal nevus showed hypoautofluorescence in 56%, isoautofluorescence in 19%, and hyperautofluorescence in 25%. The autofluorescence features appeared unaffected by tumor thickness, but increasing tumor base and disrupted overlying RPE appeared to produce slightly brighter autofluorescence. Nevi located in the macular region showed darker hypoautofluorescence than those outside the macular region. Overlying RPE hyperplasia, atrophy, and fibrous metaplasia were generally hypoautofluorescent. Drusen, subretinal fluid, and orange pigment were generally hyperautofluorescent. The brightest hyperautofluorescence was found with orange pigment. Conclusions: Choroidal nevus shows little intrinsic autofluorescence. Overlying RPE alterations show dramatic autofluorescence ranging from dark hypoautofluorescence of RPE atrophy to bright hyperautofluorescence of orange pigment. The autofluorescence features of 64 consecutive patients with choroidal nevus revealed hypoautofluorescence (56%), isoautofluorescence (19%), and hyperautofluorescence (25%). Overlying retinal pigment epithelial hyperplasia, metaplasia, or atrophy showed dark hypoautofluorescence. Overlying drusen, subretinal fluid, and orange pigment showed increasingly bright hyperautofluorescence.