PURPOSE. TO report a case showing adult-onset foveomacular vitelliform dyst
rophy (AOFVD), associated with vascularized pigment epithelial detachment.
CASE REPORT. A 72-year-old female affected by AOFVD complained with blurred
vision and metamorphopsia in her right eye, seven months after a routinary
clinical examination. Visual acuity in right eye dropped from 0.6 to 0.3,
and biomicroscopic fundus examination revealed a serous pigment epithelial
detachment arising from the temporal margin of the pseudovitelliform lesion
. Fluorescein angiography showed an uneven filling of the pigment epithelia
l detachment, suggesting the presence of a subfoveal choroidal neovasculari
sation, which was confirmed by indocyanine green angiography.
DISCUSSION. The association between AOFVD and vascularized pigment epitheli
al detachment, supports the hypothesis that AOFVD may be a different subgro
up of age-related macular degeneration with specific genetic predisposition
.