Many of the white dot syndromes are considered to have a granulomatous
pathogenesis. The histopathologic characteristics of this case of mul
tifocal choroiditis seen within 15 months of apparent clinical onset s
how that the white dot lesions were nongranulomatous perivascular chor
oidal infiltrates, consisting mainly of B lymphocytes. Early choroidal
neovascularization was also seen.