Melanotic schwannoma of the choroid. Immunohistochemistry and electron microscopic observations.

Abstract

The purpose of this article is to describe what is probably the first reported case of a melanotic schwannoma of the choroid and to discuss the clinical and histopathologic features that serve to differentiate this rare intraocular tumor from a malignant melanoma of the choroid. A 21-year-old woman underwent enucleation of the right eye for a slowly enlarging pigmented choroidal mass that was associated with ipsilateral blindness. The tumor was studied by light microscopy, immunohistochemistry, and electron microscopy. The tumor was composed of fascicles and whorls of pigmented and nonpigmented plump spindle cells that had light microscopic features of a schwannoma. The tumor cells showed immunoreactivity to S-100 protein and HMB-45. Electron microscopy showed cytoplasmic processes surrounded by a continuous basement membrane and abundant extracellular collagen. The pigmented spindle-shaped cells contained melanosomes in different stages of melanogenesis. The findings were compatible with a melanotic schwannoma. Melanotic schwannoma has been reported in soft tissues, peripheral nerves, and in the orbit. To the authors' knowledge, this is the first report of a melanotic schwannoma of the choroid. This extremely rare pigmented choroidal tumor may be very difficult to differentiate clinically from choroidal melanoma.