Choroidal ganglioneuroma in neurofibromatosis

Springer Science and Business Media LLC - Tập 220 - Trang 25-31 - 1983
J. J. Woog1, D. M. Albert1,2, J. Craft2, N. Silberman3, D. Horns4
1Harvard Medical School, Massachusetts Eye and Ear Infirmary, Massachusetts
2Massachusetts Eye and Ear Infirmary, Boston, USA
3Mercy Hospital, Des Moines, USA
4Minneapolis, USA

Tóm tắt

A twenty-one year old female with previously unsuspected neurofibromatosis presented for evaluation of a blind painful eye. Histopathologic examination of the enucleated specimen revealed choroidal thickening with ovoid bodies and proliferation of connective tissue with pigment-containing cells and ganglion-like cells. Electron microscopic study of the latter cell population revealed typical morphologic features of ganglion cells, including numerous electron-dense intracellular granules and an abundance of mitochondria and rough endoplasmic reticulum. These pathologic findings were interpreted as consistent with the diagnosis of choroidal ganglioneuroma occurring in the context of ocular neurofibromatosis. The literature concerning this unusual tumor is reviewed and the possible relationship of this lesion to neurofibromatosis and other disorders of neural cresent proliferation are briefly discussed.

Tài liệu tham khảo

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