Purpose: The authors report the clinical, cytologic, and histopatholog
ic findings of a unilateral retinoblastoma occurring in a 26-year-old
woman, This tumor usually affects young children; the mean age at the
time of diagnosis usually ranges from 10 to 25 months. Methods: Histop
athologic examination of the enucleated right eye included using stand
ard techniques, as well as immunohistochemical stains of formalin-fixe
d, paraffin-embedded tissues. Results: Histologic examination of secti
ons of the eye showed a retinal tumor that was centered in the equator
ial region and had the typical features of a poorly differentiated ret
inoblastoma. Focal choroidal invasion and seeding of the anterior and
posterior chambers were observed. Immunoreactivity of the tumor cells
for neuron-specific enolase confirmed that the tumor is a neuronal neo
plasm consistent with retinoblastoma. Conclusion: Retinoblastoma occur
ring in adults is a rare finding, In most large series of retinoblasto
mas, no adults are included. Only eight patients 20 years of age or ol
der with retinoblastomas have been documented previously. In the curre
nt case, the patient had no evidence of orbital recurrence or metastas
is 6 years after enucleation of the eye, It may be important for clini
cians to consider this diagnosis when confronted with a retinal mass o
f unknown etiology in adults.