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Published on: August 4, 2011
A rare case of retinocytoma occurring in a 12-year-old child
Aylin Yaman1, Kaan Gündüz, Osman Saatci
1Department of Ophthalmology, 9 Eylül University Faculty of Medicine, Izmir, Turkey.
Abstract:
A 12-year-old girl with a translucent, partially calcified retinal mass in the posterior pole surrounded by a rim of pigment epithelial changes and chorioretinal atrophy was diagnosed as having retinocytoma. The patient received a single treatment of transpupillary thermotherapy at the slit lamp to prevent malignant transformation. The dimensions of the lesion and the visual acuity remained unchanged at 3.5 years of follow-up with no further treatment. Retinocytoma is a benign retinal tumor that carries the same genetic implications as retinoblastoma. Regular follow-up is necessary because the tumor can demonstrate malignant transformation.
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