Retinoblastoma (RB) is the most frequent malignant intraocular tumor i
n childhood. Six hundred and thirty-six cases with 831 RB-affected eye
s were diagnosed and treated in our specialist center between 1963-199
4. The diagnosis was made by histopathologic examination in 617 cases
and clinically in 19 cases. Four hundred and forty-one (69.3%) cases w
ere unilateral and 195 (30.7%) were bilateral. Two hundred and sixty-e
ight (42.1%) were females and 368 (57.9%) were males. The youngest pat
ient was 20 days old and the oldest was 16 years old at the time of di
agnosis (mean: 2.2 years). In thirty-four (5.3%) cases, a family histo
ry of RB was present. Ten of these cases were unilateral and 24 were b
ilateral. The most frequent presenting signs were leukocoria (394 case
s, 61.9%), buphthalmos (92 cases, 14.5%), and strabismus (68 cases, 10
.7%). The referring initial diagnoses were correct in 519 (81.6%) case
s and false-negative in 117 (18.4%) cases. The most frequent initial f
alse-negative diagnoses of the referring physicians were buphthalmos (
43 cases, 6.8%), endophthalmitis (37 cases, 5.8%), and retinal detachm
ent (12 cases, 1.9%). Apart from these 636 cases, there were 29 false-
positive RB diagnoses during the same study period for which enucleati
on was performed. False-positive diagnoses included endophthalmitis (9
cases), retinal dysplasia (6 cases), retinal detachment (5 cases),vit
reous hemorrhage (4 cases), Coats' disease (4 cases), and toxocariasis
(one case). Ancillary testing for metastasis was carried out in all c
ases with newly diagnosed retinoblastoma. Five hundred and ninety-eigh
t (72%) eyes had intraocular disease and 233 (28%) had extraocular spr
ead. Of these 233 RBs, 58 had systemic disease. Fifty-two out of 58 tu
mors showing systemic involvement had either optic nerve or extrascler
al extension at the histopathologic examination of enucleation materia
l. The remaining six eyes had intraocular Class IV-V RB.