RETINOBLASTOMA IN TURKEY - DIAGNOSIS AND CLINICAL CHARACTERISTICS

Citation
I. Gunalp et al., RETINOBLASTOMA IN TURKEY - DIAGNOSIS AND CLINICAL CHARACTERISTICS, Ophthalmic genetics, 17(1), 1996, pp. 21-27
Citations number
16
Categorie Soggetti
Genetics & Heredity",Ophthalmology
Journal title
ISSN journal
13816810
Volume
17
Issue
1
Year of publication
1996
Pages
21 - 27
Database
ISI
SICI code
1381-6810(1996)17:1<21:RIT-DA>2.0.ZU;2-X
Abstract
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.