Abstract
Objective: To compare the clinical features of primary vs secondary retinal vasoproliferative tumors (VPTs). Methods: Retrospective case series of 334 tumors in 295 eyes of 275 patients. Results: Of 275 patients with VPT, 41% (n=113) were male and 59% (n=162) were female, with a mean age of 44 years at presentation. Primary VPT occurred in 80% (n=219) and secondary VPT, in 20% (n=56) of patients. Secondary VPT (n=67) occurred in eyes with retinitis pigmentosa (n=15, 22%), pars planitis (n=14, 21%), Coats disease (n=11, 16%), previous retinal detachment surgery (n=8, 12%), idiopathic peripheral retinal vasculitis (n=4, 6%), familial exudative vitreoretinopathy (n=3, 4%), and others (n=12, 18%). The mean interval between diagnosis of underlying ocular condition and secondary VPT was 160 months. Statistically significant differences (P
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CITATION STYLE
Shields, C. L., Kaliki, S., Al-Dahmash, S., Rojanaporn, D., Shukla, S. Y., Reilly, B., & Shields, J. A. (2013). Retinal vasoproliferative tumors: Comparative clinical features of primary vs secondary tumors in 334 cases. JAMA Ophthalmology, 131(3), 328–334. https://doi.org/10.1001/2013.jamaophthalmol.524
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