Article ID Journal Published Year Pages File Type
4013521 Journal of American Association for Pediatric Ophthalmology and Strabismus 2013 5 Pages PDF
Abstract

Sturge-Weber syndrome is a nonhereditary congenital neurocutaneous syndrome characterized by leptomeningeal angiomatosis, facial nevus flammeus, and diffuse choroidal hemangioma, which when complicated by total retinal detachment, portend a poor prognosis. Management is often limited to salvage external beam irradiation. We present a modified proton therapy technique for young children with total bullous retinal detachments that uses standard fractionation low-dose proton radiotherapy to decrease the risk of radiation complications. Treatment techniques for young children who cannot cooperate with conventional radiation protocols are also described.

Related Topics
Health Sciences Medicine and Dentistry Ophthalmology
Authors
, , , ,