Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4013521 | Journal of American Association for Pediatric Ophthalmology and Strabismus | 2013 | 5 Pages |
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.
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Authors
Yoshihiro Yonekawa, Shannon M. MacDonald, Yevgeniy Shildkrot, Shizuo Mukai,