Introduction: Sturge-weber syndrome (SWS) is a rare condition that presents with a typical facial port-wine stain, neurological manifestations such as seizures, and ocular involvement by glaucoma and/or choroidal hemangioma. In this series we demonstrate the histopathological details of the primary ocular involvement as well as the late blinding secondary ocular changes.
Presentation Of Cases: Seven cases were included with the diagnosis of choroidal hemangioma in association with SWS (6 enucleations and one evisceration).