Sturge-Weber Syndrome with Port Wine Stain and Bilateral Choroid Plexus Angiomas: A Case Report
نویسندگان
چکیده
منابع مشابه
Pyogenic Granuloma in a Patient of Sturge-Weber Syndrome with Bilateral Port Wine Stain- A Rare Case Report
Ó Abstract Sturge-Weber syndrome (SWS) also known as encephalotrigeminal angiomatosis. It is a neurocutaneous syndrome, characterized by a facial vascular birthmark and neurological abnormalities. An ipsilateral or bilateral facial cutaneous vascular malformation Port Wine Stain (PWS) usually affects the upper face. Other clinical manifestations are seizures, glaucoma, hemiparesis, mental retar...
متن کاملPort Wine Stains and Sturge-weber Syndrome
It is important for general practitioners to recognize cutaneous port-wine stains as these could signify important association with Sturge Weber syndrome, where neurological and ocular complications are likely. As importantly, advances in technology in the past two decades have made laser the standard of care for the management of port-wine stains. Port-wine stains are venous ectasias that are ...
متن کاملChoroid plexus size in young children with Sturge-Weber syndrome.
PURPOSE To assess the size of the choroid plexus in young children with unilateral and bilateral Sturge-Weber syndrome. METHODS Subjects included 15 children 4 years old or younger with Sturge-Weber syndrome. Eleven cases were unilateral and four were bilateral. Unilateral or bilateral involvement was determined by the distribution of abnormal leptomeningeal enhancement on MR images. The diam...
متن کاملHypothyroidism and Sturge-Weber Syndrome associated with Bilateral Port-wine Nevus
Sturge-Weber syndrome (SWS) is a rare, nonhereditary developmental condition that is characterized by a hamartomatous vascular proliferation of the brain, resulting in multiple angiomas that occur on the same side due to arteriovenous malformations. It is believed to be caused by persistence of a vascular plexus around the cephalic portion of the neural tube and is present at birth in about 1 i...
متن کاملBilateral Sturge Weber syndrome- a rare case report.
BACKGROUND Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. OBJECTIVE To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. CASE We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcif...
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ژورنال
عنوان ژورنال: Journal of Medicine
سال: 2014
ISSN: 2075-5384,1997-9797
DOI: 10.3329/jom.v15i1.19877