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Sturge Weber Syndrome or encephalo-trigeminal angiomatosis is non-hereditary, congenital and rare disorder of unknown aetiology. It is characterised by vascular malformation with capillary venous angiomas involving face, eye and leptomeninges resulting in neurological and orbital manifestations. A case of 23 years old female presented with history of tonic-clonic convulsions, evidence of Port wine stain on face since birth, characteristic CT findings diagnosed as a case of Sturge Weber Syndrome is reported here for its rarity.
View Article and Find Full Text PDFAnesthesia for encephalo-trigeminal angiomatosis (Sturge-Weber syndrome).
Middle East J Anaesthesiol
February 2006
Department of Anesthesia, King Khalid University Hospital, Riyadh, Saudi Arabia.
A case report of rare congenital disease of encephalo-trigeminal angiomatosis (Sturge-Weber Syndrome) (SWS), is presented to alert the anesthesiologist of its potential risk. The case was anesthetized for emergency orthopedic surgery. Anesthesia management is directed towards observing the clinical manifestations of localized superficial skin lesions, extensive systemic involvement, evaluating its associated anomalies and anticipating difficult intubation due to angiomas of the mouth and upper airway and be a ware of concurrent therapy.
View Article and Find Full Text PDFSturge Weber syndrome.
Indian J Dent Res
August 2005
Department of Oral Pathology and Microbiology, College of Dental Surgery, Kasturba Medical College, Mangalore.
A variant of hemangioma and an uncommon congenital condition, the Sturge Weber syndrome (SWS), also called encephalo trigeminal angiomatosis, is a neurocutaneous disorder with angiomas involving the skin of the face (cutaneous angioma) and pia arachnoid (leptomeningeal angioma). It occurs typically in the ophthalmic and maxillary distributions of the trigeminal nerve (1,2). Here we present a case of a 14 year old girl.
View Article and Find Full Text PDF[Sturge-Weber-Krabbe syndrome (or encephalo-trigeminal angiomatosis)].
Ann Dermatol Venereol
April 2004
Service de Dermatologie, Département Peau et Morphologie, CHU, 37044 Tours Cedex 01.
A study of 9 cases of trigeminal noevus flammeus was performed. Eight had congenital glaucoma and where followed from 1 to 10 years. Only three had intracranial involvement.
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