Sturge-Weber syndrome with pyogenic granuloma

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منابع مشابه

Angiodysplastic Sturge Weber syndrome.

Accepted 19 November 2017 DesCripTion A 3-year-old boy presented with global developmental delay, abnormal craniofacial growth and left focal seizures since infancy. He was the first child of a non-consanguineous couple with unremarkable perinatal period. Family history was non-contributory. On examination, he had macrocephaly (head circumference 55 cm, >3 z-score), extensive port-wine stain di...

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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...

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Sturge-Weber Syndrome

Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome, characterized by the association of facial port-wine hemangiomas in the trigeminal nerve distribution area, with vascular malformation(s) of the brain (leptomeningeal angioma) with or without glaucoma. Herein, we reported Sturge-Weber syndrome in a 50-year-old man, who presented port-wine hemangiomas and epilepsy. In this case, the patie...

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The Sturge-Weber Syndrome

The association of vascular nxvi of the face, predominantly unilateral in distribution, with homolateral changes in the cerebral cortex, has long been of interest to clinicians. The first case4 of this disorder was presented by W. Allen Sturge to the Clinical Society of London in 1879. Weber5 called attention to the characteristic roentgenological features of this disease in 1922, and in 1934. ...

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Sturge-Weber syndrome with bilateral intracranial calcification.

Four children affected by Sturge-Weber syndrome and demonstrating bilateral intracranial calcification are described, bringing up to 21 the number of similar reported cases. The frequency of bilateral hemisphere involvement in this syndrome is not known, but it might be as high as 15%. If present, neurosurgical intervention is, in our opinion, contraindicated.

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ژورنال

عنوان ژورنال: Contemporary Clinical Dentistry

سال: 2013

ISSN: 0976-237X

DOI: 10.4103/0976-237x.118345