CASE REPORT
Year : 2014  |  Volume : 7  |  Issue : 4  |  Page : 497-501

Spectrum of CT and MR findings in Sturge-Weber syndrome: A case report


Department of Radiodiagnosis, Padmashree Dr. D.Y. Patil Medical College, Hospital and Research Centre, Dr. D.Y. Patil Vidyapeeth, Pimpri, Pune, India

Correspondence Address:
Pallavi J Agrawal
Resident IIIrd year, Dr. D.Y. Patil Medical College, Department of Radiodiagnosis, Sant Tukaram Nagar, Pimpri, Maharashtra
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0975-2870.135284

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Sturge-Weber syndrome is an uncommon, sporadically occurring neurocutaneous syndrome characterized by port wine stain (facial nevus flammeus), congenital glaucoma, and anomalous leptomeningeal angiomatous malformation. Port wine stain is usually the first component of the syndrome. Seizures of the side contralateral to the port wine stain occur early in infancy and worsen with age. Radiological investigations, like computed tomography and magnetic resonance imaging are most useful, playing a pivotal role in demonstrating the cerebral changes. We report the case of a 10-month-old infant presenting with port wine stain over face, trunk, and extremities, hemiparesis of the left side of the body, and new onset of seizure. This case highlights the various neurological manifestations of Sturge-Weber syndrome and how imaging helps to characterize each.


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