J Korean Acad Rehabil Med.  2002 Dec;26(6):811-814.

Atypical Sturge-Weber Syndrome: A case report

Affiliations
  • 1Department of Physical Medicine and Rehabilitation, Sanggye Paik Hospital, Inje University, Korea. oboist@orgio.net

Abstract

Sturge-Weber syndrome is a congenital neurocutaneous disorder of the vessels of the face, the leptomeninges and the brain. Clinically SWS consists of symptoms and signs including a facial nevus (port-wine stain), seizure, hemiparesis, mental retardation. But only a few reports related to atypical Sturge-Weber syndrome without facial nevus have been published. We report a patient with atypical Sturge-Weber syndrome without any clinical feature except hemiparesis. In neuroimaging studies using brain CT scan and MRI, leptomeningeal angiomatosis was demonstated that is the characteristic feature of Sturge- Weber syndrome. In atypical Sturge-Weber syndrome, there may be late- developed complications such as hemiparesis. In conclusion, neuroimaging study is recommended to confirm diagnosis in suspicious atypical SWS patient.

Keyword

Atypical Sturge-Weber syndrome; Leptomeningeal angiomatosis; Hemiparesis; Late-developed complications

MeSH Terms

Angiomatosis
Brain
Brain Stem Infarctions
Diagnosis
Humans
Intellectual Disability
Magnetic Resonance Imaging
Neurocutaneous Syndromes
Neuroimaging
Nevus
Paresis
Seizures
Sturge-Weber Syndrome*
Tomography, X-Ray Computed
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