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Sturge-Weber Syndrome

By

M. Cristina Victorio

, MD, Akron Children's Hospital

Last full review/revision Aug 2021| Content last modified Aug 2021
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Sturge-Weber syndrome is a congenital vascular disorder characterized by a facial port-wine nevus, a leptomeningeal angioma, and neurologic complications (eg, seizures, focal neurologic deficits, intellectual disability). Diagnosis is clinical. Treatment is symptomatic.

Sturge-Weber syndrome is a neurocutaneous syndrome that occurs in 1 in 50,000 people. Sturge-Weber syndrome is not inherited. It is caused by a somatic mutation (a change in DNA that occurs after conception in the precursors of the affected area) in the GNAQ gene on chromosome 9q21.

Sturge-Weber syndrome causes a capillary malformation called a port-wine nevus (or sometimes a stain or birth mark) typically on the forehead and upper eyelid in the distribution of the 1st and/or 2nd division of the trigeminal nerve. A similar vascular lesion—leptomeningeal angioma—occurs in 90% of patients when the port-wine nevus involves upper and lower eyelids on one side but occurs in only 10 to 20% when only one eyelid is affected. Usually, the nevi and leptomeningeal angiomas are unilateral, but, rarely, patients have bilateral port-wine nevi in the distribution of the 1st division of the trigeminal nerve and bilateral leptomeningeal angiomas.

A port-wine nevus may occur without a leptomeningeal angioma and its accompanying neurologic signs; in such cases, the eyes and eyelids may or may not be involved. Rarely, a leptomeningeal angioma occurs without the port-wine nevus and ocular involvement.

Neurologic complications of Sturge-Weber syndrome include seizures, focal neurologic deficits (eg, hemiparesis), and intellectual disability.

Often, the involved cerebral hemisphere progressively atrophies.

Symptoms and Signs of Sturge-Weber Syndrome

The port-wine nevus can vary in size and color, ranging from light pink to deep purple.

Seizures occur in about 75 to 90% of patients and typically start by age 1 year. Seizures are usually focal but can become generalized. Hemiparesis of the side opposite the port-wine nevus occurs in 25 to 50% of patients. Sometimes the hemiparesis worsens, especially in patients whose seizures cannot be controlled.

Diagnosis of Sturge-Weber Syndrome

  • Brain MRI or head CT

Diagnosis of Sturge-Weber syndrome is suggested by a characteristic port-wine nevus.

Brain MRI with contrast is used to check for a leptomeningeal angioma, but the angioma may not yet show up in very young children. If MRI is not available, head CT may be done; it may show calcifications in the cortex under the leptomeningeal angioma. The parallel curvilinear railroad-track calcifications seen on skull x-rays as mentioned in older literature develop during adulthood.

A neurologic examination is done to check for neurologic complications, and an ophthalmologic examination is done to check for eye complications.

Treatment of Sturge-Weber Syndrome

  • Symptomatic treatment

Low-dose aspirin is usually given, starting at the time of diagnosis, to help prevent strokes or lessen the progressive hemispheric atrophy presumably by preventing sludging in the abnormal capillaries.

Selective photothermolysis (pulsed-dye laser) can lighten the port-wine nevus.

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