“…71,72 Today, MRI appears to be replacing CT as the preferred method of detecting and delineating intracranial abnormalities in patients with suspected Sturge-Weber syndrome. 27,75,76 Neuropathologic manifestations of Sturge-Weber syndrome include leptomeningeal angiomatosis, herniatrophy, cortical calcification, venous engorgement, choroid plexus angiomatosis, and patchy parenchymal gliosis and demyelination.14,27 The leptomeningeal angioma is the primary lesion responsible for neurologic symp¬ toms.76 This venous malformation consists of thin-walled vessels that lie in the pia of the posterior parietal, tem¬ poral, and anterior occipital lobes.77 Atrophy and calci¬ fication occur in the underlying cerebral cortex in a pericapillary distribution in about two thirds of cases.71 The "railroad track" calcification pattern follows the brain convolutions and tends to increase in density until the end ofthe second decade.72 The calcification is thought to be due to anoxic injury caused by stasis of blood in the angiomatous leptomeningeal vessels or by some abnor¬ mality of the permeability of these vessels.14 Bihemispheric involvement, estimated to occur in 15% of cases,78 is a poor prognostic sign.79…”