Infections arising from free-living amebae are rare. They generally ca
use recognizable disease only in chronically ill, debilitated patients
who are immune suppressed. Only about 70 cases of granulomatous amebi
c encephalitis have been reported. We present an unusual case of granu
lomatous encephalitis in a 35-year-old man. Neurologic examination and
laboratory tests were inconclusive. CT demonstrated bilateral low-den
sity areas with mild mass effect in the cortex and subcortical white m
atter, which showed increased signal on T2-weighted MRI. Craniotomy an
d brain biopsy revealed granulomatous encephalitis with acanthamoeba o
rganisms. Though nonspecific, imaging can support the diagnosis of ame
bic encephalitis and direct biopsy.