Progressive Multifocal Leukoencephalopathy is a demyelinating disease.
MRI shows high signal intensity areas on T2w sequence and low intensi
ty aeras on T1w sequence, without enhancement after intravenous contra
st injection. The involvement of arcuate fiber (U fibers) creates a sh
arp border with the cortex. There is no mass effect. Involvement of pa
rieto-occipital areas is frequent. The lesions may be uni or bilateral
, single or multiple; bilateral lesions are asymmetric. This typical a
ppearance on MR images occurs in 90 % of the patients with PML. Some a
typical patterns may occur: focal hemorrhage, atrophy, faint periphera
l enhancement and involvement of deep gray matter (basal ganglia). In
most cases, the clinical and MR features provide the diagnosis. The ma
in differential diagnosis, in MRI, is HIV-leukoencephalitis, but lesio
ns are diffuse, less intense on T2w sequence and not visible on T1, wi
thout involvement of the arcuate fibers. Stereotactic biopsy should be
performed only for atypical lesions, particularly in case of predomin
ant involvement of deep gray structures.