Progressive multifocal leukoencephalopathy: cavitary white matter lesions
Document Type
Article
Publication Date
11-1-2012
Publication Title
The Journal of the Louisiana State Medical Society
Abstract
Progressive Multifocal Leukoencephalopathy (PML) is a fatal demyelinating disorder of the central nervous system caused by the opportunistic neurotropic Polyomavirus JCV. PML typically presents in immunocompromised individuals; is considered an AIDS defining condition; and is clinically characterized by cognitive defects, coordination problems, limb paresis, and speech disturbances. MRI can identify the characteristic bilaterally asymmetrical lesions that favor the subcortical frontal and parietal lobes as hypo-intensities on T1-weighted images and as hyper-intensities on T2-weighted images. Grossly, these areas appear discolored by a dusky, yellow-brown hue with the rare appearance of cavitation. No known therapeutic agent can specifically halt the progression of PML, and survival time after diagnosis averages less than two years. In this submission, we present a photo depicting striking lesions of severe PML of the cavitary type.
First Page
332, 334
Last Page
5
PubMed ID
23431676
Volume
164
Issue
6
Recommended Citation
Alquist, Caroline Raasch; McGoey, Robin; and Del Valle, Luis, "Progressive multifocal leukoencephalopathy: cavitary white matter lesions" (2012). School of Medicine Faculty Publications. 2298.
https://digitalscholar.lsuhsc.edu/som_facpubs/2298