Related Experiment Video
Updated: May 13, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Progressive multifocal leukoencephalopathy: cavitary white matter lesions
Caroline Raasch Alquist1, Robin McGoey, Luis Del Valle
1Department of Pathology, Louisiana State University Health Sciences Center, New Orleans, USA.
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.
Insights
Progressive Multifocal Leukoencephalopathy (PML), a severe brain condition caused by JCV virus, affects immunocompromised individuals. This photo showcases characteristic cavitary lesions, highlighting the disease's aggressive nature.
Area of Science:
- Neurology
- Virology
- Radiology
Background:
- Progressive Multifocal Leukoencephalopathy (PML) is a fatal demyelinating disease of the central nervous system.
- It is caused by the opportunistic neurotropic Polyomavirus JCV and primarily affects immunocompromised individuals, including those with AIDS.
- Clinical manifestations include cognitive decline, motor deficits, and speech impairment.
Observation:
- This case presents a rare example of severe PML with cavitation.
- Characteristic MRI findings include bilaterally asymmetrical lesions in the subcortical frontal and parietal lobes.
- Lesions appear as T1 hypo-intensities and T2 hyper-intensities, with gross discoloration and potential cavitation.
Findings:
- The presented case illustrates striking cavitary lesions indicative of severe PML.
- The imaging findings align with established radiological markers for PML.
- The gross pathology reveals characteristic dusky, yellow-brown discoloration.
Implications:
- This visual documentation aids in understanding the severe manifestations of PML.
- Recognizing these lesions is crucial for timely diagnosis and management, despite the lack of specific treatments.
- The case underscores the devastating impact of JCV in immunocompromised patients.
Related Concept Videos
Cerebral Edema ll: Pathophysiology
Alzheimer Disease ll: Pathophysiology
Encephalitis ll: Pathophysiology
Encephalitis l: Introduction
Dementia l: Introduction
Brain Abscess l: Introduction

