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Published on: March 10, 2026
Lymphomatosis cerebri as a cause of white matter dementia
Karen E Rollins1, B K Kleinschmidt-DeMasters, John R Corboy
1Department of Neurology, University of Colorado School of Medicine, Denver, CO 80262, USA.
Insights
Lymphomatosis cerebri, a rare diffuse form of primary central nervous system lymphoma, can cause rapidly progressive dementia in immunocompetent individuals. This white matter disease infiltrates the entire brain and spinal cord, mimicking other neurological conditions.
Area of Science:
- Neurology
- Oncology
- Pathology
Background:
- Primary central nervous system lymphoma typically presents as a solitary lesion in immunocompetent patients.
- Lymphomatosis cerebri is a rare variant characterized by diffuse infiltration of the brain without a cohesive mass.
- This pattern can mimic other white matter disorders, complicating diagnosis.
Observation:
- Three immunocompetent individuals presented with rapidly progressive dementia.
- Magnetic resonance imaging findings were initially misdiagnosed as Binswanger's disease, leukoencephalopathy, viral infection, or glioma.
- Neuropathologic examination revealed diffusely infiltrating large-cell B-cell lymphoma throughout the white matter, sparing gray matter.
Findings:
- The lymphoma cells permeated the entire brain and spinal cord, with varying cell density.
- Microglial and astrocytic reactions were present, with subtle myelin pallor.
- CD20 immunostaining was crucial for identifying the extent of tumor cell infiltration.
Implications:
- Lymphomatosis cerebri is a neoplastic cause of white matter dementia.
- It expands the differential diagnosis for rapidly progressive dementia syndromes.
- Accurate diagnosis requires considering this rare presentation of CNS lymphoma.
Abstract:
Primary central nervous system lymphoma most often presents as a solitary, isolated lesion in immunocompetent patients. Rarely, the disease presents as a diffuse, infiltrating condition without formation of a cohesive mass, a pattern called lymphomatosis cerebri. We present 3 immunocompetent individuals who developed rapidly progressive dementia. Magnetic resonance imaging features mimicked other disorders of white matter and prompted preoperative diagnoses of Binswanger's disease (subcortical ischemic vascular dementia), unknown leukoencephalopathy, viral infection, or infiltrating glioma. Neuropathologic examination at biopsy (Poon T, Matoso I, Tchertkoff V, Weitzner I Jr, Gade M. CT features of primary cerebral lymphoma in AIDS and non-AIDS patients. J Comput Assist Tomogr . 1989;13:6-9) and autopsy (Schwaighofer BW, Hesselink JR, Press GA, Wolf RL, Healy ME, Berthoty DP. Primary intracranial CNS lymphoma: MR manifestations. Am J Neuroradiol . 1993;10:725-9) demonstrated nonnecrotic, diffusely infiltrating, large-cell B-cell lymphoma of white matter, with relative sparing of gray matter, and without significant leptomeningeal involvement or bulky periventricular disease at autopsy. Microglial and astrocytic reactions, but only subtle myelin pallor, were evident as individual tumor cells permeated the entire brain and spinal cord, albeit with considerable variation in cell density. Individual tumor cells could be identified from the optic nerve to spinal cord, documenting the "whole-brain" nature of the disease. CD20 immunostaining was necessary to fully appreciate the extent of individual lymphoma cell percolation through the white matter. The neurobehavioral deficits manifested by these patients demonstrate that lymphomatosis cerebri is an additional neoplastic cause of white matter dementia and can be added to the growing list of disorders responsible for this syndrome.
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