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Multiple myeloma invasion of the central nervous system
Keith O Schluterman1, Athanasios B-T Fassas, Rudy L Van Hemert
1Department of Neurology, University of Arkansas for Medical Sciences, 4301 W. Markham Street, Little Rock, AR 72205, USA. schlutermankeitho@uams.edu
Background:
Although neurologic manifestations often complicate the course of patients with multiple myeloma (MM), direct central nervous system invasion is rare.
Objective:
To describe the neurologic symptoms and signs, imaging, cerebrospinal fluid findings, and the clinical course of patients with central nervous system myeloma invasion, all of whom had leptomeningeal myelomatosis.
Design And Participants:
Review of 23 patients with MM and leptomeningeal myelomatosis proven by malignant plasma cells in their cerebrospinal fluid.
Setting:
Tertiary-care university medical center.
Results:
Twenty-one patients had advanced-stage MM. Leptomeningeal myelomatosis was diagnosed up to 29 months (median, 13 months) after diagnosis of MM. Symptoms precipitating neurologic evaluation included manifestations of diffuse cerebral dysfunction, cranial nerve palsies, and spinal radiculopathies. Cerebrospinal fluid was abnormal in all patients, usually exhibiting pleocytosis and elevated protein content, plus positive cytologic findings. Specific magnetic resonance imaging findings suggestive of central nervous system invasion were found in 70% of the patients. These included leptomeningeal contrast enhancement and evidence of meningeal-based lesions sometimes masquerading as intraparenchymal lesions. Despite aggressive systemic and local treatment, the outcome was poor, reflecting the aggressiveness of the underlying MM.
Conclusion:
Leptomeningeal myelomatosis, although rare, should be considered in patients with MM and symptoms suggestive of widespread nervous system involvement.
Insights
Direct central nervous system invasion by multiple myeloma (MM) is rare but can cause significant neurologic symptoms. Early consideration of leptomeningeal myelomatosis is crucial for patients with MM experiencing widespread nervous system issues.
Area of Science:
- Neurology
- Oncology
- Hematology
Background:
- Neurologic manifestations are common in multiple myeloma (MM).
- Direct central nervous system (CNS) invasion by MM is infrequent.
- Leptomeningeal myelomatosis represents a rare but serious complication.
Purpose of the Study:
- To characterize neurologic symptoms, signs, and imaging findings in patients with CNS myeloma invasion.
- To analyze cerebrospinal fluid (CSF) findings in leptomeningeal myelomatosis.
- To describe the clinical course and outcomes of patients with leptomeningeal myelomatosis.
Main Methods:
- Retrospective review of 23 patients with multiple myeloma and confirmed leptomeningeal myelomatosis.
- Analysis of clinical data, neurologic examinations, CSF analysis, and magnetic resonance imaging (MRI) findings.
- Evaluation of treatment responses and patient outcomes.
Main Results:
- Leptomeningeal myelomatosis occurred in patients with advanced-stage MM, diagnosed a median of 13 months after MM diagnosis.
- Common presenting symptoms included cerebral dysfunction, cranial nerve palsies, and spinal radiculopathies.
- CSF analysis revealed abnormalities in all patients, with MRI showing suggestive findings in 70%.
Conclusions:
- Leptomeningeal myelomatosis is a rare complication of multiple myeloma.
- It presents with diverse neurologic symptoms and characteristic CSF and imaging findings.
- Despite treatment, the prognosis remains poor, underscoring the need for early recognition.
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