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Published on: December 27, 2024
Malignant spinal meningioma in a CD-1 mouse
Emmanuelle Balme1, Daniel Robert Roth, Elias Perentes
1Department of pathology, Veterinary School of Alfort, 94704 Maisons-Alfort, France.
Abstract:
Spontaneous meningiomas are extremely rare tumors in small laboratory animals, except in some strains of rats and in the B6C3F1 mouse. We report the case of a male CD-1 mouse in poor health condition, with severe apathy and partial paresis of hindlegs. No macroscopic lesion was noticed at necropsy. Microscopic examination revealed the presence of a malignant meningioma (approximately 3mm in diameter) at the distal lumbar level of the spinal cord, invading the vertebral canal, and bilaterally the ventral and dorsal nerve roots and the dorsal root ganglia. The tumor displayed highly cellular sheets of polygonal cells with a well-delineated, abundant, eosinophilic cytoplasm and scarce fibrovascular stroma; epithelioid and sarcomatous areas were also present. The mitotic activity was moderate. Tumor cells expressed vimentin immunoreactivity and were negative for periodic acid-Schiff (PAS), silver impregnation for reticulin, chromogranin A, glial fibrillary acidic protein (GFAP), cytokeratin (CK) and S-100 protein. The diagnosis of malignant spinal meningioma was based on the morphologic features of the neoplasm, the evidence of local invasion and the immunohistochemical results.
Insights
Spontaneous malignant spinal meningiomas are rare in mice. This case report details a malignant meningioma in a CD-1 mouse, highlighting its spinal cord invasion and unique immunohistochemical profile.
Area of Science:
- Veterinary Pathology
- Oncology
- Neuroscience
Background:
- Spontaneous meningiomas are uncommon in laboratory animals, with exceptions in specific rat strains and B6C3F1 mice.
- Meningiomas are tumors arising from the meninges, the membranes surrounding the brain and spinal cord.
Observation:
- A male CD-1 mouse presented with severe apathy and hindleg paresis.
- Necropsy revealed no macroscopic lesions, but microscopic examination identified a 3mm malignant meningioma in the distal spinal cord.
Findings:
- The tumor invaded the vertebral canal, nerve roots, and dorsal root ganglia.
- Histopathology showed a highly cellular neoplasm with epithelioid and sarcomatous areas, moderate mitotic activity, and vimentin immunoreactivity.
- Immunohistochemistry was negative for PAS, reticulin, chromogranin A, GFAP, cytokeratin, and S-100 protein.
Implications:
- This case expands the understanding of spontaneous meningioma occurrence in CD-1 mice.
- The findings contribute to the differential diagnosis of spinal cord tumors in laboratory rodents.
- Detailed histopathological and immunohistochemical characterization is crucial for accurate diagnosis of rare neoplasms.
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