Central Nervous System T-cell Lymphoma Research Articles

Non‐HTLV‐I associated pleomorphic T‐cell lymphoma of the brain mimicking post‐vaccinal acute inflammatory demyelination

Two weeks after vaccination against tick-borne encephalitis (TBE), a 57-year-old female suddenly developed mental confusion and hemiparesis of the left side. Cranial MRI demonstrated extensive bilateral lesions in the fronto-parietal white matter of both hemispheres, suggesting an acute inflammatory demyelinating disease following vaccination. Despite administration of high-dose corticosteroids, the patient died 3 weeks after onset of neurological symptoms. Autopsy revealed diffuse infiltrates of a primary cerebral pleomorphic T-cell lymphoma of medium and large cell type. PCR on brain tissue for HTLV-I and serology for anti-HTLV-I antibodies in CSF and serum were negative; immunocytochemistry on brain tissue did not detect EBV-related antigen. This is the first recorded observation of a diffusely infiltrating primary central nervous system T-cell lymphoma, clinically and radiologically mimicking a fatal acute inflammatory demyelinating complication after vaccination.

Primary central nervous system T‐cell lymphoma with a predominant CD8 immunophenotype

Primary T-cell lymphomas of the central nervous system are uncommon neoplasms. A case of a primary central nervous system T-cell lymphoma in a 66-year-old female who died 8 months after surgery is described. The biopsy specimen was evaluated by routine histology, immunohistochemistry, flow cytometry, and Southern blotting/DNA hybridization. The neoplasm was composed of pleomorphic medium and large cells. Virtually all of the neoplastic cells reacted with antibodies to CD3, CD5, and CD8. Multiple rearranged bands were detected with the T-cell receptor beta-chain gene probe. To the authors' knowledge, this is the first description of a primary central nervous system T-cell lymphoma composed of a predominant population of CD8-expressing T cells, and the first case confirmed by Southern blotting/DNA hybridization.

Primary central nervous system T-cell lymphoma with a predominant CD8 immunophenotype

Primary central nervous system T-cell lymphoma with a predominant CD8 immunophenotype

Primary central nervous system T-cell lymphoma

Primary central nervous system (CNS) T-cell lymphoma is extremely rare. The present case report provides immunocytochemical evidence for a cerebellar CNS T-cell lymphoma. The patient underwent surgery followed by radiation therapy and is alive and well 36 months postoperatively. The clinical and pathological features of primary CNS T-cell lymphoma as well as diagnostic measures and treatment options are discussed, together with a compilation of all previous case reports of primary CNS T-cell lymphomas.