ABSTRACT Adult T-cell leukemia/lymphoma (ATLL) is a rare lymphoid neoplasm associated with human T-cell lymphotropic virus type 1 (HTLV-1). The disease has a heterogeneous presentation and central nervous system (CNS) involvement occurs in 5-20% of cases, usually with concomitant systemic disease. We present a case of a 45 years-old female, previously known to be a HTLV-1 carrier, who developed neurologic symptoms and was finally diagnosed with primary CNS ATLL after imaging studies and flow cytometry analysis of cerebrospinal fluid showed a proliferation of clonal T cells.
Almeida et al. (Mon,) studied this question.
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