How We Evaluate and Treat Leukemic Presentations of Mature T-Cell Lymphomas

T-cell non-Hodgkin lymphomas, which arise from post-thymic mature T cells, constitute approximately 10-15% of all non-Hodgkin lymphomas. Their leukemic presentations, referred to here as mature T-cell leukemias, are relatively uncommon and present significant diagnostic and therapeutic challenges requiring an informed approach to diagnosis and management. The initial presentation is often persistent T-cell lymphocytosis that must be distinguished from reactive (non-malignant) causes. Unlike B-cell lymphocytosis, where clonality usually indicates malignancy, T-cell clonality can be detected in benign conditions such as autoimmune disorders and viral infections. Thus, establishing clonality is helpful but not sufficient, and a systematic diagnostic approach integrating clinical features, morphology, immunophenotype, and molecular findings is critical. This review outlines our approach to the diagnosis and treatment of four major subtypes of mature T-cell leukemias: T-cell prolymphocytic leukemia (T-PLL), adult T-cell leukemia/lymphoma (ATLL), T-large granular lymphocytic leukemia (T-LGL), and Sézary syndrome (SS). Each section includes a discussion of clinical features, workup, and treatment options.

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Publication Details

Journal
Cancers
Published
2026-03-17
DOI
https://doi.org/10.3390/cancers18060965
Primary Topic
T-cell and Retrovirus Studies
Type
article
Field-Weighted Citation Impact
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article

How We Evaluate and Treat Leukemic Presentations of Mature T-Cell Lymphomas

Arjun Ravishankar, Vinisha Somaya, Francesca Montanari, Haris Qureshi et al.
Cancers
T-cell and Retrovirus Studies
article

How We Evaluate and Treat Leukemic Presentations of Mature T-Cell Lymphomas

Arjun Ravishankar, Vinisha Somaya, Francesca Montanari, Haris Qureshi, M. A. Girardi, Tarsheen Sethi, Ahmad Kiwan, Francine Foss
article en

Abstract

T-cell non-Hodgkin lymphomas, which arise from post-thymic mature T cells, constitute approximately 10-15% of all non-Hodgkin lymphomas. Their leukemic presentations, referred to here as mature T-cell leukemias, are relatively uncommon and present significant diagnostic and therapeutic challenges requiring an informed approach to diagnosis and management. The initial presentation is often persistent T-cell lymphocytosis that must be distinguished from reactive (non-malignant) causes. Unlike B-cell lymphocytosis, where clonality usually indicates malignancy, T-cell clonality can be detected in benign conditions such as autoimmune disorders and viral infections. Thus, establishing clonality is helpful but not sufficient, and a systematic diagnostic approach integrating clinical features, morphology, immunophenotype, and molecular findings is critical. This review outlines our approach to the diagnosis and treatment of four major subtypes of mature T-cell leukemias: T-cell prolymphocytic leukemia (T-PLL), adult T-cell leukemia/lymphoma (ATLL), T-large granular lymphocytic leukemia (T-LGL), and Sézary syndrome (SS). Each section includes a discussion of clinical features, workup, and treatment options.

CancersVol. 18(6)
University of Michigan (US), Yale University (US)
Good health and well-being
Openalex Percentile: Top 19%
T-cell and Retrovirus Studies
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