1. Long-Smoldering T-prolymphocytic Leukemia: A Case Report and a Review of the Literature.
- Author
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Gjelberg, Hilde K., Helgeland, Lars, Liseth, Knut, Micci, Francesca, Sandnes, Miriam, Russnes, Hege G., and Reikvam, Håkon
- Subjects
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LITERATURE reviews , *LEUKEMIA , *BONE marrow , *OVERALL survival , *LEUCOCYTOSIS - Abstract
T-prolymphocytic leukemia (T-PLL) is a rare malignancy of mature T-cells with distinct clinical, cytomorphological, and molecular genetic features. The disease typically presents at an advanced stage, with marked leukocytosis, B symptoms, hepatosplenomegaly, and bone marrow failure. It usually follows an aggressive course from presentation, and the prognosis is often considered dismal; the median overall survival is less than one year with conventional chemotherapy. This case report describes a patient with T-PLL who, after an unusually protracted inactive phase, ultimately progressed to a highly invasive, organ-involving disease. After initial treatments failed, a novel treatment approach resulted in a significant response. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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