T-prolymphocytic leukemia: TCL1 or MTCP1 rearrangement is not mandatory to establish diagnosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Cancer Research,Hematology
Link
https://www.nature.com/articles/s41375-023-01956-3.pdf
Reference10 articles.
1. Staber PB, Herling M, Bellido M, Jacobsen ED, Davids MS, Kadia TM, et al. Consensus criteria for diagnosis, staging, and treatment response assessment of T-cell prolymphocytic leukemia. Blood. 2019;134:1132–43.
2. Stengel A, Kern W, Zenger M, Perglerova K, Schnittger S, Haferlach T, et al. Genetic characterization of T-PLL reveals two major biologic subgroups and JAK3 mutations as prognostic marker. Genes Chromosomes Cancer. 2016;55:82–94.
3. Soma L, Cornfield DB, Prager D, Nowell P, Bagg A. Unusually indolent T-cell prolymphocytic leukemia associated with a complex karyotype: is this T-cell chronic lymphocytic leukemia? Am J Hematol. 2002;71:224–6.
4. Cavazzini F, Cuneo A, Bardi A, Castoldi G. Indolent T-cell prolymphocytic leukemia: a case report and a review of the literature. Am J Hematol. 2003;74:145–7.
5. Kussick SJ, Wood BL, Sabath DE. Mature T cell leukemias which cannot be adequately classified under the new WHO classification of lymphoid neoplasms. Leukemia. 2002;16:2457–8.
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