Abstract
In a 10-year study of T-cell acute lymphoblastic leukemias (T-ALL) in children, we have identified five cases expressing the T-cell receptor τδ(TCRτδ). The incidence (26%) of TCRτδ+ T-cell leukemias in our material was high. Clinically, the TCRτδ+ leukemias represented a distinct subgroup of T-cell leukemias. Mean age at onset of disease, 1.8 years, was remarkably low for mature T-cell leukemias. White blood cell counts were high, lymph node enlargements were discrete, and no mediastinal tumors were seen. Four of five TCRτδ+ leukemias carried rearrangements of the Cτ2 gene, and transcribed the T-early alpha genetic element. © 1991 by The American Society of Hematology.
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CITATION STYLE
Alfsen, G. C., Beiske, K., Holte, H., Hovig, E., Deggerdal, A., Sandlie, I., … Bolhuis, R. L. H. (1991). T-cell receptor τδ+/CD3+4-8- T-cell acute lymphoblastic leukemias: A distinct subgroup of leukemias in children. A report of five cases. Blood, 77(9), 2023–2030. https://doi.org/10.1182/blood.v77.9.2023.2023
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