## Abstract Tβcell prolymphocytic leukemia (TβPLL) is a rare malignant proliferation of lymphoid cells with a postthymic phenotype. Previous cytogenetic and molecular studies reported complex karyotypes with recurrent chromosomal abnormalities, including translocations involving either __TCL1__ at
T-Cell Prolymphocytic Leukemia With Hemorrhagic Gastrointestinal Involvement and a New Chromosomal Abnormality
β Scribed by Shigeo Toyota; Norihiko Nakamura; Kazuo Dan
- Book ID
- 105675333
- Publisher
- Carden Jennings Publishing
- Year
- 2002
- Tongue
- English
- Weight
- 833 KB
- Volume
- 75
- Category
- Article
- ISSN
- 0925-5710
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π SIMILAR VOLUMES
We report a lS-month+ld boy with acute leukemic cells demonstrated a translocation myelornonocytic leukemia [French-Ameri-46,XY, t(9;11)(p24;q12) that has not been d e can-British classification M4 (FAB-M4)] whose scribed previously.
The majority of published cases of prolymphocytic leukemia (PLL) have been of B-cell origin. Nineteen cases of PLL of T-cell type have been described, as has a single case of PLL having a surface phenotype with features of both B-cells and T-cells. This report presents a review of these cases and co