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Chromosome abnormalities in hairy cell leukaemia variant
Author(s) -
BritoBabapulle Vasantha,
Matutes Estela,
Oscier David,
Mould Sarah,
Catovsky Daniel
Publication year - 1994
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/gcc.2870100308
Subject(s) - genetics , chromosome , biology , gene
We describe chromosome abnormalities in 6 patients with hairy cell leukaemia (HCL) variant, a rare B‐cell disorder with clinical and laboratory features intermediate between HCL and B‐prolymphocytic leukaemia (B‐PLL). All but one had marked splenomegaly and a raised white blood cell count (median 40 × 10 9 /l) with over 80% nucleolated hairy cells. These cells had a B‐cell immunophenotype distinct from that of typical HCL. All patients but one are alive with stable disease with a median follow‐up of 60 months. Numerical chromosome changes included loss of chromosomes 2, 3, 4, 6, 10, 19, 21, and X. Three cases had translocations involving the immunoglobulin gene regions: t(14;17)(q32;q11), t(14;22)(q32;q11), and t(2;8)(p11.12;q24). Immunocytochemistry demonstrated the presence of the MYC protein in cells from the case with t(2;8) but not in two others. Other structural abnormalities included t(3;10)(q27;q22) and t(3;12)(q27;q13) in the same patient, der(17)t(7;10;17) (p11;q27;q22), t(1;3)(q25;p21), t(8;21)(p12;q11), t(17;21)(p11;p11), del(6)(q15), del(7)(q34), and del(14)(q24). Genes Chromosom Cancer 10:197–202 (1994). © 1994 Wiley‐Liss, Inc.