TRANSLOCATION (2 9)(P12 P23) IN A CASE OF ACUTE-LEUKEMIA WITH T(4 11)(Q21 Q23) - LACK OF REARRANGEMENT OF THE KAPPA AND INTERFERON GENE LOCI

被引:5
|
作者
PAIETTA, E
VANNESS, B
LEBEAU, MM
BENNETT, J
CASSILETH, P
WIERNIK, PH
机构
[1] ALBERT EINSTEIN CANC CTR,BRONX,NY
[2] UNIV MINNESOTA,INST HUMAN GENET,MINNEAPOLIS,MN 55455
[3] UNIV CHICAGO,HEMATOL ONCOL SECT,CHICAGO,IL 60637
[4] UNIV ROCHESTER,MED CTR,DIV MED ONCOL,ROCHESTER,NY 14642
[5] UNIV PENN,CTR CANC,PHILADELPHIA,PA 19104
[6] EASTERN COOPERAT ONCOL GRP,MADISON,WI
关键词
D O I
10.1016/0165-4608(92)90238-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A case is reported of an adult male patient with acute leukemia characterized by the presence of the novel cytogenetic abnormality, t[2;9][p12;p23], in addition to a t[4;11][q21;q23]. The immunophenotype of the blast cell population was consistent with immature early pre-B cell acute lymphoblastic leukemia [ALL] [TdT+,HLA-DR+,CD19+,CD24+/-,CD10-] expressing myelo-monocytic antigens [CDw65,CD15]. The genotype showed a clonal rearrangement of the immunoglobulin heavy chain locus. Because the immunoglobulin kappa [kappa] light chain gene is located on chromosome 2 at band p12 and interferon alpha [alpha] and beta [beta] map to chromosome 9p21-p22, rearrangements of these loci as a result of the t[2;9] were studied. There was no evidence for rearrangement of the region covering about 40 kilobases around the kappa-locus when hybridized to C[kappa], the 3' kappa-enhancer or the kappa deleting element. Only germline size restriction fragments were also found for the interferon alpha and beta genes. The patient's clinical features were typical for ALL associated with the t[4;11], including a high white blood cell count at presentation, hepatosplenomegaly, and a poor outcome. The potential significance of 2p and 9p abnormalities in addition to t[4;11] is discussed.
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页码:82 / 85
页数:4
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