LYMPHOID BLAST CRISIS OF B-LINEAGE PHENOTYPE WITH MONOSOMY-7 IN A PATIENT WITH JUVENILE CHRONIC MYELOGENOUS LEUKEMIA (JCML)

被引:0
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作者
LAU, RC
SQUIRE, J
BRISSON, L
KAMELREID, S
GRUNBERGER, T
DUBE, I
LETARTE, M
SHANNON, K
FREEDMAN, MH
机构
[1] HOSP SICK CHILDREN, DIV HEMATOL ONCOL, TORONTO M5G 1X8, ON, CANADA
[2] HOSP SICK CHILDREN, DEPT IMMUNOL, TORONTO M5G 1X8, ON, CANADA
[3] UNIV TORONTO, DEPT PAEDIAT, TORONTO M5S 1A1, ON, CANADA
[4] UNIV TORONTO, DEPT PATHOL, TORONTO, ON, CANADA
[5] UNIV TORONTO, DEPT IMMUNOL, TORONTO, ON, CANADA
[6] UNIV LAVAL, DEPT PEDIAT, QUEBEC CITY, PQ, CANADA
[7] UNIV CALIF SAN FRANCISCO, DEPT PEDIAT, SAN FRANCISCO, CA 94143 USA
[8] USN HOSP, DEPT CLIN INVEST, OAKLAND, CA USA
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D O I
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中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We studied a patient with juvenile chronic myelogenous leukemia (JCML) whose terminal course was characterized by transformation to acute lymphoblastic leukemia. Karyotypic studies identified monosomy 7 in leukemic myelomonocytic marrow cells during the chronic phase and in the lymphoblasts during the transformation phase. Our ability to sustain the transformed lymphoblasts in culture allowed us to characterize them further. CD19, HLA-DR, and CD10 were present, consistent with a pre-B acute lymphoblastic leukemia phenotype. CD14 (My-4) and CD13 (My-7) were negative. Rearrangement of immunoglobulin heavy- and light-chain genes identified monoclonal populations of cells of the B lineage. This case provides further evidence that JCML is a clonal disease of pluripotent stem-cell origin.
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页码:903 / 908
页数:6
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