Translocation 11;14 in three children with acute lymphoblastic leukemia of T-cell origin

被引:9
|
作者
Zalcberg, IQ
Silva, MLM
Abdelhay, E
Tabak, DG
Ornellas, MH
Simoes, FV
Pucheri, W
Ribeiro, R
Seuanez, HN
机构
[1] CTR NACL TRANSPLANTE MEDULA OSSEA,RIO JANEIRO,BRAZIL
[2] INST CARLOS CHAGAS FILHO,RIO JANEIRO,BRAZIL
[3] UNIV FED RIO DE JANEIRO,RIO PIEDRAS,PR
[4] UNIV TENNESSEE,ST JUDE CHILDRENS HOSP,COLL MED,DEPT HEMATOL ONCOL,MEMPHIS,TN
[5] UNIV TENNESSEE,ST JUDE CHILDRENS HOSP,COLL MED,DEPT PEDIAT,MEMPHIS,TN
[6] UNIV FED RIO DE JANEIRO,DEPT GENET,BR-21945 RIO JANEIRO,BRAZIL
关键词
D O I
10.1016/0165-4608(95)00062-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Clinical, karyotypic, immunophenotypic, and molecular profiles of three TALL cases carrying a t(11;14) are discussed and compared with data in the literature. As previously reported, t(11;14)(p13;q11) was associated in one patient with a TALL profile of intermediate stage of maturation (CD7 +, CD4 +, CD8 +). However, the same translocation was found to be present in another patient with a more immature, pro-TALL profile (CD7 +, CD4 -, CD8 -). Both patients showed molecular rearrangements of the TCR beta chain gene. A third patient, with a very immature pro-TALL profile (CD34+, CD7 +, CD4-, CD8-), carrying a t(11;14) (p15;q11), showed molecular rearrangements of the TCR beta and gamma chain genes, while the IgH chain genes were in germline configuration. Our data indicate that t(11;14) can also be present in TALLs of more immature stages of intrathymic development; the significant factor determining the clinical behavior of TALLs is apparently related more to cell differentiation than to the presence of this chromosome rearrangement.
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收藏
页码:32 / 38
页数:7
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