Translocation (4;11)(p12;q23) with rearrangement of FRYL and MLL in therapy-related acute myeloid leukemia

被引:3
|
作者
Sait, Sheila N. J.
Claydon, Melinda A.
Conroy, Jeffrey M.
Nowak, Norma J.
Barcos, Maurice
Baer, Maria R.
机构
[1] Roswell Pk Canc Inst, Dept Pathol, Clin Cytogenet Lab, DNA Microarray & Genom Facil, Buffalo, NY 14263 USA
[2] Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
关键词
D O I
10.1016/j.cancergencyto.2007.05.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Reciprocal chromosomal translocations involving the MLL gene at chromosome region 11q23 are recurring cytogenetic abnormalities in both de novo and therapy-related acute myeloid leukemia (AML) and in acute lymphoblastic leukemia. We report a t(4;11)(p12;q23) with rearrangement of MLL and FRYL (also known as AF4p12), a human homolog to the furry gene of Drosophila, in an adult patient with therapy-related AML after fludarabine and rituximab therapy for small lymphocytic lymphoma and radiation therapy for breast carcinoma. To our knowledge, t(4; I 1)(p I 2;q23) has been reported in two previous patients, and MLL and FRYL rearrangement was demonstrated in one of them. Both of the previous patients had therapy-related leukemias after exposure to topoisomerase 11 inhibitors, whereas our patient had received cytotoxic therapy that did not include a topoisomerase 11 inhibitor. Thus, t(4;11)(p12;q23) with MLL and FRYL involvement represents a new recurring I I q23 translocation, to date seen only in therapy-related acute leukemias. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:143 / 146
页数:4
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