t(10;16)(q22;p13) and MORF-CREBBP fusion is a recurrent event in acute myeloid leukemia

被引:27
作者
Vizmanos, JL
Larráyoz, MJ
Lahortiga, I
Floristán, F
Alvarez, C
Odero, MD
Novo, FJ
Calasanz, MJ
机构
[1] Univ Navarra, Dept Genet, Sch Sci, E-31080 Pamplona, Spain
[2] Hosp Cruces, Hematol Serv, Serv Vasco Salud Osakidetza, Barcelona, Spain
关键词
D O I
10.1002/gcc.10174
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recently, it was shown that t(10;16)(q22;p13) fuses the MORF and CREBBP genes in a case of childhood acute myeloid leukemia (AML) M5a, with a complex karyotype containing other rearrangements. Here, we report a new case with the MORF-CREBBP fusion in an 84-year-old patient diagnosed with AML M5b, in which the t(I 0; 1 6)(q22;p 13) was the only cytogenetic aberration. This supports that this is a recurrent pathogenic translocation in AML. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:402 / 405
页数:4
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