Boeckx Nancy, van der Velden Vincent H J, Boogaerts Marc, Hagemeijer Anne, Vandenberghe Peter, van Dongen Jacques J M
Department of Laboratory Medicine, Laboratory of Haematology, University Hospital Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium.
Haematologica. 2004 Aug;89(8):ECR28.
We describe a case of a 38-year old male with inv(16)(p13q22) positive acute myeloid leukaemia (AML) with eosinophilia, relapsing after a molecular remission of almost three years. Remarkably, the leukaemia at relapse was identified as a precursor-B-cell acute lymphoblastic leukaemia (B-ALL) by cytology and immunophenotyping, but was inv(16)(p13q22) positive as revealed by interphase FISH, FICTION analysis, and real-time quantitative PCR. Analysis of immunoglobulin and T-cell receptor genes showed a bi-allelic DH2-JH rearrangement at relapse, but not at diagnosis. These findings indicate a myeloid to lymphoid lineage switch from an inv(16)(p13q22) positive leukaemia and show that IGH gene rearrangements can occur in the presence of CBFB-MYH11 fusion transcripts.
我们描述了一例38岁男性,患有inv(16)(p13q22)阳性伴嗜酸性粒细胞增多的急性髓系白血病(AML),在接近三年的分子缓解后复发。值得注意的是,复发时的白血病通过细胞学和免疫表型分析被鉴定为前体B细胞急性淋巴细胞白血病(B-ALL),但间期荧光原位杂交(FISH)、FICTION分析和实时定量PCR显示其为inv(16)(p13q22)阳性。免疫球蛋白和T细胞受体基因分析显示,复发时存在双等位基因DH2-JH重排,而诊断时未出现。这些发现表明,inv(16)(p13q22)阳性白血病发生了从髓系到淋巴系的谱系转换,并表明在存在CBFB-MYH11融合转录本的情况下可发生IGH基因重排。