Devi Sandhya G, Goyal Manu, Ramakrishna N V S S, Murthy S Sudha
Department of Laboratory Medicine, Indo-American Cancer Institute and Research Centre, Hyderabad 500 034, India.
Indian J Pathol Microbiol. 2011 Jan-Mar;54(1):176-9. doi: 10.4103/0377-4929.77396.
Rearrangements of the mixed lineage leukemia (MLL) gene at 11q23 commonly occur in infants with CALLA negative B lymphoblastic leukemia (B-ALL). Most often, these are detected by conventional karyotyping; however, fluorescent in-situ hybridization (FISH) with the help of a dual-color break-apart probe is used to identify cryptic translocations. When there is an MLL gene translocation, the usual FISH signal pattern is 1 red-1 green-1 yellow fusion signal pattern. We present a case of an infant with CALLA negative precursor B-ALL with a characteristic translocation t(4;11) (q21;q23), however, with an unusual MLL FISH signal pattern.
11q23处混合谱系白血病(MLL)基因重排常见于普通急性淋巴细胞白血病(CALLA)阴性的婴儿B淋巴细胞白血病(B-ALL)。这些重排大多通过传统核型分析检测;然而,借助双色断裂分离探针的荧光原位杂交(FISH)用于识别隐匿性易位。当存在MLL基因易位时,常见的FISH信号模式是1个红色-1个绿色-1个黄色融合信号模式。我们报告1例CALLA阴性前体B-ALL婴儿病例,其具有特征性易位t(4;11)(q21;q23),但MLL FISH信号模式异常。