Department of Clinical Laboratory, The First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, 310003, China,
Int J Hematol. 2014 Jan;99(1):87-90. doi: 10.1007/s12185-013-1480-z. Epub 2013 Nov 30.
The JAK2 V617F mutation is common in patients with Philadelphia-negative chronic myeloproliferative neoplasms, but few cases of the JAK2 V617F mutation have been described in Philadelphia-positive chronic myeloid leukemia (CML) patients. Here, we report a 21-year-old female who presented with phenotype of CML in whom BCR-ABL transcript and JAK2V617F mutation co-occurred. These findings were determined through cytogenetic analysis, fluorescence in situ hybridization, and allele-specific (AS) PCR. The patient's BCR-ABL transcript disappeared after 6 months of treatment with imatinib, while the JAK2V617F mutation remained positive. We discuss this case with reference to the current literature.
JAK2 V617F 突变常见于费城染色体阴性慢性骨髓增殖性肿瘤患者,但在费城染色体阳性慢性髓性白血病(CML)患者中很少描述 JAK2 V617F 突变。在这里,我们报告了一名 21 岁女性,其表现为 CML 表型,BCR-ABL 转录本和 JAK2V617F 突变同时存在。这些发现通过细胞遗传学分析、荧光原位杂交和等位基因特异性(AS)PCR 确定。该患者在接受伊马替尼治疗 6 个月后 BCR-ABL 转录本消失,而 JAK2V617F 突变仍为阳性。我们参考当前文献讨论了该病例。