山东大学学报(医学版) ›› 2017, Vol. 55 ›› Issue (2): 79-83.doi: 10.6040/j.issn.1671-7554.0.2015.533
周兰兰,潘学谊,郭煜
ZHOU Lanlan, PAN Xueyi, GUO Yu
摘要: 目的 分析急性混合细胞表型白血病(MPAL)临床特点、生物学特征、疗效及预后。 方法 根据2008年WHO血液肿瘤分类标准,回顾性分析了48例MPAL患者(MPAL组)的病历资料,以同期50例伴淋系抗原表达的AML(Ly+AML)患者(Ly+AML组)作为对照。采用常规瑞士染色及细胞化学染色进行细胞形态学分析,采用流式细胞术进行细胞免疫分型,采用荧光原位杂交技术检测白血病常见融合基因,采用常规G显带技术分析染色体核型。 结果 MPAL组发病中位年龄显著大于Ly+AML组(54岁 vs 30岁,P<0.05),其CD34阳性率、异常染色体核型发生率及Ph染色体核型发生率也显著高于Ly+AML组(85.4% vs 50.0%,65.3% vs 35.7%,23.0% vs 0%, P均<0.05)。MPAL总体生存时间(OS)及无复发生存时间(RFS)均显著低于Ly+AML组(P<0.05)。 结论 与Ly+AML患者相比,MPAL患者的OS及RFS短,其预后不良可能与年龄、CD34高表达、Ph染色体阳性率高等因素有关。
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