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作 者:沈军[1] 马亮[1] 钟明华[2] 韩呈武[1] 曹永跃[1] 湛玉良[1] 曹永彤[1]
机构地区:[1] 中日友好医院检验科,北京100029 [2] 中日友好医院血液科,北京100029
出 处:《现代检验医学杂志》2014年第2期130-133,共4页Journal of Modern Laboratory Medicine
摘 要:目的 分析伴t(8;21)易位急性髓细胞初诊白血病患者FAB分型、血常规、骨髓细胞形态学、细胞遗传学及临床预后特点.方法 20例患者为中日友好医院2004年-2011年按WHO标准确诊的急性髓细胞白血病(AML)患者,血常规采用XE-2100全自动分析仪分析;骨髓细胞形态学检测对骨髓涂片进行瑞氏-姬姆萨染色,显微镜计数细胞;细胞遗传学检测为常规培养骨髓细胞,采用G显带技术对染色体核型进行分析.结果 伴t(8;21)易位AML患者中55%(11/20)患者外周血白细胞升高,20%(4/20)患者白细胞减低,所有患者均伴血小板减低.85%(17/20)患者骨髓涂片中可见奥氏小体.根据FAB分型,20例患者中15%(3/20)诊断为MDS-RAEB,20%(4/20)为MDS-RAEBt,55%(11/20)为AML-M2,10%(2/10)为AML-M4.55%(11/20)患者为单纯t(8;21)易位,45%(9/20)患者为t(8;21)易位同时伴有其它异常,其中伴性染色体丢失占所有患者35%(7/20),伴有9q-占所有患者的10%(2/20).82.4%(14/17)患者能达到完全缓解.结论 伴t(8;21)易位AML患者可见于FAB分型的不同亚型,主要见于AML-M2.t(8;21)患者常伴有附加异常,以性染色体丢失常见.t(8;21)易位患者疗效较好.Objective To study the features of the FAB subgroups, blood routine, morphologic, cytogenetic and prognosis in deno acute myeloid leukemia(AML) patients with t(8;21). Methods 20 patients from 2004 to 2011 were diagnosed by WHO criterion,blood routine were analyzed by XE-2100 auto analyzer. Morphologic were stained by Wright' s-Giemsa,and counted by microscope. The chromosome was prepared with brief culture of bone marrow,and the karyotype was analyzed by G banding technique. Results The number of white cell in 55 % of the AML patients with t(8;21) were higher than nor real,and 20 % patients were lower than normal, the platelet count of all the patients were lower. Auer body could be detected in 85 % patients (17/20). According FAB subgroups, 15% (3/20) patients could be diagnosed as MDS-RAEB, 20% (4/20) patients were MDS-RAEBt,55%(11/20) were AML-M2,and 10%(2/10) were AML-M4.55%(11/20) patients were t(8; 21) without other additional aberrations, 45 % (9/20) patients were t (8 ; 21) with other additional aberrations. Sex chromosome losses were found in 35%(7/20) patients,and 9q were found in 10%(2/20) patients. 82.4%(14/17) patients could achieve complete remission. Conclusion The acute myeloid leukemia patients with t(8;21) could be detected in different sub groups according FAB,mainly distributed in AML-M2. The t(8;21) AML patients often had many other additional aberrations,and sex chromosome losses were common. The efficacy of t(8;21) patients were better.
分 类 号:R551[医药卫生—血液循环系统疾病]
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