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作 者:周瑞莲[1] 莫耀禧[2] 蓝梅[1] 林金盈[1]
机构地区:[1]广西壮族自治区人民医院血液内科,南宁市530021 [2]广西壮族自治区人民医院生殖医学与遗传中心,南宁市530021
出 处:《广西医学》2012年第3期275-278,共4页Guangxi Medical Journal
基 金:广西医药卫生科研课题(桂卫Z2008057;桂卫Z2009133)
摘 要:目的探讨FISH法检测PML-RARa融合基因在急性早幼粒细胞白血病(APL)中的临床应用价值。方法对21例疑诊APL患者应用FISH技术检测PML-RARa融合基因。结果 21例疑诊患者中最后确诊为APL 15例,排除APL 6例。15例APL患者中PML-RARa融合基因阳性14例,PML-RARa融合基因阴性者1例,该患者经最后确诊为APL变异型,经诱导治疗后效果不佳。6例疑诊患者PML-RARa融合基因均为阴性,确诊为急性髓细胞白血病-M2。结论 FISH法检测PML-RARa融合基因敏感、可靠,对APL的确诊及指导治疗有重要价值。Objective To investigate the application of fluorescence in situ hybridization (FISH) for the detection of PML-RARa fusion gene in the diagnosis and treatment of acute promyelocytic leukemia(APL). Methods PML-RARa fusion gene detection was performed in 21 patients suspected of APL by FISH. Results Of the 21 suspected APL patients, fifteen cases were eonfirrned of APL. Positive PML-RARa fusion genes were found in 14 of the 15 APL patients,while one ease with negative PML-RARa fusion gene was confirmed to be variant APL and was treated with all-trans retinoie acid (ATRA)-induction therapy but the effieacy was poor. The remaining 6 suspected APL patients with negative PML-RARa fusion gene were eonfirmed to be acute myeloid leukemia-M2. Conclusion Detection of PML-RARa fusion gene by FISH is sensitive and reliable, and is of great value for the diagnosis and treatment of APL.
关 键 词:急性早幼粒细胞白血病 荧光原位杂交 PML-RARa融合基因
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