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成人急性淋巴细胞白血病的分型探讨
引用本文:Wang CC,Zhou CL,Wang HJ,Li QH,Liu XP,Gong BF,Liu BC,Lin D,Li W,Mi YC,Wang JX. 成人急性淋巴细胞白血病的分型探讨[J]. 中华血液学杂志, 2011, 32(7): 439-444. DOI: 10.3760/cma.j.issn.0253-2727.2011.07.002
作者姓名:Wang CC  Zhou CL  Wang HJ  Li QH  Liu XP  Gong BF  Liu BC  Lin D  Li W  Mi YC  Wang JX
作者单位:中国医学科学院、北京协和医学院血液学研究所、血液病医院,实验血液学国家重点实验室,天津,300020
基金项目:国家科技支撑计划课题,国家科技重大专项课题,公益性卫生行业科研专项课题
摘    要:目的 研究成人急性淋巴细胞白血病(ALL)生物学特征,分析WHO 2008年ALL分类的变化.方法 应用流式细胞术、R显带常规核型分析法、RT-PCR技术对初诊成人ALL患者进行免疫学、细胞遗传学、分子生物学检测.结果 ①共412例初诊成人ALL患者,男性239例,女性173例.免疫表型可分析病例410例,B系357例...

关 键 词:白血病,淋巴细胞,急性  免疫表型  细胞遗传学

Probe of classification of adult acute lymphoblastic leukemia
Wang Cui-Cui,Zhou Chun-Lin,Wang Hui-Jun,Li Qing-Hua,Liu Xu-Ping,Gong Ben-Fa,Liu Bing-Cheng,Lin Dong,Li Wei,Mi Ying-Chang,Wang Jian-Xiang. Probe of classification of adult acute lymphoblastic leukemia[J]. Chinese Journal of Hematology, 2011, 32(7): 439-444. DOI: 10.3760/cma.j.issn.0253-2727.2011.07.002
Authors:Wang Cui-Cui  Zhou Chun-Lin  Wang Hui-Jun  Li Qing-Hua  Liu Xu-Ping  Gong Ben-Fa  Liu Bing-Cheng  Lin Dong  Li Wei  Mi Ying-Chang  Wang Jian-Xiang
Affiliation:Institute of Hematology and Blood Diseases Hospital, CAMS and PUMC, Tianjin 300020, China.
Abstract:Objective To investigate the biologic features of adult acute lymphoblastic leukemia (ALL) ,and reclassified our ALL patients according to the 2008 WHO classification. Methods Immunophenotype and cytogenetic/molecular genetic results were obtained by flow cytometry, R-banding and RT-PCR,respectively. Results ① A total of 412 newly diagnosed and previously untreated adult ALL patients, were 239 males and 173 females. Among 410 patients with available immunophenotypic results, 357 were B-ALL and 53 T-ALL Myeloid antigen (MyAg) was higher expression in B-ALL than in T-ALL, and was correlated with the expression of CD34. ②93 Ph+ ALL patients, mainly CD10+ ALL, was associated with high WBC count and MyAg and CD34 expression. MLL rearrangement was found in 12 cases , mainly pro-B ALL .③299 cases could be analysed, according to the 2008 WHO classification of ALL, including 126 B-ALL with recurrent genetic abnormalities, and 120 B-ALL not otherwise specified. Among the 126 B-ALL with recurrent genetic abnormalities, 92 were Ph+ALL, 10 MLL + ALL, 11 hyperdiploid, 9 hypodiploid, 3 E2A-PBX+ , and 1 TEL-AML1 +. Patients with Ph+ , MLL+ , hypodiploid or E2A-PBX+ were associated with older age, higher WBC count, higher HGB, higher peripheral blasts and higher LDH level as compared with other patients.Conclusion Combination of immunophenotype and cytogenetic-molecular profiles can provide a further detailed classification of B-ALL.
Keywords:Leukemia,lymphocytic,acute  Immunophenotype  Cytogenetics
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