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B-Lymphoid and myeloid lineages biphenotypic acute leukemia with t(8;21)(q22;q22)
Authors:Guangsheng He  Depei Wu  Aining Sun  Yongquan Xue  Zhengming Jin  Huiying Qiu  Xiaowen Tang  Miao Miao  Zhengzheng Fu  Xiao Ma  Xiuli Wang  Zixin Chen  Changgeng Ruan
Institution:(1) Jiangsu Insititute of Hematology, First Affiliated Hospital of Soochow University, Suzhou, 215006, Jiangsu, People’s Republic of China
Abstract:By analyzing the characteristics of morphology, immune phenotype, chromosome karyotype and clinical manifestations of six cases of B-lymphoid and myeloid lineages biphenotypic acute leukemia (BAL) with t(8;21)(q22;q22), a new subgroup of BAL was reported. Bone marrow eosinophilia (more than 5%) and pseudo-Chediak abnormalities were not found. Auer rods were also not identified in four of six cases. Immunophenotype revealed B-lymphoid and myeloid lineages positive, together with frequent and high expression of CD34 and CD33, and weak expression of HLA-DR. In addition to t(8;21) chromosomal translocation, deletion of Y chromosome and complex chromosome abnormalities were also found. Chemotherapy for myeloid and lymphoid leukemia simultaneously produced good response in the patients. BAL with t(8; 21)(q22; q22) might be a new subgroup of BAL, and it was suggested that the leukemia clone with t(8;21)(q22;q22) might have originated from an early phase of hematopoiesis, and AML1/ETO fusion gene might be related to differentiation of B lymphocyte.
Keywords:Leukemia  Biphenotypic  Acute  t(8  21)(q22  q22)  AML1/ETO
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