Acute monocytic leukemia with translocation t(1;11) (p31;q23): simultaneous staining of chromosomes and cell surface antigens.

I Nölle, B Schlegelberger, N Schmitz, S Bödewadt-Radzun, W Grote
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引用次数: 5

Abstract

Cytogenetic analysis of leukemic cells from a 76-year-old patient with acute monocytic leukemia revealed the karyotype 47,XY, +8,t(1;11)(p31;q23). To the best of our knowledge this is the first case with involvement of the short arm of chromosome 1 in a t(1;11) in acute nonlymphocytic leukemia. In order to determine which hematopoietic cell lineages are involved in this case, we used a method to demonstrate chromosomes and cell surface antigens of the same cell. To identify mitoses as monocytic, erythrocytic, megakaryocytic, or lymphocytic, cell surface antigens were stained with monoclonal antibodies in an APAAP detection procedure. Subsequently, an R-banding technique was performed. About 80% of the abnormal mitoses expressed monocytic markers. No erythrocytic, megakaryocytic, or lymphocytic mitoses were found. Only an involvement of the monocytic cell lineage was revealed.

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急性单核细胞白血病易位t(1;11) (p31;q23):染色体和细胞表面抗原同时染色。
对76岁急性单核细胞白血病患者白血病细胞的细胞遗传学分析显示核型为47,XY, +8,t(1;11)(p31;q23)。据我们所知,这是在急性非淋巴细胞白血病中第一例涉及1号染色体短臂的病例(1;11)。为了确定哪一种造血细胞系参与了这种情况,我们使用了一种方法来展示同一细胞的染色体和细胞表面抗原。为了鉴别单核细胞、红细胞、巨核细胞或淋巴细胞的有丝分裂,在apap检测程序中,用单克隆抗体对细胞表面抗原进行染色。随后,进行r带技术。约80%的异常有丝分裂表达单核细胞标记物。未见红细胞、巨核细胞或淋巴细胞有丝分裂。只有单核细胞谱系的参与被揭示。
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Acute monocytic leukemia with translocation t(1;11) (p31;q23): simultaneous staining of chromosomes and cell surface antigens. Preliminary results of intensive therapy of children and adolescents with acute nonlymphocytic leukemia--a Childrens Cancer Study Group report. Remission induction and postremission therapy in acute myelogenous leukemia: British MRC Study. A randomized comparison of intensive maintenance treatment for adult acute myelogenous leukemia using either cyclic alternating drugs or repeated courses of the induction-type chemotherapy: AML-6 trial of the EORTC Leukemia Cooperative Group. Pretherapeutic drug testing in acute leukemias for prediction of individual prognosis.
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