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首页> 外文期刊>British Journal of Cancer >Cytogenetic study in therapy-related myelodysplastic syndromes (t-MDS) and acute non-lymphocytic leukaemia (t-ANLL)
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Cytogenetic study in therapy-related myelodysplastic syndromes (t-MDS) and acute non-lymphocytic leukaemia (t-ANLL)

机译:治疗相关的骨髓增生异常综合症(t-MDS)和急性非淋巴细胞性白血病(t-ANLL)的细胞遗传学研究

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A cytogenetic study was performed in 27 patients suspected of t-MDS or t-ANLL. In 12 patients the diagnosis of t-MDS or t-ANLL was confirmed by morphological, cytochemical and immunophenotypical analysis. The cases were classified as RA (one), RAEB (four), CMML (two), ANLL (five). They had received chemotherapy and/or RT for Hodgkin's disease (eight cases), solid tumours (three cases) and multiple myeloma (one case). Clonal chromosome abnormalities were found in bone marrow or peripheral blood cells in all the 12 cases. Five patients had a clonal abnormality of chromosome no. 5 (monosomy, deletions, translocation and inversion of 5q). The critical region on chromosome no. 5 comprised bands q12-q34. Monosomy and deletion of chromosome 7q was observed in the other two patients. In the six remaining patients various karyotypic patterns were observed including a t(4;11) (q21;q23) in one case, monosomies (four cases) and trisomies (one case) of different chromosomes. In the other 15 cases, the presence of a normal karyotype together with the morphological and immunophenotypical characterisation was consistent with a diagnosis of non-neoplastic specimens.
机译:在27名怀疑患有t-MDS或t-ANLL的患者中进行了细胞遗传学研究。通过形态学,细胞化学和免疫表型分析证实了12例患者中t-MDS或t-ANLL的诊断。病例分为RA(1例),RAEB(4例),CMML(2例),ANLL(5例)。他们接受了霍奇金病(8例),实体瘤(3例)和多发性骨髓瘤(1例)的化疗和/或放疗。在所有12例中,在骨髓或外周血细胞中发现克隆染色体异常。 5例患者克隆号为染色体异常。 5(单性,5q的缺失,易位和倒置)。染色体上的关键区域5个包括频带q12-q34。在其他两名患者中观察到了单染色体切割和染色体7q缺失。在剩下的六名患者中,观察到各种核型,包括在一种情况下的t(4; 11)(q21; q23),不同染色体的单染色体性(4例)和三体性(1例)。在其他15例中,正常核型的存在以及形态和免疫表型特征与非肿瘤标本的诊断是一致的。

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