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急性白血病的细胞遗传学研究。染色体失衡的预后意义。

Cytogenetic studies in acute leukaemias. Prognostic implications of chromosome imbalances.

作者信息

Alimena G, Annino L, Balestrazzi P, Montuoro A, Dallapiccola B

出版信息

Acta Haematol. 1977;58(4):234-9. doi: 10.1159/000207833.

Abstract

Consistent cytogenetic abnormalities have been detected in the bone marrow cells of 19 out of 33 patients (57.57%) with a recent diagnosis of acute leukaemia. Chromosome imbalances were apparently non-random, chromosomes 8, 17, 20 and 21 being more frequently involved. The median survival in the patients' group with abnormal metaphases was 55 vs. 210 days in patients with only normal metaphases. In the former group complete remission was obtained in 2 of 3 ALL patients and in 4 of 16 ANLL patients. Major karytypic abnormalities were consistently found in 5 subjects with EL. Peripheral blood culture lymphocytes showed a 9qh polymorphism in 2 of 35 patients and sporadic or consistent chromosome abnormalities in 6.

摘要

在最近诊断为急性白血病的33例患者中,有19例(57.57%)的骨髓细胞检测到一致的细胞遗传学异常。染色体失衡显然是非随机的,8号、17号、20号和21号染色体更常受累。中期异常的患者组中位生存期为55天,而中期仅正常的患者为210天。在前一组中,3例急性淋巴细胞白血病(ALL)患者中有2例、16例急性非淋巴细胞白血病(ANLL)患者中有4例获得完全缓解。在5例伴有嗜酸性粒细胞白血病(EL)的患者中始终发现主要核型异常。外周血培养淋巴细胞在35例患者中有2例显示9qh多态性,6例显示散发性或一致性染色体异常。

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