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对两种可能由苯诱发的罕见恶性血液疾病进行染色体分析。

Chromosome analysis in two unusual malignant blood disorders presumably induced by benzene.

作者信息

Van den Berghe H, Louwagie A, Broeckaert-Van Orshoven A, David G, Verwilghen R

出版信息

Blood. 1979 Apr;53(4):558-66.

PMID:426907
Abstract

Two patients with presumably benzene-induced malignant blood disorders with preleukemic phases were cytogenetically monitored through the courses of their diseases. Patient 1, in addition to a familial chromosome translocation [t(3;16)], developed karyotypic abnormalities in 100% of the marrow cells, including two translocation: t(9;16)] and t(4;15). Monosomy of chromosome 7 characterized the cells of patient 2. Cytogenetic monitoring of the patients at various phases of their diseases served as an important indicator of the transformation or progression of the preleukemia into frank leukemia and of the unusual behavior of such leukemic cells.

摘要

对两名疑似患有苯诱导的恶性血液疾病且处于白血病前期的患者在其病程中进行了细胞遗传学监测。患者1除了有家族性染色体易位[t(3;16)]外,100%的骨髓细胞出现了核型异常,包括两种易位:t(9;16)和t(4;15)。7号染色体单体是患者2细胞的特征。在患者疾病的不同阶段进行细胞遗传学监测,是白血病前期转变为明显白血病以及此类白血病细胞异常行为的重要指标。

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