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[羟基脲治疗真性红细胞增多症后白血病转化及17号染色体异常]

[Leukemic transformation of polycythemia vera after treatment with hydroxyurea and chromosome 17 abnormalities].

作者信息

Tóthová E, Nebesnáková E, Kafková A, Stecová N, Fricová M

机构信息

Klinika hematológie LF UPJS, Kosice.

出版信息

Vnitr Lek. 1999 Aug;45(8):487-9.

Abstract

The authors present two patients with polycythemia vera where they recorded after several years' treatment with hydroxyurea development of acute myeloblastic leukaemia. In both instances they found, associated with leukaemia, abnormalities of chromosome no.17, in one case meeting criteria of the so-called 17p-syndrome. Progression of polycythemia vera into acute leukaemia is explained by the possible association with the long-term use of the drug and loss of chromosomal material (short arm of chromosome 17), the part where genes important in the process of leukaemogenesis are located. The authors draw attention to contemplated long-term administration of hydroxyurea to young patients with polycythemia vera. As cytogenetic analysis is a suitable method for evidence of progressing polycythemia vera into acute leukaemia, dynamic follow up of chromosomal changes is necessary, in particular in patients where long-term treatment with hydroxyurea is assumed.

摘要

作者报告了两名真性红细胞增多症患者,他们在用羟基脲治疗数年之后发生了急性髓细胞白血病。在这两个病例中,他们发现与白血病相关的17号染色体异常,其中一例符合所谓的17p综合征标准。真性红细胞增多症进展为急性白血病可解释为可能与长期使用该药物以及染色体物质(17号染色体短臂)缺失有关,而该区域存在白血病发生过程中重要的基因。作者提醒人们考虑对年轻的真性红细胞增多症患者长期使用羟基脲的问题。由于细胞遗传学分析是证明真性红细胞增多症进展为急性白血病的合适方法,因此有必要对染色体变化进行动态随访,尤其是对于那些假定长期接受羟基脲治疗的患者。

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