髓性白血病
医学
单体
急性早幼粒细胞白血病
肿瘤科
髓样
内科学
免疫学
癌症研究
核型
染色体
生物
维甲酸
遗传学
基因
作者
Simona Zompì,Olivier Legrand,Didier Bouscary,Claude Blanc,Françoise Picard,Nicole Casadevall,F. Dreyfus,Jean‐Pierre Marie,F Viguié
标识
DOI:10.1046/j.1365-2141.2000.02240.x
摘要
We describe two patients with positive t(15;17) acute promyelocytic leukaemia (APL) that developed into a therapy-related myelodysplasia 2-2.5 years after complete remission (CR) and then evolved into therapy-related acute myeloid leukaemia (t-AML). Both patients received anthracyclines as potential leukaemogenic drugs. In both cases, cytogenetic changes usually occurring after use of alkylating agents were noticed: monosomy 7 associated with monosomy 5 or 5q- chromosome. A review of the literature on t-AML occurring after successful therapy for APL showed only one report similar to these two cases. These observations suggest that anthracyclines can cause t-AML similar to that induced by alkylating agents.
科研通智能强力驱动
Strongly Powered by AbleSci AI