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Dacarbazine induced acute myeloid leukemia in melanoma.

机译:达卡巴嗪可诱发黑色素瘤急性髓性白血病。

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摘要

Treatment-related acute myeloid leukemia (tAML) is a rarely reported complication of therapy of melanoma. In fact, there are only four cases of tAML or myelodys-plastic syndrome (MDS) in chemotherapy treated melanoma patients reported in English literature. Two cases implicated either fotemustine or melphelan in secondary MDS or tAML [1,2]. A third case reported the combination of fotemustine and 'dacarbazine in association with tAML [3]. Only a single case report, from 1987, implicates single-agent dacarbazine in the development of myeloid leukemia in a melanoma patient [4]. In this case, the additional supporting information implicating the AML or MDS as a secondary process was not available. Cytogenetic analysis, while not essential in differentiating tAML from de novo AML, is still important to support the diagnosis of tAML. Here, we report a classic case of well-documented tAML secondary to dacarbazine, with a classic presentation including secondary trilineage dysplasia, and cytogenetics of tAML occurring secondary to previous alkylating agent therapy.
机译:与治疗有关的急性髓细胞性白血病(tAML)是黑色素瘤治疗的罕见报道并发症。实际上,在英文文献中仅报道了四例化疗治疗的黑色素瘤患者中的tAML或骨髓增生异常综合征(MDS)。继发性MDS或tAML中有2例涉及Fotemustine或melphelan [1,2]。第三例报道了将fotemustine和达达巴嗪与tAML联合使用[3]。自1987年以来,只有一例病例报告涉及单药达卡巴嗪与黑色素瘤患者骨髓性白血病的发生[4]。在这种情况下,暗示将AML或MDS作为辅助过程的其他支持信息不可用。细胞遗传学分析虽然在区分tAML和从头AML中不是必需的,但对于支持tAML的诊断仍然很重要。在这里,我们报道了达卡巴嗪继发的tAML经典案例,其中包括继发性三系发育异常和继发于先前烷化剂治疗的tAML细胞遗传学。

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