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Long-term colchicine therapy in a patient with Beh?et’s disease and acute promyelocytic leukemia

机译:Beh?et病和急性早幼粒细胞白血病患者的长期秋水仙碱治疗

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Beh?et’s disease causes a continuous T-lymphocytic mediated inflammatory reaction in the small arterioles, which results in gradual destruction of any human organ or system. The benefit of treatment with colchicine in patients with Beh?et’s disease has been reported in literature. Acute leukemia has seldom been associated with Beh?et’s disease, although acute promyelocytic leukemia is a particular subtype of leukemia that is often characterized by special cytogenetic abnormalities. We report a male patient with acute promyelocytic leukemia and Beh?et’s disease who had received long-term treatment with colchicine. To our knowledge, this is the first report of the concomitant occurrence of acute promyelocytic leukemia and Beh?et’s disease, which suggests that long-term colchicine therapy has a role in the pathogenesis of acute promyelocytic leukemia. The patient described has been treated with retinoic acid and idarubicin (the ATRA-IDA protocol). At the time of this writing, his disease is in clinical remission.
机译:贝赫耶特氏病引起小动脉中持续的T淋巴细胞介导的炎症反应,导致任何人体器官或系统的逐渐破坏。文献已经报道了用秋水仙碱治疗贝希特氏病的益处。尽管急性早幼粒细胞白血病是一种特殊的白血病亚型,通常以特殊的细胞遗传学异常为特征,但急性白血病很少与贝希特氏病相关。我们报道了一名长期接受秋水仙碱治疗的患有急性早幼粒细胞白血病和贝希特氏病的男性患者。据我们所知,这是急性早幼粒细胞白血病与贝赫特氏病并发的首次报道,这表明长期秋水仙碱治疗在急性早幼粒细胞白血病的发病机理中具有重要作用。所述患者已接受视黄酸和达柔比星治疗(ATRA-IDA方案)。在撰写本文时,他的病正在临床缓解中。

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