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米托蒽醌诱导的急性髓系白血病:病例报告

Acute myeloid leukaemia induced by mitoxantrone: case report.

作者信息

Arruda Walter Oleschko, Montú María Belén, de Oliveira Marcelo de Souza R, Ramina Ricardo

机构信息

Instituto de Neurologia de Curitiba, Curitiba PR, Brasil.

出版信息

Arq Neuropsiquiatr. 2005 Jun;63(2A):327-9. doi: 10.1590/s0004-282x2005000200024.

Abstract

Mitoxantrone (MX) is an immunosupressant drug used in secondarily progressive multiple sclerosis (SPMS) and in relapsing-remitting multiple sclerosis (RRMS). It has a leukemogenesis potential induced by cytogenetic abnormalities, though with a low incidence. Promyelocitic leukaemia (type M3) and other forms of acute myeloblastic leukaemias (M4 and M5) have been described in a few MS patients who received MX during their treatment. We describe a white female patient, 47 year-old, with SPMS (EDSS = 4) with 14 years of disease. She received MX during her disease and developed acute promyelocytic leukaemia (M3), with severe thrombocytopenia 30 months later. She ultimately died due to intracerebral hemorrhage. Other cases of treatment related to AML are reviewed and discussed.

摘要

米托蒽醌(MX)是一种免疫抑制剂药物,用于继发进展型多发性硬化症(SPMS)和复发缓解型多发性硬化症(RRMS)。它具有由细胞遗传学异常诱导的白血病发生潜能,尽管发生率较低。在少数治疗期间接受MX的MS患者中,已经描述了早幼粒细胞白血病(M3型)和其他形式的急性髓细胞白血病(M4和M5)。我们描述了一名47岁的白人女性患者,患有14年病史的SPMS(扩展残疾状态量表评分=4)。她在患病期间接受了MX治疗,并在30个月后发展为急性早幼粒细胞白血病(M3),伴有严重血小板减少症。她最终因脑出血死亡。对其他与急性髓细胞白血病相关的治疗病例进行了回顾和讨论。

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