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Development of acute lymphoblastic leukemia following treatment for acute myeloid leukemia in children with Down syndrome: A case report and retrospective review of Children's Oncology Group acute myeloid leukemia trials

机译:急性淋巴细胞白血病治疗急性淋巴细胞白血病患儿患儿综合征的急性髓白血病:一种案例报告及对儿童肿瘤群急性髓性白血病试验的案例报告及回顾述评

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Abstract Children with Down syndrome have a 150‐fold increased risk of developing acute myeloid leukemia (AML) and 20‐fold increased risk of developing acute lymphoblastic leukemia (ALL). Although the risk of developing AML and ALL is significantly increased in children with Down syndrome, the development of both malignancies in the same patient is very rare. We describe a patient with Down syndrome who developed ALL 6 years after being diagnosed with AML. We performed a literature review and Children's Oncology Group query and discovered eight published cases and five cases of ALL following AML in pediatric patients with Down syndrome, as well as six cases of ALL following AML in non‐Down syndrome patients. There was a similar cumulative incidence of ALL after treatment for AML in the Down syndrome and non‐Down syndrome populations. Overall survival in patients with Down syndrome who developed ALL after treatment for AML was comparable to overall survival for patients with Down syndrome with de novo ALL with an average follow‐up of 7 years after ALL diagnosis. Clinical data collected were used to discuss whether this phenomenon represents a secondary leukemia, second primary cancer, or mixed‐lineage leukemia.
机译:患有唐氏综合症的抽象儿童增加了发育急性髓性白血病(AML)的风险增加150倍,增加了急性淋巴细胞白血病(ALL)的20倍。虽然在患有综合症的儿童中发育AML和所有的风险显着增加,但同一患者的恶性肿瘤的发展是非常罕见的。我们描述了患有唐氏综合症的患者,他们在被诊断患有AML后开发了6年。我们进行了文献综述和儿童肿瘤学群查询,发现了八个发表的病例,并在小儿综合征患者中进行了患者的八种情况,以及患有综合症患者的六种情况下的六种病例。在唐氏综合征和非衰减综合征群体中治疗AML的所有累积发生率。患有唐氏综合症患者的患者的总生存率在治疗AML后的整体存活率与De Novo患者的患者的整体存活率相当,并且在所有诊断后7年的平均随访。收集的临床数据用于讨论这种现象是代表次生白血病,第二原癌症或混合血型白血病。

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