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[伴有双微体染色体的急性髓系白血病患者经标准诱导治疗后完全缓解]

[Complete remission after standard induction therapy in a patient with acute myeloid leukemia associated with double-minute chromosomes].

作者信息

Goto Miyo, Fukushima Nobuaki, Iida Shiori, Ito Makoto, Kawamura Yuma, Ukai Shun, Sagou Ken, Fukuyama Ryuichi, Kohno Akio, Ozeki Kazutaka

机构信息

Department of Hematology/Oncology, Konan Kosei Hospital.

Department of Pathology, Konan Kosei Hospital.

出版信息

Rinsho Ketsueki. 2021;62(4):245-250. doi: 10.11406/rinketsu.62.245.

Abstract

Acute myeloid leukemia (AML) associated with double-minute chromosomes (dmin) is a rare condition and has a poor prognosis. A 68-year-old man with leukocytosis and thrombocytopenia was admitted to our hospital. Bone marrow aspiration showed that 79.5% of myeloblasts were positive for myeloperoxidase. The patient was diagnosed with acute myeloid leukemia (French-American-British classification: M2, World Health Organization classification: AML, not otherwise specified, AML with maturation). Chromosomal analysis revealed the presence of dmin: 45, X, -Y, 5-33 dmin. Fluorescence in situ hybridization revealed multiple MYC signals, and spectral karyotyping showed that dmin was derived from chromosome 8. These findings indicated resistance to chemotherapy alone. After the standard induction therapy with daunorubicin and cytarabine, the number of myeloblasts in the bone marrow decreased, and the amplified MYC signals disappeared. Then, the patient achieved complete remission. Reportedly, most patients with AML correlated with dmin have a complex karyotype, except for this case. Owing to the absence of a complex karyotype, the patient had good sensitivity to chemotherapy. Further studies with a larger population of patients with AML associated with dmin, but without complex karyotypes, should be conducted to accurately predict prognosis in such cases.

摘要

与双微体染色体(dmin)相关的急性髓系白血病(AML)是一种罕见疾病,预后较差。一名患有白细胞增多症和血小板减少症的68岁男性入住我院。骨髓穿刺显示79.5%的成髓细胞髓过氧化物酶呈阳性。该患者被诊断为急性髓系白血病(法美英分类:M2,世界卫生组织分类:AML,未另行指定,伴成熟的AML)。染色体分析显示存在dmin:45,X,-Y,5-33 dmin。荧光原位杂交显示多个MYC信号,光谱核型分析表明dmin源自8号染色体。这些发现提示单纯化疗耐药。在用柔红霉素和阿糖胞苷进行标准诱导治疗后,骨髓中的成髓细胞数量减少,扩增的MYC信号消失。随后,患者实现完全缓解。据报道,除该病例外,大多数与dmin相关的AML患者具有复杂核型。由于不存在复杂核型,该患者对化疗具有良好的敏感性。应开展针对更多无复杂核型的与dmin相关的AML患者的进一步研究,以准确预测此类病例的预后。

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