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Acute Myeloid Leukemia with Philadelphia Chromosome, Near-tetraploidy, and 5q Deletion

机译:急性髓性白血病与费城染色体,近四倍体和5季度删除

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A 49-year-old male presented to his physician with three weeks of dyspnea, dry cough, and fever. He did not respond to antibiotics and corticosteroids. He presented to the emergency department with worsening symptoms, where blood work revealed severe anemia, leukocytosis, thrombocytopenia, and 61% blasts on peripheral smear. Bone marrow biopsy showed acute myeloid leukemia (AML). While the results of other studies were awaited, treatment was begun with 7+3 induction (cytarabine and daunorubicin). Karyotyping returned?positive for the BCR-ABL1 fusion gene (Philadelphia chromosome), near-tetraploidy, and 5q deletion. Follow-up bone marrow biopsy revealed residual disease (12% blasts). Re-induction was initiated with 5+2 cytarabine and daunorubicin with the addition of dasatinib. Subsequent bone marrow biopsies revealed minimal residual disease and BCR-ABL on polymerase chain reaction (PCR). The patient was placed on dasatinib maintenance and later switched to nilotinib. This case demonstrates the simultaneous presence of rare cytogenetic abnormalities in AML. It also discusses the successful utilization of tyrosine kinase inhibitors (TKIs) in the treatment of BCR-ABL-positive AML, as there are no established guidelines.
机译:一个49岁的男性向他的医生展示,伴有了三周的呼吸困难,干咳和发烧。他没有反应抗生素和皮质类固醇。他向急诊院提交了恶化的症状,血液工作揭示了严重的贫血,白细胞增多症,血小板减少症和周围涂片的61%爆炸。骨髓活检显示急性髓性白血病(AML)。虽然等待了其他研究的结果,但是患有7 + 3诱导(月曲和Daunorubicin)的治疗。核型化返回了BCR-ABL1融合基因(费城染色体),近四倍体和5Q缺失的阳性。随访的骨髓活检显示残留疾病(12%爆炸)。用加入达沙替尼用5 + 2个月曲和DaUnorubic引发重新诱导。随后的骨髓活组织检查显示了聚合酶链反应(PCR)上的最小残余疾病和BCR-ABL。将患者置于Dasatinib维护上,后来切换到Nileotinib。本例证明了AML中罕见细胞遗传学异常的同时存在。它还讨论了酪氨酸激酶抑制剂(TKI)治疗BCR-Abl阳性AML的成功利用,因为没有建立的准则。

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