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Updated: Jun 8, 2025

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血液瘤中的PICALM-MLLT10融合基因:临床特征,当前实践和预后

Ji-Nuo Wang1,2,3, Bangcheng Ye1, Fei Cheng4

  • 1Bone Marrow Transplantation Center of The First Affiliated Hospital & Liangzhu Laboratory, Zhejiang University School of Medicine, Hangzhou, People's Republic of China.

Hematology (Amsterdam, Netherlands)
|November 5, 2024
PubMed
概括

在亚洲血性恶性瘤中,PICALM-MLLT10融合基因是罕见的. 被诊断出这种基因的患者,包括急性髓性白血病和急性淋巴细胞白血病,预后和生存率不佳.

关键词:
这就是PICALM-MLLT10的原因.急性淋巴细胞白血病急性淋巴细胞白血病急性骨髓性白血病 (AML) 是一种急性骨髓性白血病.融合基因 融合基因 融合基因混合现象型急性白血病混合现象型急性白血病

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