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缺血性中风作为慢性髓性白血病早幼粒细胞急变期的首发特征——一种罕见的表现:伊马替尼时代后的病例报告及文献综述

Ischemic stroke as a presenting feature of promyelocytic blast phase in chronic myeloid leukemia - an uncommon presentation: a case report and literature review in the post imatinib era.

作者信息

Tripathi Swapnil, K V Vinu Balraam, Nayak Amiya Ranjan, Chauhan Richa, Kumar Pradeep, Dass Jasmita, Naranje Priyanka, Aggarwal Mukul

机构信息

Department of Hematology, All India Institute of Medical Sciences, New Delhi, India.

Department of Radiodiagnosis and Intervention Radiology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Ann Hematol. 2024 Dec;103(12):6007-6013. doi: 10.1007/s00277-024-06044-9. Epub 2024 Oct 16.

Abstract

Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm (MPN characterized by reciprocal translocation in the ABL1 and BCR region of chromosomes 9 and 22 respectively. Progression to the blast phase in chronic myeloid leukemia results in a poorer prognosis. It can be of either myeloid, lymphoid or a mixed lineage. Progression to the promyelocytic blast phase is very rare, and there are no evidence-based guidelines for its management. Thrombosis in CML is not well defined. Thrombosis can be seen in patients with acute promyelocytic leukemia (APL) with venous thrombosis (VTE) being more common than arterial thrombosis. Ischemic stroke as the presenting feature of blast phase progression in CML is extremely rare. We report a case of CML who presented to us with acute ischemic stroke and subsequently was diagnosed as CML transformed to the promyelocytic blast phase. She was successfully treated with dasatinib along with all-trans retinoic acid (ATRA) and arsenic trioxide (ATO).

摘要

慢性髓性白血病(CML)是一种骨髓增殖性肿瘤(MPN),其特征是分别在9号和22号染色体的ABL1和BCR区域发生相互易位。慢性髓性白血病进展为急变期会导致预后较差。它可以是髓系、淋系或混合谱系。进展为早幼粒细胞急变期非常罕见,且尚无基于证据的管理指南。CML中的血栓形成尚无明确定义。在急性早幼粒细胞白血病(APL)患者中可见血栓形成,静脉血栓形成(VTE)比动脉血栓形成更常见。以缺血性卒中作为CML急变期进展的首发特征极为罕见。我们报告1例CML患者,该患者因急性缺血性卒中就诊,随后被诊断为CML转化为早幼粒细胞急变期。她接受达沙替尼联合全反式维甲酸(ATRA)和三氧化二砷(ATO)治疗成功。

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