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慢性中性粒细胞白血病急变期与多发性骨髓瘤并存:一例报告及文献复习

Concurrent chronic neutrophilic leukemia blast crisis and multiple myeloma: A case report and literature review.

作者信息

Shi Jinning, Ni Ying, Li Jianyong, Qiu Hairong, Miao Kourong

机构信息

Department of Hematology, The Affiliated Jiangning Hospital, Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.

Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Hospital, Nanjing, Jiangsu 210029, P.R. China.

出版信息

Oncol Lett. 2015 May;9(5):2208-2210. doi: 10.3892/ol.2015.3043. Epub 2015 Mar 16.

Abstract

The current study presents the case of a 78-year-old male with concurrent chronic neutrophilic leukemia (CNL) and multiple myeloma (MM) who developed acute myeloid leukemia after two years of treatment with hydroxyurea, cyclophosphamide, prednisone and thalidomide. The patient presented with mature neutrophilic leukocytosis, hepatosplenomegaly, a high neutrophil alkaline phosphatase score and an absence of the Philadelphia chromosome or the BCR-ABL fusion gene. A bone marrow aspirate smear and biopsy indicated that the CNL coexisted with a plasma cell neoplasm. In addition, monoclonal λ-paraproteinemia was detected by serum protein immunofixation electrophoresis, and bone lesions were identified in multiple vertebrae. The patient achieved complete remission following one cycle of induction chemotherapy with the decitabine regimen in combination with the low-dose cytarabine, aclarubicin and granulocyte-colony stimulating factor (CAG) priming regimen. The occurrence of CNL and MM concurrently is extremely rare and thus, it has only been reported in a small number of cases. The occurrence of CNL and MM in the same patient as two distinct hematological malignancies indicates the neoplastic transformation of a pluripotent stem cell. Decitabine combined with the CAG priming regimen may present a good therapeutic strategy for elderly patients with secondary acute myeloid leukemia.

摘要

本研究报告了一例78岁男性患者,其同时患有慢性嗜中性粒细胞白血病(CNL)和多发性骨髓瘤(MM),在接受羟基脲、环磷酰胺、泼尼松和沙利度胺治疗两年后发展为急性髓系白血病。该患者表现为成熟嗜中性粒细胞增多、肝脾肿大、嗜中性粒细胞碱性磷酸酶评分高,且不存在费城染色体或BCR-ABL融合基因。骨髓穿刺涂片和活检表明CNL与浆细胞肿瘤共存。此外,血清蛋白免疫固定电泳检测到单克隆λ-副蛋白血症,多个椎体发现骨病变。该患者接受地西他滨方案联合低剂量阿糖胞苷、阿克拉霉素和粒细胞集落刺激因子(CAG)启动方案的一个诱导化疗周期后达到完全缓解。CNL和MM同时发生极为罕见,因此仅在少数病例中有报道。同一患者中CNL和MM作为两种不同的血液系统恶性肿瘤的发生表明多能干细胞发生了肿瘤转化。地西他滨联合CAG启动方案可能是老年继发性急性髓系白血病患者的一种良好治疗策略。

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