Unmasking of Chronic Myelomonocytic Leukemia after Treatment of Chronic Lymphocytic Leukemia with Rituximab

Lesley N. Bobek , Jason K. Hyde , Keith S. Hansen
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引用次数: 1

Abstract

The association of myelodysplastic syndromes with lymphoid malignancies has rarely been reported. To our knowledge, there are only 5 reported cases of chronic lymphocytic leukemia (CLL) and chronic myelomonocytic leukemia (CMML) occurring in the same patient. Herein, we describe the case of an 80-year-old woman diagnosed with CLL. She declined chemotherapy and began weekly rituximab 375 mg/m2 intravenously. She initially had a solid partial response to treatment. However, after 2 treatments with rituximab her white blood cell count increased, and a peripheral smear was remarkable for large, cleaved, folded cells, identified as monocytes. The previous bone marrow biopsy was retrieved and restained with an α-naphthol butyl esterase for monocytes. An increased atypical monocytic population was exposed, indicative of an evolving CMML. Her 2 malignancies probably arose from 2 different clones by chance. Treatment was begun with decitabine, but with no response. The patient remains transfusion dependent although relatively asymptomatic on hydroxyurea.

利妥昔单抗治疗慢性淋巴细胞白血病后慢性髓单细胞白血病的揭示
骨髓增生异常综合征与淋巴系统恶性肿瘤的关联很少被报道。据我们所知,仅有5例慢性淋巴细胞白血病(CLL)和慢性髓细胞白血病(CMML)同时发生在同一患者身上。在此,我们描述一个80岁的妇女诊断为慢性淋巴细胞白血病的情况。她拒绝化疗,开始每周静脉注射美罗华37mg /m2。她最初对治疗有一定的部分反应。然而,经过2次利妥昔单抗治疗后,她的白细胞计数增加,外周涂片上有明显的大的、分裂的、折叠的细胞,鉴定为单核细胞。取之前的骨髓活检,用α-萘酚丁基酯酶对单核细胞进行抑制。暴露的非典型单核细胞群体增加,表明CMML正在发展。她的两种恶性肿瘤可能是偶然从两个不同的克隆体中产生的。治疗开始使用地西他滨,但没有反应。患者仍然依赖输血,虽然羟基脲相对无症状。
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