Rapid transformation of chronic lymphocytic leukemia to acute lymphoblastic leukemia: A rare case report

Manmeet Kaur, Sarita Nibhoria, K. Tiwana, A. Bajaj, S. Chhabra
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引用次数: 5

Abstract

Chronic lymphocytic leukemia (CLL) is characterized by the accumulation of mature-appearing lymphocytes in blood, bone marrow, lymph nodes, and spleen with a median lymphocyte count of 20–30 × 109/L at the time of diagnosis. In half of the patients, the lymphocyte count doubles over a period of 1-year and cyclic rise up to 50 × 109/L can occur in untreated patients while in others the count may remain stable for years. Based on the cytogenetic and molecular studies, it has been demonstrated that multiple clones may occur in CLL and clonal evolution is a frequent occurrence. The transformation of CLL to a high-grade non-Hodgkin's lymphoma such as diffuse large B cell lymphoma, Hodgkin lymphoma, and prolymphocytic leukemia is well documented. Whereas the transformation of CLL to acute leukemia occurs in <1% cases and this contrasts the almost invariable progression in patients with chronic myeloid leukemia. Here, we report a rare case of a 55-year-old lady, a diagnosed case of CLL transforming into B-cell acute lymphocytic leukemia over a very short interval of 1 week period.
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慢性淋巴细胞白血病迅速转化为急性淋巴细胞白血病:罕见病例报告
慢性淋巴细胞白血病(Chronic lymphocytic leukemia, CLL)以血液、骨髓、淋巴结和脾脏中出现成熟淋巴细胞积累为特征,诊断时淋巴细胞中位数为20 ~ 30 × 109/L。在一半的患者中,淋巴细胞计数在1年内翻倍,未经治疗的患者循环上升至50 × 109/L,而在其他患者中,计数可能保持稳定数年。基于细胞遗传学和分子生物学的研究表明,CLL可能存在多个克隆,克隆进化是一个频繁发生的过程。CLL向高级别非霍奇金淋巴瘤(如弥漫性大B细胞淋巴瘤、霍奇金淋巴瘤和前淋巴细胞白血病)的转变有充分的文献记载。然而,CLL向急性白血病的转化发生在<1%的病例中,这与慢性髓性白血病患者几乎不变的进展形成对比。在此,我们报告一个罕见的病例,一位55岁的女性,诊断为CLL转化为b细胞急性淋巴细胞白血病,时间间隔很短,只有1周。
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