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A retrospective analysis of thirty-one cases of plasma cell leukemia from a single center in China.

机译:回顾性分析来自中国一个中心的31例浆细胞白血病。

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BACKGROUND/AIMS: The study was undertaken to understand the characteristic of plasma cell leukemia (PCL) in China. METHODS: We reviewed and compared medical data of 22 primary PCL, 9 secondary PCL and 461 multiple myeloma (MM) diagnosed at our institute from January 2000 to January 2008. RESULTS: The median onset ages of primary and secondary PCL patients were 49.5 and 56 years, respectively. PCL patients presented with a low peripheral blood plasmacytosis, extensive involvement of visceral organs and poor residual bone marrow function, without severe renal insufficiency. Seventeen of twenty-one PCL patients had abnormal karyotypes, mostly complex and hypodiploid or pseudodiploid. The deletion of 13q was frequent in primary and secondary PCL (57.1 and 42.9%, respectively). There was a significant difference in survival among primary PCL, secondary PCL and MM (median 14, 2 and 37 months, respectively, p = 0.0000). CONCLUSION: Overall, primary and secondary PCL are different disorders with distinct natural histories and survival.
机译:背景/目的:该研究旨在了解中国浆细胞白血病(PCL)的特征。方法:我们回顾并比较了我院2000年1月至2008年1月诊断的22例原发性PCL,9例继发性PCL和461例多发性骨髓瘤(MM)的临床资料。结果:原发性和继发性PCL患者的中位发病年龄分别为49.5和56年。 PCL患者的外周血浆细胞增多症低,内脏器官广泛受累,剩余骨髓功能差,没有严重的肾功能不全。 21名PCL患者中有17名具有异常的染色体核型,多数为复杂的二倍体或假二倍体。在原发性和继发性PCL中13q的缺失很常见(分别为57.1%和42.9%)。原发性PCL,继发性PCL和MM之间的生存率存在显着差异(分别为中位数14、2和37个月,p = 0.0000)。结论总体而言,原发性和继发性PCL是不同的疾病,具有不同的自然历史和生存率。

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