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A Retrospective Analysis of Thirty-One Cases of Plasma Cell Leukemia from a Single Center in China

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<i>Background/Aims:</i> The study was undertaken to understand the characteristic of plasma cell leukemia (PCL) in China. <i>Methods:</i> 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. <i>Results:</i> 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). <i>Conclusion:</i> Overall, primary and secondary PCL are different disorders with distinct natural histories and survival.
Title: A Retrospective Analysis of Thirty-One Cases of Plasma Cell Leukemia from a Single Center in China
Description:
<i>Background/Aims:</i> The study was undertaken to understand the characteristic of plasma cell leukemia (PCL) in China.
<i>Methods:</i> 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.
<i>Results:</i> 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).
<i>Conclusion:</i> Overall, primary and secondary PCL are different disorders with distinct natural histories and survival.

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