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Published in: International Journal of Hematology 3/2009

01-04-2009 | Review Article

Plasma cell leukemia: a highly aggressive monoclonal gammopathy with a very poor prognosis

Authors: Victor H. Jimenez-Zepeda, Virginia J. Dominguez-Martinez

Published in: International Journal of Hematology | Issue 3/2009

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Abstract

Plasma cell leukemia (PCL) is an aggressive variant of multiple myeloma and is characterized by the presence of >20% and/or an absolute number of greater 2 × 10(9)/L plasma cells circulating in the peripheral blood. PCL represents approximately 2–4% of all MM diagnosis and exists in two forms: primary PCL (PPCL, 60% of cases) presents de novo, whereas secondary PCL (SPCL, accounts for the remaining 40%) consists of a leukemic transformation in patients with a previously diagnosed MM. Because the mechanisms contributing to the pathogenesis of PCL are not fully understood, immunophenotyping, genetic evaluation (conventional karyotype, FISH, GEP and array-CGH), and immunohistochemistry are really important tools to investigate why plasma cells escape from bone marrow and become highly aggressive. Since treatment with standard agents and steroids is poorly effective, a combination of new drugs as part of the induction regimens and bone marrow transplant (autologous and allogeneic approaches) could nearly overcome the poor prognosis exhibited by PCL patients.
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Metadata
Title
Plasma cell leukemia: a highly aggressive monoclonal gammopathy with a very poor prognosis
Authors
Victor H. Jimenez-Zepeda
Virginia J. Dominguez-Martinez
Publication date
01-04-2009
Publisher
Springer Japan
Published in
International Journal of Hematology / Issue 3/2009
Print ISSN: 0925-5710
Electronic ISSN: 1865-3774
DOI
https://doi.org/10.1007/s12185-009-0288-3

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