Article

Clinical, immunophenotypic, and genetic characterization of small lymphocyte-like plasma cell myeloma: a potential mimic of mature B-cell lymphoma.

Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, USA.
American Journal of Clinical Pathology (impact factor: 2.6). 02/2010; 133(2):265-70. DOI:10.1309/AJCPUS3PRRT5ZXVS pp.265-70
Source: PubMed

ABSTRACT We reviewed bone marrow studies from 351 multiple myeloma (MM) cases, selecting 12 cases (3.4%) with predominantly small lymphocyte-like morphologic features resembling B-cell lymphoma, and correlated their genetic and clinical features. All exhibited a diffuse interstitial pattern of marrow involvement. Small lymphocyte-like plasma cells were all CD45- with bright CD38 and CD138 expression and CD20 expression in 5 cases. No case had an increase in bone marrow B lymphocytes by flow cytometry. Of 12 cases, 9 were classified as the CD-2 molecular class by gene expression profiling (GEP). The 29 CD-2 class cases with (n = 9) and without (n = 20) small lymphocyte-like features could not be discerned from one another using global GEP. Event-free, but not overall, survival was significantly better in cases with small lymphocyte-like features among those sharing the CD-2 subtype. Small lymphocyte-like MM is a rare, morphologically challenging variant distinguished from B-cell lymphoma by lack of CD45 and presence of CD138 and the clinical presentation of MM. Most cases share a common GEP signature dominated by hyperexpression of cyclin D1 or cyclin D3 genes, with increased expression of the B-cell genes CD20 and VPREB3.

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Keywords

29 CD-2 class cases
 
5 cases
 
B-cell genes CD20
 
bone marrow B lymphocytes
 
bone marrow studies
 
bright CD38
 
cases share
 
CD-2 molecular class
 
CD138 expression
 
CD20 expression
 
clinical features
 
common GEP signature
 
cyclin D3 genes
 
diffuse interstitial pattern
 
gene expression profiling
 
hyperexpression
 
small lymphocyte-like features
 
small lymphocyte-like morphologic features
 
Small lymphocyte-like plasma cells
 
using global GEP