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  4. Identification of CD5/Cyclin D1 Double-negative Pleomorphic Mantle Cell Lymphoma: A Clinicopathologic, Genetic, and Gene Expression Study
 
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Identification of CD5/Cyclin D1 Double-negative Pleomorphic Mantle Cell Lymphoma: A Clinicopathologic, Genetic, and Gene Expression Study

Journal
American Journal of Surgical Pathology
Journal Volume
44
Journal Issue
2
Pages
232-240
Date Issued
2020
Author(s)
Chuang W.-Y.
Chang S.-T.
CHANG-TSU YUAN  
Chang G.-J.
Chang H.
Yeh C.-J.
Ueng S.-H.
Kao H.-W.
Wang T.-H.
Wan Y.-L.
Shih L.-Y.
Chuang S.-S.
Hsueh C.
DOI
10.1097/PAS.0000000000001390
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85074556868&doi=10.1097%2fPAS.0000000000001390&partnerID=40&md5=87f015491d9b5ccfcbf77bbeb8824e63
https://scholars.lib.ntu.edu.tw/handle/123456789/585851
Abstract
Pleomorphic mantle cell lymphoma (PMCL) can closely mimic diffuse large B-cell lymphoma (DLBCL) morphologically, and expression of CD5 and cyclin D1 is helpful for differential diagnosis. To date, no cases of CD5/cyclin D1 double-negative PMCL have been reported. Four cases of B-cell lymphoma with an immunophenotype of CD5(-) cyclin D1(-) SOX11(+) and morphologic features compatible with DLBCL were included. Two were previously identified, and the other 2 were screened from 500 cases of B-cell lymphoma. We analyzed their clinicopathologic, immunophenotypic, genetic, and gene expression features. Cases of cyclin D1-positive PMCL, cyclin D1-negative PMCL, germinal center B-cell (GCB) DLBCL, and activated B cell (ABC) DLBCL were also studied for comparison. Similar to other PMCL cases, these 4 patients were mainly elderly male individuals with an aggressive clinical course. None of these tumors had detectable translocations involving CCND1, CCND2, CCND3, CCNE1, CCNE2, MYC, BCL2, or BCL6. The genome-wide copy number profile of these 4 cases was similar to that of cyclin D1-negative PMCL. None of these tumors had high expression of cyclin D1, cyclin D2, or cyclin D3. Similar to cyclin D1-negative PMCL, these cases had higher expression of cyclin E1 and cyclin E2 compared with cyclin D1-positive PMCL. The gene expression pattern of these tumors was also similar to that of cyclin D1-negative PMCL. Here we report for the first time 4 cases of CD5/cyclin D1 double-negative PMCL. SOX11 positivity is useful to identify these rare tumors, and further genetic and gene expression analysis can be used to confirm the diagnosis.
SDGs

[SDGs]SDG3

Publisher
Lippincott Williams and Wilkins
Type
journal article

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