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Tytuł pozycji:

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

Tytuł:
Identification of CD5/Cyclin D1 Double-negative Pleomorphic Mantle Cell Lymphoma: A Clinicopathologic, Genetic, and Gene Expression Study.
Autorzy:
Chuang WY; Department of Pathology.; Graduate Institute of Clinical Medical Sciences, College of Medicine.
Chang ST; Department of Pathology, Chi-Mei Medical Center.; Department of Nursing, National Tainan Institute of Nursing, Tainan.
Yuan CT; Department of Pathology, National Taiwan University Hospital, College of Medicine, National Taiwan University.
Chang GJ; Graduate Institute of Clinical Medical Sciences, College of Medicine.
Chang H; Department of Internal Medicine, Division of Hematology and Oncology.
Yeh CJ; Department of Pathology.
Ueng SH; Department of Pathology.
Kao HW; Department of Internal Medicine, Division of Hematology and Oncology.
Wang TH; Tissue Bank.
Wan YL; Department of Medical Imaging and Intervention, Chang Gung Memorial Hospital.
Shih LY; Department of Internal Medicine, Division of Hematology and Oncology.
Chuang SS; Department of Pathology, Chi-Mei Medical Center.; Department of Pathology, School of Medicine, Taipei Medical University and National Taiwan University, Taipei, Taiwan.
Hsueh C; Department of Pathology.; Tissue Bank.; Chang Gung Molecular Medicine Research Center, Chang Gung University, Taoyuan.
Źródło:
The American journal of surgical pathology [Am J Surg Pathol] 2020 Feb; Vol. 44 (2), pp. 232-240.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Publication: <2015- > : Philadelphia, PA : Wolters Kluwer Health, Inc.
Original Publication: New York, Masson.
MeSH Terms:
Gene Expression Regulation, Neoplastic*
Biomarkers, Tumor/*metabolism
CD5 Antigens/*metabolism
Cyclin D1/*metabolism
Lymphoma, Large B-Cell, Diffuse/*diagnosis
Lymphoma, Mantle-Cell/*diagnosis
SOXC Transcription Factors/*metabolism
Adult ; Aged ; Aged, 80 and over ; Biomarkers, Tumor/genetics ; CD5 Antigens/genetics ; Cyclin D1/genetics ; Diagnosis, Differential ; Gene Expression Profiling ; Humans ; Immunohistochemistry ; In Situ Hybridization, Fluorescence ; Lymphoma, Large B-Cell, Diffuse/genetics ; Lymphoma, Large B-Cell, Diffuse/pathology ; Lymphoma, Mantle-Cell/genetics ; Lymphoma, Mantle-Cell/pathology ; Male ; Middle Aged ; Phenotype ; SOXC Transcription Factors/genetics
References:
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Liu Z, Dong HY, Gorczyca W, et al. CD5− mantle cell lymphoma. Am J Clin Pathol. 2002;118:216–224.
Chuang WY, Chang H, Chang GJ, et al. Pleomorphic mantle cell lymphoma morphologically mimicking diffuse large B cell lymphoma: common cyclin D1 negativity and a simple immunohistochemical algorithm to avoid the diagnostic pitfall. Histopathology. 2017;70:986–999.
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Substance Nomenclature:
0 (Biomarkers, Tumor)
0 (CCND1 protein, human)
0 (CD5 Antigens)
0 (SOX11 protein, human)
0 (SOXC Transcription Factors)
136601-57-5 (Cyclin D1)
Entry Date(s):
Date Created: 20191106 Date Completed: 20200513 Latest Revision: 20210131
Update Code:
20240104
DOI:
10.1097/PAS.0000000000001390
PMID:
31688139
Czasopismo naukowe
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.

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