CD5/Cyclin D1双阴性多形性套细胞淋巴瘤的鉴定

W. Chuang, Sheng-Tsung Chang, Chang-Tsu Yuan, G. Chang, Hung Chang, Chi‐Ju Yeh, S. Ueng, Hsiao-Wen Kao, Tong-Hong Wang, Y. Wan, L. Shih, S. Chuang, C. Hsueh
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引用次数: 4

摘要

多形性套细胞淋巴瘤(PMCL)在形态学上与弥漫性大b细胞淋巴瘤(DLBCL)相似,CD5和cyclin D1的表达有助于鉴别诊断。迄今为止,没有CD5/cyclin D1双阴性PMCL病例的报道。包括4例免疫表型为CD5(−)cyclin D1(−)SOX11(+)的b细胞淋巴瘤,形态学特征与DLBCL相容。其中2例是先前发现的,另外2例是从500例b细胞淋巴瘤中筛选出来的。我们分析了他们的临床病理、免疫表型、遗传和基因表达特征。并对cyclin d1阳性PMCL、cyclin d1阴性PMCL、生发中心B细胞(GCB) DLBCL、活化B细胞(ABC) DLBCL进行比较。与其他PMCL病例相似,这4例患者以老年男性为主,临床病程具有侵袭性。这些肿瘤均未检测到涉及CCND1、CCND2、CCND3、CCNE1、CCNE2、MYC、BCL2或BCL6的易位。这4例病例的全基因组拷贝数谱与cyclin d1阴性PMCL相似。这些肿瘤中没有cyclin D1、cyclin D2或cyclin D3的高表达。与cyclin d1阴性PMCL类似,与cyclin d1阳性PMCL相比,这些病例的cyclin E1和cyclin E2表达更高。这些肿瘤的基因表达模式也与cyclin d1阴性PMCL相似。本文首次报道4例CD5/cyclin D1双阴性PMCL。SOX11阳性有助于鉴别这些罕见肿瘤,进一步的遗传和基因表达分析可用于确诊。
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Identification of CD5/Cyclin D1 Double-negative Pleomorphic Mantle Cell Lymphoma
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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