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皮下脂膜炎样 T 细胞淋巴瘤、深部狼疮和重叠病例:通过研究 208 个基因进行分子特征分析。

Subcutaneous panniculitis-like T-cell lymphoma, lupus erythematosus profundus, and overlapping cases: molecular characterization through the study of 208 genes.

机构信息

Department of Dermatology, Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Madrid, Spain.

Department of Pathology, Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Madrid, Spain.

出版信息

Leuk Lymphoma. 2021 Sep;62(9):2130-2140. doi: 10.1080/10428194.2021.1901098. Epub 2021 May 8.

DOI:10.1080/10428194.2021.1901098
PMID:33966586
Abstract

Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare cytotoxic cutaneous lymphoma. Differential diagnosis with lupus erythematosus panniculitis (LEP) can be challenging and overlapping cases have been described. In this study, we investigate whether gene expression profiling may or not identify markers that can be used to improve our understanding of the disease and to make a precise differential diagnosis. SPTCL, LEP, and overlapping cases were analyzed using a customized NanoString platform including 208 genes related to T-cell differentiation, stromal signatures, oncogenes, and tumor suppressor genes. Gene expression unsupervised analysis of the samples differentiated SPTCL from LEP samples. Most overlapping cases were clustered with LEP cases. Differentially expressed genes were observed when comparing SPTCL with LEP cases; and overlapping with LEP cases. Gene set enrichment analysis recognized gene sets defining each group. In conclusion, SPTCL and LEP have distinctive molecular profiles and the molecular background of overlapping cases more closely resembles LEP.

摘要

皮下脂膜炎样 T 细胞淋巴瘤(SPTCL)是一种罕见的细胞毒性皮肤淋巴瘤。与狼疮性脂膜炎(LEP)的鉴别诊断具有挑战性,已有重叠病例的描述。在这项研究中,我们研究了基因表达谱是否可以识别出可用于提高我们对疾病的认识并进行精确鉴别诊断的标志物。使用包括与 T 细胞分化、基质特征、癌基因和肿瘤抑制基因相关的 208 个基因的定制 NanoString 平台分析了 SPTCL、LEP 和重叠病例。对样本的无监督基因表达分析将 SPTCL 与 LEP 样本区分开来。大多数重叠病例与 LEP 病例聚类。比较 SPTCL 与 LEP 病例时观察到差异表达基因;并与 LEP 病例重叠。基因集富集分析识别了定义每个组的基因集。总之,SPTCL 和 LEP 具有独特的分子特征,重叠病例的分子背景更类似于 LEP。

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引用本文的文献

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