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原发性肠道 T 细胞和 NK 细胞淋巴瘤:来自中国的临床病理和分子研究,重点关注 II 型肠病相关 T 细胞淋巴瘤和原发性肠道 NK 细胞淋巴瘤。

Primary intestinal T-cell and NK-cell lymphomas: a clinicopathological and molecular study from China focused on type II enteropathy-associated T-cell lymphoma and primary intestinal NK-cell lymphoma.

机构信息

Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.

出版信息

Mod Pathol. 2011 Jul;24(7):983-92. doi: 10.1038/modpathol.2011.45. Epub 2011 Mar 18.

Abstract

In China, which is a non-endemic area for celiac disease, primary intestinal T-cell and NK-cell lymphomas might comprise heterogeneous subtypes. Both type II enteropathy-associated T-cell lymphoma and primary intestinal NK-cell lymphoma are rarely reported and poorly characterized in China. In this study, we examined the clinicopathological and molecular features of 38 cases of primary intestinal T-cell and NK-cell lymphoma in Chinese patients. Based on these findings, we first classified the patients into an NK-cell group (n=6) and a T-cell group (n=32). In the NK-cell group, the mean age was 37 years. All tumors of the NK-cell group were positive for Epstein-Barr virus encoded mRNA in the majority of tumor cells and were polyclonal according to the results of commercial BIOMED-2 T-cell receptor gene rearrangement assays. The survival in the NK-cell group was significantly worse than that of the T-cell group (P=0.0247). Next, 7 tumors of the T-cell group were considered type II enteropathy-associated T-cell lymphoma, while 24 were considered peripheral T-cell lymphoma, not otherwise specified (NOS). In the type II enteropathy-associated T-cell lymphoma group, the mean age was 55 years. Type II enteropathy-associated T-cell lymphoma tumor cells from all seven patients were monomorphic, medium sized. The survival in the type II enteropathy-associated T-cell lymphoma group was significantly worse than that of the peripheral T-cell lymphoma, NOS group (P=0.0181). Multivariate analysis identified NK-cell phenotype, male gender, and CD8 positivity as factors for poor prognosis in our series of primary intestinal T-cell and NK-cell lymphoma patients. In conclusion, most cases of primary intestinal T-cell and NK-cell lymphoma in China are not associated with celiac disease and could be classified to NK-cell group, type II enteropathy-associated T-cell lymphoma group, and peripheral T-cell lymphoma, NOS group. Each group has distinctive histopathological features with prognostic significance.

摘要

在中国,原发性肠道 T 细胞和 NK 细胞淋巴瘤是非麸质疾病的地方性疾病,可能包含异质性亚型。II 型肠病相关 T 细胞淋巴瘤和原发性肠道 NK 细胞淋巴瘤在中国很少报道,特征描述也很差。在这项研究中,我们检查了 38 例中国患者原发性肠道 T 细胞和 NK 细胞淋巴瘤的临床病理和分子特征。基于这些发现,我们首先将患者分为 NK 细胞组(n=6)和 T 细胞组(n=32)。在 NK 细胞组中,平均年龄为 37 岁。根据商业 BIOMED-2 T 细胞受体基因重排检测结果,NK 细胞组的所有肿瘤均为多数肿瘤细胞中 EBV 编码 mRNA 阳性,呈多克隆性。NK 细胞组的生存显著差于 T 细胞组(P=0.0247)。接下来,T 细胞组的 7 个肿瘤被认为是 II 型肠病相关 T 细胞淋巴瘤,而 24 个被认为是外周 T 细胞淋巴瘤,非特指型(NOS)。在 II 型肠病相关 T 细胞淋巴瘤组中,平均年龄为 55 岁。来自所有 7 名患者的 II 型肠病相关 T 细胞淋巴瘤肿瘤细胞均为单形性、中等大小。II 型肠病相关 T 细胞淋巴瘤组的生存显著差于外周 T 细胞淋巴瘤,NOS 组(P=0.0181)。多变量分析确定 NK 细胞表型、男性和 CD8 阳性是本系列原发性肠道 T 细胞和 NK 细胞淋巴瘤患者预后不良的因素。总之,中国大多数原发性肠道 T 细胞和 NK 细胞淋巴瘤与乳糜泻无关,可分为 NK 细胞组、II 型肠病相关 T 细胞淋巴瘤组和外周 T 细胞淋巴瘤,NOS 组。每个组都具有独特的组织病理学特征和预后意义。

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