Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Mod Pathol. 2011 Jul;24(7):983-92. doi: 10.1038/modpathol.2011.45. Epub 2011 Mar 18.
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.
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。