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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

机译: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集中于II型肠病相关的T细胞淋巴瘤和原发性肠道NK细胞淋巴瘤

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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.
机译:在中国是乳糜泻的非流行地区,原发性肠道T细胞和NK细胞淋巴瘤可能包含异质亚型。在中国很少报道II型肠病相关的T细胞淋巴瘤和原发性肠道NK细胞淋巴瘤。在这项研究中,我们检查了中国患者38例原发性肠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细胞受体基因重排分析的结果,NK细胞组中的所有肿瘤在大多数肿瘤细胞中均由爱泼斯坦-巴尔病毒编码的mRNA呈阳性,并且是多克隆的。 NK细胞组的存活率显着低于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个被认为是周围T细胞淋巴瘤,未另作说明(NOS)。在II型肠病相关的T细胞淋巴瘤组中,平均年龄为55岁。所有七名患者的II型与肠病相关的T细胞淋巴瘤肿瘤细胞均为单形,中等大小。 II型与肠病相关的T细胞淋巴瘤组的存活率显着低于外周T细胞淋巴瘤NOS组(P = 0.0181)。多变量分析表明,在我们的一系列原发性肠T细胞和NK细胞淋巴瘤患者中,NK细胞表型,男性性别和CD8阳性是不良预后的因素。综上所述,我国大多数原发性肠T细胞和NK细胞淋巴瘤病例均与乳糜泻无关,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。每个组具有独特的组织病理学特征,并具有预后意义。

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