Primary gastric EBV-positive cytotoxic-molecule-negative T-cell lymphoma with TET2 multihit mutations: a case report.

IF 1.4
Masako Kurashige, Akihisa Hino, Koki Muto, Keisuke Nagahama, Takehiro Yamamoto, Keiichi Nakata, Michiko Ichii, Kentaro Fukushima, Kennosuke Karube, Yasuhito Nannya, Naoki Hosen, Seishi Ogawa, Eiichi Morii
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Abstract

Extranodal NK/T-cell lymphoma (ENKTL) is an Epstein-Barr virus (EBV)-positive lymphoma of the NK- or cytotoxic T-cell lineage. According to the World Health Organization Classification of Hematolymphoid Tumors, Fifth Edition (WHO-HAEM5), EBV-positive cases lacking cytotoxic molecules cannot be classified as ENKTL. To the best of our knowledge, this is the first documented case of primary gastric EBV-positive T-cell lymphoma lacking the expression of cytotoxic molecules. A 76-year-old woman initially presented with a disease confined to the stomach, with subsequent contiguous extension into the duodenum. Biopsies revealed small- to medium-sized atypical T cells with pale cytoplasm and irregularly folded nuclei, as well as intravascular infiltration. Tumor cells were positive for CD3, TCRβF1, and CD4 and negative for CD56, TIA-1, granzyme B, perforin, and PD-L1. EBV-encoded RNA in situ hybridization highlighted neoplastic T cells. These findings did not fulfill the criteria for any T/NK cell entity of WHO-HAEM5 including ENKTL and peripheral T-cell lymphoma not otherwise specified (PTCL, NOS). Targeted sequencing revealed TET2 multihit mutations, suggesting clonal hematopoiesis-linked pathogenesis. Given the patient's age and tumor location, we administered a reduced dose of DeVIC, followed by radiotherapy, achieving partial remission. This case expands the spectrum of EBV-associated T-cell lymphomas and highlights the need for additional cases to refine the classification and management.

原发性胃ebv阳性细胞毒-分子阴性t细胞淋巴瘤伴TET2多击突变1例。
结外NK/ t细胞淋巴瘤(ENKTL)是一种eb病毒(EBV)阳性的NK或细胞毒性t细胞谱系淋巴瘤。根据世界卫生组织《血淋巴类肿瘤分类》第五版(WHO-HAEM5),缺乏细胞毒性分子的ebv阳性病例不能归类为ENKTL。据我们所知,这是第一例记录的原发性胃ebv阳性t细胞淋巴瘤缺乏细胞毒性分子的表达。一名76岁女性,最初表现为局限于胃的疾病,随后连续扩展到十二指肠。活检显示小到中型的非典型T细胞,胞质苍白,细胞核不规则折叠,并有血管内浸润。肿瘤细胞CD3、TCRβF1和CD4呈阳性,CD56、TIA-1、颗粒酶B、穿孔素和PD-L1呈阴性。ebv编码RNA原位杂交突出肿瘤T细胞。这些发现不符合WHO-HAEM5的任何T/NK细胞实体的标准,包括ENKTL和其他未指定的外周T细胞淋巴瘤(PTCL, NOS)。靶向测序显示TET2多命中突变,提示克隆造血相关发病机制。考虑到患者的年龄和肿瘤位置,我们使用了减少剂量的DeVIC,然后进行放疗,达到部分缓解。该病例扩大了ebv相关t细胞淋巴瘤的范围,并强调需要更多病例来完善分类和管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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