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Nasal natural killer (NK)/T-cell lymphoma: clinical, histological, virological, and genetic features

机译:鼻自然杀伤(NK)/ T细胞淋巴瘤:临床,组织学,病毒学和遗传学特征

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Nasal natural killer (NK)/T-cell lymphoma (NNKTL) is a clinical illness characterized by progressive unrelenting ulceration and necrosis of the nasal cavity and midline facial tissues. Histological features of the lymphoma include angiocentric and polymorphous lymphoreticular infiltrates, called polymorphic reticulosis. Surface antigens and the NK-cell marker, CD56, as well as pan-T antigen CD2, cytoplasmic CD3 (CD3?), and CD45 are expressed in the lymphoma cells. The origin of the lymphoma is thought to be either NK-cell linkage without T-cell receptor (TCR) rearrangement or γδT-cell linkage with γδTCR rearrangement. Since the authors of this study first demonstrated the presence of Epstein Barr virus (EBV)-DNA and EBV oncogenic proteins in NNKTL, the lymphoma has been classified as one of the EBV-associated malignancies. The NNKTL cells produce interleukin (IL)-9, IL-10, and interferon-γ-inducible protein-10 (IP-10), possibly due to EBV-oncogenic proteins in the lymphoma cells, and such cytokines take an important part in the cell proliferation and invasion, acting in an autocrine manner. Clinically, the serum EBV-DNA copy number is useful as a specific tumor marker and a predictive prognostic factor. Even in early clinical stages, the lymphoma shows poor prognosis caused by the rapid progression of the lesion into distinct organs. Our newly designed arterial infusion chemotherapy, from the superficial temporal artery, in combination with radiotherapy, has shown a favorable outcome in patients with NNKTL. In this article, the clinical, pathological, and virological characteristics of the lymphoma are reviewed, along with a report of our investigations.
机译:鼻自然杀手(NK)/ T细胞淋巴瘤(NNKTL)是一种临床疾病,其特征是鼻腔和中线面部组织进行性持续性溃疡和坏死。淋巴瘤的组织学特征包括血管中心性和多形性淋巴网状浸润,称为多形性网织病。表面抗原和NK细胞标志物CD56以及pan-T抗原CD2,细胞质CD3(CD3α)和CD45在淋巴瘤细胞中表达。淋巴瘤的起源被认为是没有T细胞受体(TCR)重排的NK细胞连接或具有γδTCR重排的γδT细胞连接。自从这项研究的作者首次证明NNKTL中存在爱泼斯坦巴尔病毒(EBV)-DNA和EBV致癌蛋白以来,淋巴瘤已被归类为EBV相关的恶性肿瘤之一。 NNKTL细胞产生白介素(IL)-9,IL-10和干扰素-γ诱导型蛋白10(IP-10),这可能是由于淋巴瘤细胞中的EBV致癌蛋白所致,而这种细胞因子在细胞以自分泌方式发挥作用。临床上,血清EBV-DNA拷贝数可用作特定的肿瘤标志物和预测预后因素。即使在早期临床阶段,淋巴瘤也显示出由于病变迅速发展为不同器官而导致的预后不良。我们新设计的来自颞浅动脉的动脉灌注化疗,结合放疗,已在NNKTL患者中显示出良好的疗效。在本文中,对淋巴瘤的临床,病理和病毒学特征进行了综述,并提供了我们的研究报告。

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