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一例自然杀伤/T细胞谱系EB病毒阴性原发性中枢神经系统淋巴瘤的罕见病例。

An Unusual Case of EBV-Negative Primary CNS Lymphoma of Natural Killer/T-Cell Lineage.

作者信息

Kajtazi Naim I, Bafaquh Mohammed, Ghamdi Juman Al, AlEissa Zahra, Shmeikh Arwa Al, Alsaeed Ali, Sulaiman Tarek, Vizcaino M Adelita, Al Hameed Majed, Raghunathan Aditya

机构信息

Department of Neurology, National Neurosciences Institute, King Fahad Medical City, Riyadh, KSA.

Department of Neurosurgery, National Neurosciences Institute, King Fahad Medical City, Riyadh, KSA.

出版信息

Clin Pathol. 2021 Dec 12;14:2632010X211065692. doi: 10.1177/2632010X211065692. eCollection 2021 Jan-Dec.

Abstract

Extranodal NK/T-cell lymphoma (ENKTL) is a well-defined cytotoxic lymphoma strongly associated with Epstein-Barr virus (EBV) infection, commonly affecting the nasopharynx and upper aerodigestive tract. Primary central nervous system (CNS) involvement is rare, and only 17 cases were previously reported in the literature. Here, we report the case of a 44-year-old male admitted with a 3-month history of personality changes and progressive right leg weakness. Brain magnetic resonance imaging studies (MRIs) revealed multiple rim-enhancing brain lesions bilaterally. An extensive clinical and laboratory workup was unrevealing, and 2 brain biopsies were initially considered inconclusive. Pertinently, no systemic lymphoproliferative disorder was identified. The patient initially experienced remarkable clinical improvement with dexamethasone, pulse methylprednisolone, and rituximab therapy. However, he eventually had rapid clinical deterioration, was found to have increased brain lesions, and died nearly 6 months after the initial presentation. During this time, the second brain biopsy was found to show involvement by T-cell lymphoma of NK-cell lineage, which was EBV negative. No post-mortem examination was done to identify any systemic lymphoma. This case serves to expand the spectrum of lymphomas involving the CNS.

摘要

结外NK/T细胞淋巴瘤(ENKTL)是一种明确的细胞毒性淋巴瘤,与爱泼斯坦-巴尔病毒(EBV)感染密切相关,常见于鼻咽部和上呼吸消化道。原发性中枢神经系统(CNS)受累罕见,此前文献仅报道过17例。在此,我们报告一例44岁男性患者,因3个月的人格改变和进行性右腿无力入院。脑部磁共振成像(MRI)研究显示双侧多个环形强化脑病变。广泛的临床和实验室检查未发现异常,最初的2次脑活检结果不明确。相关的是,未发现系统性淋巴增殖性疾病。患者最初接受地塞米松、甲泼尼龙冲击治疗和利妥昔单抗治疗后临床有显著改善。然而,他最终临床迅速恶化,发现脑病变增多,在首次就诊近6个月后死亡。在此期间,第二次脑活检显示为NK细胞系T细胞淋巴瘤受累,EBV阴性。未进行尸检以确定是否存在系统性淋巴瘤。该病例有助于扩大累及中枢神经系统的淋巴瘤谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/8671822/a9f14678a6d7/10.1177_2632010X211065692-fig1.jpg

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