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Isolated lymphomatoid granulomatosis of the central nervous system: A case report and literature review

机译:中枢神经系统分离的淋巴瘤肉芽肿症:案例报告与文献综述

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摘要

Lymphomatoid granulomatosis (LYG) is an angiocentric and angiodestructive lymphoproliferative disease which can involve multiple organs of the body and is most common in the lungs. Its pathological features are proliferation of large atypical B‐cells related to Epstein–Barr virus, T‐cell infiltration and tissue necrosis. This disease is rare, and LYG which uniquely involves the central nervous system (CNS) is extremely rare. In this paper, we report a case of isolated lymphomatoid granulomatosis of the CNS (iCNS‐LYG) diagnosed by histological biopsy and we review the clinical features of all similar cases reported in the past 46?years. A total of 49 cases of iCNS‐LYG have been reported to date. The clinical, imaging and pathological features of iCNS‐LYG are discussed in combination with a literature review.
机译:淋巴瘤肉芽肿病(LYG)是一种血管监管和血管病性淋巴抑制性疾病,可涉及身体的多个器官,并且在肺中最常见。 其病理特征是与Epstein-Barr病毒,T细胞浸润和组织坏死相关的大型非典型B细胞的增殖。 这种疾病是罕见的,并且唯一涉及中枢神经系统(CNS)的LYG非常罕见。 在本文中,我们报告了组织学活组织检查诊断的CNS(ICNS-LYG)的分离淋巴瘤颗粒状芽孢杆菌病例,并审查了过去46年过去报道的所有类似病例的临床特征。 迄今已举报共49例ICNS-LYG。 ICNS-LYG的临床,成像和病理特征与文献综述结合讨论。

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