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A clinical research on imaging and pathological features of primary central nervous system lymphoma

机译:原发性中枢神经系统淋巴瘤的影像学和病理学特征的临床研究

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Objective To investigate the clinical features, imaging and pathological characteristics of primary central nervous system lymphoma (PCNSL) in order to increase the diagnostic accuracy of PCNSL in clinic. Methods A retrospective analysis of 6 cases with PCNSL confirmed by pathological and immunohistochemical examination, treated in our hospital from December 2013 to August 2014 was performed. The clinical presentations, lesion locations, imaging manifestations and histopathological features were analysed. Results The symptoms were various, among which headache and dizziness were frequently presented. Five cases were identified to have solitary tumor foci and the other one had multiple lesions. Among 7 lesions, 4 were located in cerebral hemisphere, one was located in cerebellum, one in lateral ventricle and one in thalamus. Moreover, 2 lesions were involved in corpus callosum. The lesions presented in roundish shape or irregular shape with clear boundary, minimal edema and mass effect. CT showed high-density of the lesions. All lesions showed iso- or slightly hypo-intense signal on T1WI and iso- or mild hyper-intense on T2WI, and homogeneous enhancement after contrast. All cases underwent operations. The tumors appeared flesh red or grey-white, soft and without capsules. Under microscopic examination, the tumor cells were distributed around the blood vessels as "sleeve-like" infiltration. Immune phenotype analysis showed all tumors were B-cell lymphoma. Conclusions PCNSL has certain imaging and pathological features and most of them are diffuse large B-cell lymphoma (DLBCL). Pathological?examination and immune phenotype analysis are "gold standard" in making confirmed diagnosis.?DOI: 10.3969/j.issn.1672-6731.2016.11.014.
机译:目的探讨原发性中枢神经系统淋巴瘤(PCNSL)的临床特征,影像学和病理学特征,以提高PCNSL在临床上的诊断准确性。方法回顾性分析我院2013年12月至2014年8月收治的6例经病理和免疫组化确诊的PCNSL患者的临床资料。分析了临床表现,病变部位,影像学表现和组织病理学特征。结果症状多种多样,其中以头痛,头晕多见。确定了5例具有孤立肿瘤灶的病例,另一例有多个病灶。在7个病变中,有4个位于大脑半球,一个位于小脑,一个位于侧脑室,一个位于丘脑。此外,2体累及2个病变。病灶呈圆形或不规则形,边界清晰,水肿小,肿块少。 CT显示病变高密度。所有病变在T1WI上显示等强度或低强度信号,在T2WI上显示等强度或轻度高强度信号,对比后均增强。所有案件都进行了手术。肿瘤呈肉红色或灰白色,软且无包膜。在显微镜检查下,肿瘤细胞以“套管样”浸润的形式分布在血管周围。免疫表型分析显示所有肿瘤均为B细胞淋巴瘤。结论PCNSL具有一定的影像学和病理学特征,多数为弥漫性大B细胞淋巴瘤(DLBCL)。病理检查和免疫表型分析是确定诊断的“金标准”。DOI:10.3969 / j.issn.1672-6731.2016.11.014。

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