Findings at presentation in primary CNS diffuse large B-cell lymphoma of the brain: A comparison of immunocompetent and immunodeficient patients

C. Sampedro, Juan D. Corroto, M. Arias, J. C. Murua, M. F. Fontanillo, A. Castañón, J. P. Cebreiro
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引用次数: 2

Abstract

Background/Objectives: Primary central nervous system lymphoma (PCNSL) is a rare tumour with poor prognosis. Due to the increased number of patients with PCNSL over the past two decades our purpose are to describe magnetic resonance imaging (MRI) and Computed Tomography (CT) findings in (PCNSL) of the brain, and to study the differences between immunocompetent and immunodeficient patients with PCNSL. Methods : A retrospective, descriptive study was performed with 59 patients diagnosed of PCNSL in two hospitals from 1997 to 2010. Immunocompetent (n=38) and immunodeficient (n=21) patients were compared and differences between both groups were analyzed. Patients were evaluated according to sex, age, median time from clinical symptoms presentation to pathologic diagnosis, clinical symptoms, location, number of lesions, size, MRI and CT characteristics. Significance was defined as p < 0.05. Results : MRI findings: 50% of lesions in immunocompetent and 52.4% in immunodeficient group were heterogeneous, 89.5% of lesions in immunocompetent and 85,7% in immunodeficient were hypo-isointense on T1WI; 63.2% of lesions in immunocompetent and 76.2% in immunodeficient group were hyperintense on T2WI. CT images: 48.39% of lesions in immunocompetent and 20% in immunodeficient group were hyperdense. Statistically significant differences between immunocompetent and immunodeficient patients were found when evaluating the age ( p < 0.000) and median time from clinical symptoms presentation to pathologic diagnosis ( p < 0.008). Conclusions: MRI and CT are able to define imaging characteristics of PCNSL, promoting a quick diagnosis. There are no significant differences between immunocompetent and immunodeficient patients for MR and CT features.
原发性中枢神经系统弥漫性大b细胞淋巴瘤的表现:免疫正常和免疫缺陷患者的比较
背景/目的:原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的预后较差的肿瘤。由于过去二十年来PCNSL患者数量的增加,我们的目的是描述脑PCNSL的磁共振成像(MRI)和计算机断层扫描(CT)结果,并研究免疫功能正常和免疫缺陷的PCNSL患者之间的差异。方法:对1997 ~ 2010年在两所医院诊断为PCNSL的59例患者进行回顾性、描述性研究。比较免疫正常(n=38)和免疫缺陷(n=21)患者,分析两组差异。根据患者的性别、年龄、从临床症状出现到病理诊断的中位时间、临床症状、部位、病变数量、大小、MRI和CT特征进行评估。显著性定义为p < 0.05。结果:MRI表现:免疫正常组病变50%、免疫缺陷组病变52.4%呈异质性,免疫正常组病变89.5%、免疫缺陷组病变85.7%呈低等强度T1WI;免疫正常组和免疫缺陷组分别有63.2%和76.2%的病变呈T2WI高信号。CT表现:免疫正常组48.39%、免疫缺陷组20%病变呈高密度。免疫功能正常和免疫缺陷患者的年龄(p < 0.000)和从临床症状出现到病理诊断的中位时间(p < 0.008)差异有统计学意义。结论:MRI和CT能明确PCNSL的影像学特征,有助于快速诊断。免疫功能正常和免疫缺陷患者的MR和CT特征无显著差异。
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