Case Report: Diffuse cerebral lymphomatosis with superimposed multifocal primary CNS lymphoma.

Frontiers in radiology Pub Date : 2024-11-25 eCollection Date: 2024-01-01 DOI:10.3389/fradi.2024.1479282
Elizabeth Huai-Feng Li, Claire Davila, Connor Zuraski, Jennifer Chang, Vanessa Goodwill, Nikdokht Farid
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Abstract

Description: Cerebral lymphomatosis (CL) is a rare subtype of primary central nervous system lymphoma (PCNSL). In CL, atypical lymphoid cells diffusely infiltrate the cerebral parenchyma without forming a discrete mass as seen with PCNSL. We report a case of a 66-year-old woman with diffuse CL and superimposed areas of PCNSL. She presented with subacute cognitive decline and weakness. CSF studies showed lymphocytosis and IL-10 elevation. She became increasingly somnolent despite steroid and intravenous immunoglobulin trials, and she succumbed to the disease four months after symptom onset.

Radiologic findings: Her initial non-contrast head CT showed ill-defined hypodensities in the periventricular and subcortical white matter, bilateral basal ganglia, and central pons, which corresponded to diffuse T2/FLAIR hyperintensities on brain MRI. No abnormal enhancement, diffusion restriction, or discrete mass was present initially. Subsequently, MR spectroscopy demonstrated abnormally elevated choline:creatine and decreased NAA peaks, suggesting a hypercellular process. One month later, MRI revealed increasingly confluent T2/FLAIR hyperintensities with new diffusion restriction in the right caudate and left hippocampus, as well as new hyperperfusion in the right caudate. Again, no mass or enhancement was identified in these areas. On autopsy, parenchymal pathology was mostly consistent with CL. However, there were two areas of frank PCNSL in the right caudate and left hippocampus, which corresponded to the new areas of abnormality on her last MRI despite lacking the typical radiologic features of PCNSL.

Novel aspects: This is a unique case of CL with concurrent areas of PCNSL. Although CL is thought to be a distinct subtype of PCNSL, our case demonstrates that PCNSL may develop on a background of diffuse CL. In patients with subacute neurologic decline and MRI findings of diffuse leukoencephalopathy, diffuse CL should be considered.

病例报告:弥漫性脑淋巴瘤合并原发性多灶性中枢神经系统淋巴瘤。
描述:脑淋巴瘤(CL)是原发性中枢神经系统淋巴瘤(PCNSL)的一种罕见亚型。在CL中,不典型淋巴样细胞弥漫性浸润脑实质,而不形成PCNSL所见的离散肿块。我们报告一例66岁女性弥漫性CL和PCNSL重叠区域。她表现出亚急性认知能力下降和虚弱。脑脊液检查显示淋巴细胞增多和IL-10升高。尽管进行了类固醇和静脉注射免疫球蛋白的试验,她还是变得越来越嗜睡,在症状出现四个月后,她死于这种疾病。影像学表现:患者最初的非对比头部CT显示脑室周围和皮层下白质、双侧基底节区和脑桥中央密度低,与脑部MRI上弥漫性T2/FLAIR高信号一致。最初没有异常增强、扩散限制或离散质量。随后,磁共振光谱显示异常升高的胆碱和肌酸和降低的NAA峰,提示高细胞过程。1个月后,MRI显示T2/FLAIR高信号逐渐融合,右侧尾状和左侧海马出现新的扩散限制,右侧尾状出现新的高灌注。同样,在这些区域没有发现肿块或强化。尸检时,实质病理基本符合CL。然而,在右侧尾状核和左侧海马体中有两个明显的PCNSL区域,尽管缺乏典型的PCNSL放射学特征,但这与她最后一次MRI上的新异常区域相对应。新颖方面:这是一个独特的CL与PCNSL并发区域的案例。虽然CL被认为是PCNSL的一个不同亚型,但我们的病例表明PCNSL可能在弥漫性CL的背景下发展。在亚急性神经功能减退和MRI表现为弥漫性脑白质病的患者中,应考虑弥漫性CL。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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