Li Elizabeth Huai-Feng, Davila Claire, Zuraski Connor, Chang Jennifer, Goodwill Vanessa, Farid Nikdokht
School of Medicine, UC San Diego, San Diego, CA, United States.
Department of Neurology, UC San Diego, San Diego, CA, United States.
Front Radiol. 2024 Nov 25;4:1479282. doi: 10.3389/fradi.2024.1479282. eCollection 2024.
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.
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.
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.
脑淋巴瘤病(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,非典型淋巴细胞弥漫性浸润脑实质,不像PCNSL那样形成离散的肿块。我们报告一例66岁女性,患有弥漫性CL并伴有PCNSL区域。她表现为亚急性认知功能减退和虚弱。脑脊液检查显示淋巴细胞增多和白细胞介素-10升高。尽管进行了类固醇和静脉注射免疫球蛋白试验,她仍变得越来越嗜睡,并在症状出现四个月后死于该病。
她最初的头部非增强CT显示脑室周围和皮质下白质、双侧基底神经节及脑桥中部有边界不清的低密度影,在脑部MRI上对应为弥漫性T2/液体衰减反转恢复序列(FLAIR)高信号。最初未发现异常强化、弥散受限或离散肿块。随后,磁共振波谱显示胆碱:肌酸异常升高,N-乙酰天门冬氨酸(NAA)峰降低,提示细胞增多过程。一个月后,MRI显示右侧尾状核和左侧海马区T2/FLAIR高信号越来越融合,伴有新的弥散受限,以及右侧尾状核新的高灌注。同样,这些区域未发现肿块或强化。尸检时,实质病理大多与CL一致。然而,右侧尾状核和左侧海马区有两个明确的PCNSL区域,尽管缺乏PCNSL的典型放射学特征,但与她最后一次MRI上新出现的异常区域相对应。
这是一例独特的CL合并PCNSL区域的病例。尽管CL被认为是PCNSL的一种独特亚型,但我们的病例表明PCNSL可能在弥漫性CL的背景下发生。对于有亚急性神经功能减退且MRI表现为弥漫性白质脑病的患者,应考虑弥漫性CL。