Progressive Multifocal Leukoencephalopathy in a Patient With Cirrhosis and Hepatocellular Carcinoma.

IF 0.9 Q4 CLINICAL NEUROLOGY
Neurohospitalist Pub Date : 2024-10-01 Epub Date: 2024-06-03 DOI:10.1177/19418744241259072
Eric Caliendo, Sally Williams, Spencer Hutto, Annie Massart, Brianna Burlock, Brent Weinberg, Julien Cavanagh, Hang Shi
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引用次数: 0

Abstract

The following case describes a constellation of progressive cognitive and motor deficits in a 73-year-old man with cirrhosis and history of early-stage hepatocellular carcinoma confined to his liver. He had deficits in calculation, language, and writing, as well as subtle right-sided weakness. Magnetic resonance imaging (MRI) of the brain demonstrated non-enhancing white matter lesions without mass effect in the bilateral parietal and left occipitotemporal regions, correlating with neurologic exam findings. The patient's basic blood and cerebrospinal fluid (CSF) studies were within normal limits. Our differential included inflammatory and demyelinating conditions, hepatic encephalopathy, posterior reversible encephalopathy syndrome, progressive multifocal leukoencephalopathy (PML), and central nervous system (CNS) tumors. He did not improve with an empiric course of high-dose steroids or adequate hepatic encephalopathy treatment. A repeat lumbar puncture sent for additional CSF studies revealed a positive John Cunningham (JC) virus PCR test, confirming diagnosis of PML. Although the patient did not have any known overt immunosuppressive condition or treatment, the patient's cirrhosis and age placed him at higher risk for developing JC virus CNS reactivation. In a published case series of patients with PML and no classic immunosuppressive condition that includes several patients with concomitant cirrhosis, prognosis is much worse compared to those with known, reversible causes of immunosuppression.

肝硬化合并肝细胞癌患者的进行性多灶性白质脑病
以下病例描述的是一名 73 岁的男性,患有肝硬化和局限于肝脏的早期肝细胞癌,并逐渐出现认知和运动障碍。他在计算、语言和书写方面存在障碍,右侧肢体也有轻微无力。脑部磁共振成像(MRI)显示,双侧顶叶和左枕颞区的白质病变无增强,无肿块效应,与神经系统检查结果相关。患者的基本血液和脑脊液(CSF)检查均在正常范围内。我们的鉴别诊断包括炎症和脱髓鞘疾病、肝性脑病、后可逆性脑病综合征、进行性多灶性白质脑病(PML)和中枢神经系统(CNS)肿瘤。他在接受大剂量类固醇的经验性治疗或适当的肝性脑病治疗后病情没有好转。再次腰椎穿刺进行脑脊液检查发现,约翰-坎宁安(JC)病毒 PCR 检测呈阳性,确诊为 PML。虽然患者没有任何已知的明显免疫抑制症状或治疗,但肝硬化和年龄使他面临着JC病毒中枢神经系统再激活的更高风险。在已发表的 PML 患者病例系列中,没有典型的免疫抑制症状,其中包括几名同时患有肝硬化的患者,与已知的、可逆的免疫抑制原因的患者相比,预后要差得多。
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来源期刊
Neurohospitalist
Neurohospitalist CLINICAL NEUROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
108
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