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一名肝硬化和肝细胞癌患者的进行性多灶性白质脑病

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

作者信息

Caliendo Eric, Williams Sally, Hutto Spencer, Massart Annie, Burlock Brianna, Weinberg Brent, Cavanagh Julien, Shi Hang

机构信息

Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA.

Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA.

出版信息

Neurohospitalist. 2024 Oct;14(4):441-445. doi: 10.1177/19418744241259072. Epub 2024 Jun 3.

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.

摘要

以下病例描述了一名73岁男性的一系列进行性认知和运动功能缺陷,该患者患有肝硬化且有局限于肝脏的早期肝细胞癌病史。他存在计算、语言和书写方面的缺陷,以及轻微的右侧肢体无力。脑部磁共振成像(MRI)显示双侧顶叶和左侧枕颞叶区域有非强化性白质病变,无占位效应,与神经系统检查结果相符。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性和脱髓鞘性疾病、肝性脑病、后部可逆性脑病综合征、进行性多灶性白质脑病(PML)和中枢神经系统(CNS)肿瘤。经验性使用高剂量类固醇治疗或充分的肝性脑病治疗后,他的病情并未改善。再次进行腰椎穿刺以进行额外的脑脊液检查,结果显示约翰·坎宁安(JC)病毒PCR检测呈阳性,确诊为PML。尽管该患者没有任何已知的明显免疫抑制状况或治疗,但他的肝硬化和年龄使他发生JC病毒中枢神经系统再激活的风险更高。在一个已发表的PML病例系列中,患者没有典型的免疫抑制状况,其中包括几名伴有肝硬化的患者,与那些有已知的、可逆性免疫抑制原因的患者相比,预后要差得多。

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