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一名HIV阴性、免疫功能正常患者的进行性多灶性白质脑病

Progressive Multifocal Leukoencephalopathy in a HIV Negative, Immunocompetent Patient.

作者信息

Nanda T

机构信息

Columbia College of Physicians and Surgeons, Columbia University Medical Center, 161 Fort Washington Avenue, New York, NY 10032, USA.

出版信息

Case Rep Neurol Med. 2016;2016:7050613. doi: 10.1155/2016/7050613. Epub 2016 Jul 27.

Abstract

Progressive multifocal leukoencephalopathy (PML) is a rare demyelinating disease most common in immunodeficient patients. It occurs due to reactivation of the John Cunningham Virus (JCV) and carries a poor prognosis, with a median life expectancy of 6 months. We report a case of a 66-year-old man with a history of HCV related cirrhosis (HCV) and hepatocellular carcinoma (HCC) who was found to have PML in the setting of a negative viral load in the CSF and a CD4+ >200. He initially presented with two weeks of mild confusion and word-finding difficulty concerning for hepatic encephalopathy. An MRI was notable for extensive T2/FLAIR hyperintensity signal in the left temporal lobe. Brain biopsy was positive for JCV. PML is rare in immunocompetent individuals, especially in the setting of a negative viral load. It is possible, however, that transient states of immunosuppression may have been responsible in this case. Although viral load was reported as negative, virus may still have been detected but was below the quantifiable threshold. It is important for clinicians to note that a negative result does not necessarily exclude the possibility of PML, and care should be taken to review lab values on viral load in closer detail.

摘要

进行性多灶性白质脑病(PML)是一种罕见的脱髓鞘疾病,在免疫缺陷患者中最为常见。它是由约翰·坎宁安病毒(JCV)重新激活引起的,预后较差,中位预期寿命为6个月。我们报告一例66岁男性病例,该患者有丙型肝炎病毒相关肝硬化(HCV)和肝细胞癌(HCC)病史,在脑脊液病毒载量阴性且CD4 +>200的情况下被发现患有PML。他最初表现为两周的轻度意识模糊和找词困难,怀疑为肝性脑病。MRI显示左颞叶有广泛的T2/FLAIR高信号。脑活检JCV呈阳性。PML在免疫功能正常的个体中很少见,尤其是在病毒载量阴性的情况下。然而,在这种情况下,短暂的免疫抑制状态可能是原因。尽管报告病毒载量为阴性,但仍可能检测到病毒,只是低于可量化阈值。临床医生应注意,阴性结果不一定排除PML的可能性,应仔细复查病毒载量的实验室值。

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