Division of Neurology, The Children's Hospital of Philadelphia, Philadelphia, PA 19146, USA.
J Neurovirol. 2011 Oct;17(5):500-3. doi: 10.1007/s13365-011-0045-2. Epub 2011 Jul 23.
Progressive multifocal leukoencephalopathy (PML) is a severe demyelinating disease of the central nervous system (CNS) caused by lytic infection of oligodendrocytes by the polyomavirus JC (JCV). PML has classically been described in individuals with profound cellular immunosuppression. While some case reports have documented PML in individuals with minimal or occult immunosuppression, such cases are very rare and their pathogenesis is not well understood. We report a unique case of a 74 year-old woman who developed PML clinically mimicking tumefactive multiple sclerosis in the context of an idiopathic isolated CD8+ T-lymphocytopenia. Her course subsequently stabilized, concomitant to the development of a cellular immune response directed against JCV. We review the current literature of related cases and discuss the pathogenesis and implications of this rare presentation.
进行性多灶性白质脑病(PML)是一种由多瘤病毒 JC(JCV)溶细胞性感染少突胶质细胞引起的严重中枢神经系统(CNS)脱髓鞘疾病。PML 经典地发生在严重细胞免疫抑制的个体中。虽然一些病例报告记录了在免疫抑制最小或隐匿的个体中发生 PML,但这种情况非常罕见,其发病机制尚不清楚。我们报告了一例独特的病例,一名 74 岁女性在特发性孤立性 CD8+T 淋巴细胞减少症的背景下出现 PML,临床表现类似于肿块样多发性硬化症。随着针对 JCV 的细胞免疫反应的发展,她的病情随后稳定下来。我们回顾了相关病例的现有文献,并讨论了这种罕见表现的发病机制和意义。