Department of Neurology, Daping Hospital, Army Medical University, Chongqing, 400042, People's Republic of China.
J Neurovirol. 2022 Dec;28(4-6):616-618. doi: 10.1007/s13365-022-01092-1. Epub 2022 Aug 17.
Progressive multifocal leukoencephalopathy (PML) is a rare and potentially fatal demyelinating disease of the central nervous system (CNS) caused by JC virus; it was previously seen predominantly in immunocompromised patients and those under intense immune suppression. Here, we report the case of a patient with PML with hypogammaglobulinemia and a heterozygous mutation in the TCF3 gene. As the TCF3 gene has been demonstrated to play an important role in the B cell differentiation process and the patient had no other medical history of the immune system, he was diagnosed with common variable immunodeficiency (CVID). To our knowledge, this is the first case of patient with a TCF3 gene deficiency and hypogammaglobulinemia who developed PML.
进行性多灶性白质脑病(PML)是一种由 JC 病毒引起的中枢神经系统(CNS)罕见且潜在致命的脱髓鞘疾病;以前主要见于免疫功能低下的患者和接受强烈免疫抑制的患者。在这里,我们报告了一例伴有低丙种球蛋白血症和 TCF3 基因突变的杂合子的 PML 患者。由于 TCF3 基因已被证明在 B 细胞分化过程中发挥重要作用,且患者无其他免疫系统的病史,因此被诊断为普通可变免疫缺陷(CVID)。据我们所知,这是首例 TCF3 基因缺陷和低丙种球蛋白血症患者发生 PML 的病例。