Progressive multifocal leukoencephalopathy in a patient without apparent immunosuppression

被引:15
作者
Grewal, Jessie [1 ]
Dalal, Poorvi [1 ]
Bowman, Michelle [1 ,2 ]
Kaya, Behiye [3 ]
Otero, Jose Javier [3 ]
Imitola, Jaime [1 ,2 ,4 ]
机构
[1] Ohio State Univ, Dept Neurol, Wexner Med Ctr, Columbus, OH 43210 USA
[2] Ohio State Univ, Comprehens Multiple Sclerosis Ctr, Wexner Med Ctr, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Pathol, Wexner Med Ctr, Columbus, OH 43210 USA
[4] Ohio State Univ, Div Neuroimmunol & Multiple Sclerosis, Lab Neural Stem Cells & Funct Neurogenet, Wexner Med Ctr, 460W12th Ave,Biomed Res Tower,Room 688, Columbus, OH 43321 USA
关键词
Progressive multifocal leukoencephalopathy; Immunocompetent host; IDIOPATHIC CD4 LYMPHOCYTOPENIA; JC-VIRUS; MONOCLONAL-ANTIBODY; PML; PATHOGENESIS; ANTIGEN; DISEASE; SV40;
D O I
10.1007/s13365-016-0459-y
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Progressive multifocal leukoencephalopathy (PML) is a viral demyelinating disease due to the reactivation of the JC virus (JCV), which usually occurs in the context of immunosuppression in HIV infection, malignancy, or in patients on disease modifying therapy for autoimmune diseases, such as multiple sclerosis (MS) and Crohn's disease. Notably, there is growing recognition that PML can occur in patients with transient immune dysfunction. Here, we present a case of a 55-year-old man without history of immunosuppression or evidence of ICL who was diagnosed with PML on brain biopsy. We will discuss the potential etiologies of mild and transient immunosuppression that can lead to PML with non-apparent immunosuppression.
引用
收藏
页码:683 / 687
页数:5
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