| Literature DB >> 27273076 |
Jessie Grewal1, Poorvi Dalal1, Michelle Bowman1,2, Behiye Kaya3, José Javier Otero3, Jaime Imitola4,5,6.
Abstract
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.Entities:
Keywords: Immunocompetent host; Progressive multifocal leukoencephalopathy
Mesh:
Year: 2016 PMID: 27273076 DOI: 10.1007/s13365-016-0459-y
Source DB: PubMed Journal: J Neurovirol ISSN: 1355-0284 Impact factor: 2.643