| Literature DB >> 24515530 |
Louis Dang1, Xin Dang2, Igor J Koralnik2, Peter K Todd1.
Abstract
IMPORTANCE: Progressive multifocal leukoencephalopathy results from lytic infection of the glia by the JC polyomavirus (JCV); JCV granule cell neuronopathy is caused by infection with a mutated form of JCV, leading to a shift in viral tropism from the glia to cerebellar granule cells. This shift results in a clinical syndrome dominated by progressive cerebellar dysfunction that might elude standard diagnostic workup strategies for ataxia. OBSERVATIONS: We present the case report of a patient receiving long-term rituximab therapy who developed progressive cerebellar ataxia and marked isolated cerebellar degeneration. This syndrome resulted from JCV granule cell neuronopathy associated with a novel JCV mutation. CONCLUSIONS AND RELEVANCE: New onset or worsening of isolated cerebellar ataxia in patients being treated with rituximab or natalizumab warrants early assessment for JCV infection.Entities:
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Year: 2014 PMID: 24515530 PMCID: PMC4086309 DOI: 10.1001/jamaneurol.2013.4668
Source DB: PubMed Journal: JAMA Neurol ISSN: 2168-6149 Impact factor: 18.302