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Progressive multifocal leukoencephalopathy in a patient with Good's syndrome
Authors:Giovanna Squintani  Sergio Ferrari  Elena Bazzoli  Roberto Eleopra  Carlo La Monaca  Enrico Cagliari  Gianluigi Zanusso  Maria Cristina Mantovan  Salvatore Monaco
Affiliation:1. Neurology Unit, Ospedale Civile Maggiore, Piazzale Stefani, 1, 37134, Verona, Italy;2. Department of Neurological and Visual Sciences, Section of Clinical Neurology, University of Verona, Verona, Italy;3. Neurology Unit, Department of Neurological Sciences, Ospedale dell’Angelo, Mestre Venice, Italy;4. Neuroradiology Unit, Department of Neurological Sciences, Ospedale dell’Angelo, Mestre Venice, Italy
Abstract:Good's syndrome (GS) is an immunodeficiency characterized by thymoma, hypogammaglobulinemia, and impaired T-cell function. The clinical manifestations of GS include recurrent or chronic infections from common or opportunistic pathogens. Encephalitis is a rare event, with only anecdotal reports of cytomegalovirus infection. Herein we report the case of a 79-year-old woman with GS who developed subacute motor deficits and cognitive changes. Magnetic resonance imaging (MRI) of the brain disclosed white- and gray-matter lesions, mostly in the right frontal and parietal areas. Polyoma virus JC, the agent of progressive multifocal encephalopathy (PML), was identified in cerebrospinal fluid samples and brain biopsy specimens. After diagnosis, the disease had a rapid fatal course. The present case represents the first reported association between GS and PML.
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