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Progressive multifocal leukoencephalopathy in a patient with Good's syndrome.
- Source :
-
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases [Int J Infect Dis] 2010 May; Vol. 14 (5), pp. e444-7. Date of Electronic Publication: 2009 Aug 19. - Publication Year :
- 2010
-
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.<br /> (Copyright 2009 International Society for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.)
- Subjects :
- Aged
Brain pathology
Fatal Outcome
Female
Humans
Immunohistochemistry
Immunologic Deficiency Syndromes pathology
Leukoencephalopathy, Progressive Multifocal pathology
Leukoencephalopathy, Progressive Multifocal virology
Immunologic Deficiency Syndromes complications
JC Virus isolation & purification
Leukoencephalopathy, Progressive Multifocal complications
Subjects
Details
- Language :
- English
- ISSN :
- 1878-3511
- Volume :
- 14
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
- Publication Type :
- Academic Journal
- Accession number :
- 19695918
- Full Text :
- https://doi.org/10.1016/j.ijid.2009.06.005