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Title

Creutzfeldt-Jakob disease revealed by a logopenic variant of primary progressive aphasia

Authors
Martory, M D
Roth, S
Neumann, M
Published in European Neurology. 2012, vol. 67, no. 6, p. 360-2
Abstract Logopenic aphasia, mainly characterized by word anomia, sentence and phrase comprehension difficulties secondary to phonological loop deficits but relatively preserved single word comprehension and no agrammatism, is one of the 3 main variants of primary progressive aphasia (PPA). We describe the first case of PPA that fulfilled clinical criteria of logopenic aphasia but showed abnormal DWI hyperintensities that were predominant on the left hemisphere and compatible with Creutzfeldt-Jakob disease (CJD). After abnormally long isolated language deficits, the patient rapidly worsened and died. Autopsy performed 18 months after onset of language difficulties confirmed the diagnosis. We therefore advocate performing DWI sequences in any suspicion of PPA in order to rule out CJD.
Keywords Aphasia, Primary Progressive/classification/diagnosis/etiologyComprehension/physiologyCreutzfeldt-Jakob Syndrome/complicationsDiffusion Magnetic Resonance ImagingFemaleFunctional LateralityHumansLanguageMiddle AgedNeuropsychological TestsTemporal Lobe/pathology
Identifiers
PMID: 22614571
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Research groups Métastases du foie (657)
Neuropsychologie et neurologie comportementale (951)
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MARTORY, M D et al. Creutzfeldt-Jakob disease revealed by a logopenic variant of primary progressive aphasia. In: European Neurology, 2012, vol. 67, n° 6, p. 360-2. https://archive-ouverte.unige.ch/unige:28690

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Deposited on : 2013-06-25

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