Mixed tau and TDP-43 pathology in a patient with unclassifiable primary progressive aphasia

Research output: Contribution to journalArticle

5 Scopus citations

Abstract

Classifying primary progressive aphasia (PPA) into variants that may predict the underlying pathology is important. However, some PPA patients cannot be classified. A 78-year-old woman had unclassifiable PPA characterized by anomia, dysarthria, and apraxia of speech without agrammatism. Magnetic resonance imaging revealed left mesial temporal atrophy and 18-flourodeoxy-glucose positron emission tomography showed left anterior temporal and posterior frontal (premotor) hypometabolism. Autopsy revealed a mixed tauopathy (argyrophilic grain disease) and transactive response-DNA-binding-protein-43 proteinopathy. Dual pathologies may explain the difficulty classifying some PPA patients and recognizing this will be important as new imaging techniques (particularly tau-positron emission tomography) are introduced and patients begin enrollment in clinical trials targeting the underlying proteinopathy.

Original languageEnglish (US)
Pages (from-to)55-59
Number of pages5
JournalNeurocase
Volume22
Issue number1
DOIs
StatePublished - Jan 2 2016

Keywords

  • argyrophilic grain disease
  • frontotemporal lobar degeneration
  • primary progressive aphasia
  • tau
  • TDP-43

ASJC Scopus subject areas

  • Clinical Neurology
  • Arts and Humanities (miscellaneous)

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