RÉSUMÉ
Resumen: En la fisiopatología de la enfermedad de Alzheimer durante mucho tiempo se ha dado mayor importancia al estudio del beta amiloide. A la luz de los conocimientos actuales también debe considerarse la participación de las vías de cinasas activadas por el receptor de insulina a nivel neuronal y particularmente a nivel del hipocampo.
Abstract: In the pathophysiology of Alzheimer's disease, the study of amyloid beta has long been of great importance. In light of current knowledge, the involvement of insulin receptor activated kinase pathways at the neuronal level and particularly at the hippocampus levels should also be considered.
RÉSUMÉ
BACKGROUND: Non-fluent agrammatic primary progressive aphasia (naPPA) is characterized by progressive non-fluent speech disorder and might be associated with taupathy such as corticobasal degeneration (CBD) and progressive supranuclear palsy. We report a case of overlap syndrome presented with language impairment, and diagnosed as naPPA with possible CBD. CASE REPORT: A 58-year-old woman visited a memory and dementia clinic, with a 10-month history of progressive language disturbance. She was diagnosed as naPPA and overlapping CBD, based on the clinical features and neuroimaging findings including florbetaben PET. CONCLUSIONS: naPPA is pathologically caused by taupathy, and might progress to asymmetrical parkinsonism and apraxia, suggestive of CBD. Overlapping clinical features in our case represent various phenotypes of taupathy.
Sujet(s)
Femelle , Humains , Adulte d'âge moyen , Aphasie progressive primaire , Apraxies , Démence , Mémoire , Neuroimagerie , Syndromes parkinsoniens , Phénotype , Paralysie supranucléaire progressiveRÉSUMÉ
BACKGROUND: Tauopathies are a group of diseases caused by the accumulation of hyperphosphorylated tau protein in the central nervous system. Previous studies have revealed that there is considerable overlap in clinical, pathological, and genetic features among different taupathies. CASE REPORT: We report a patient with non-fluent/agrammatic primary progressive aphasia at the initial assessment. Over time, other symptoms belonging to corticobasal degeneration and progressive supranuclear palsy appeared in this patient. CONCLUSIONS: Clinical overlapping features in these disorders may represent different phenotypes of a single disease process.