Case Report: Barely Able to Speak, Can't Stop Echoing: Echolalic Dynamic Aphasia in Progressive Supranuclear Palsy

The diagnostic criteria for progressive supranuclear palsy (PSP) incorporate two speech-language disturbances (SLDs), non-fluent/agrammatic primary progressive aphasia and progressive apraxia of speech, but overlook the inclusion of other SLDs, including dynamic aphasia (DA). Thus, there is a need t...

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Detalhes bibliográficos
Autores: Berthier, Marcelo L., Hoet, Florencia, Beltrán-Corbellini, Álvaro, Santana-Moreno, Daniel, Edelkraut, Lisa, Dávila, Guadalupe
Formato: artículo
Fecha de publicación:2021
País:España
Recursos:Instituto de Salud Carlos III (ISCIII)
Repositorio:Repisalud
Idioma:inglés
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/18332
Acesso em linha:http://hdl.handle.net/20.500.12105/18332
Access Level:acceso abierto
Palavra-chave:Dynamic aphasia
Echolalia
Progressive supranuclear palsy
Primary progressive aphasia
Inhibition deficits
Apathy
Comprehension
Atrophy
Afasia
Ecolalia
Parálisis supranuclear progresiva
Afasia progresiva primaria
Apatía
Comprensión
Atrofia
Patología del habla y lenguaje
Humans
Aged
Supranuclear Palsy, Progressive
Speech
Caudate Nucleus
Neuropsychological Tests
Aphasia
Aphasia, Primary Progressive
Magnetic Resonance Imaging
Frontal Lobe
Tegmentum Mesencephali
Phenotype
Neuroimaging
Apraxias
Speech-Language Pathology
Descrição
Resumo:The diagnostic criteria for progressive supranuclear palsy (PSP) incorporate two speech-language disturbances (SLDs), non-fluent/agrammatic primary progressive aphasia and progressive apraxia of speech, but overlook the inclusion of other SLDs, including dynamic aphasia (DA). Thus, there is a need to reappraise the broad spectrum of SLDs in PSP to include other presenting phenotypes. Here we report findings from the study of two elderly patients with PSP presenting with DA and irrepressible echolalia. Both patients had markedly impoverished verbal production, but their performance in other tasks (repetition and naming) and auditory comprehension were preserved or only mildly impaired. Experimental tests of DA revealed impaired word and sentence generation in response to verbal and non-verbal stimuli. Additional language and cognitive testing revealed different types of echolalia (mitigated, automatic, and echoing approval) as well as impaired inhibitory control and social cognition (mentalizing). Both patients had negative neuropsychiatric alterations (i.e., apathy, aspontaneity, and indifference/emotional flatness). Brain magnetic resonance imaging in both patients showed atrophy of the midbrain tegmentum and superior medial frontal cortex suggestive of PSP, yet further evaluation of the neural correlates using multimodal neuroimaging and neuropathological data was not performed. However, based on the already known neural basis of DA and echolalia in PSP and stroke, we suggest that, in the present cases, neurodegeneration in the midbrain tegmentum, superior medial frontal lobe, and caudate nucleus was responsible for DA and that decreased activity in these regions may play a permissive role for eliciting verbal echoing via disinhibition of the perisylvian speech-language network.