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1.
Brain Inj ; 25(12): 1212-20, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21961575

RESUMEN

OBJECTIVE: The purpose of this study was to highlight a speech expression disorder considered as a mixed speech apraxia (SA) and dysarthria syndrome in patients with chronic severe diffuse brain injury (DBI) and to determine its correlation with anatomical localizations of brain lesions using neuroimaging. METHODS: Among 140 patients with chronic severe DBI, eight showed this type of speech disorder. MRI (five patients) and FDG-PET (six patients) procedures were performed. RESULTS: Affected patients could comprehend verbally, read words silently and express words using a word board. Compared with SA, the disorder is characterized by similarities in regards to reduced phonation and marked facio-oral apraxia, but by distinct differences in terms of an accompanying dysphagia and pyramidal/extra-pyramidal symptoms that are similar to symptoms associated with dysarthria due to pseudobulbar palsy. Diffuse regions of the white matter including the left arcuate fasciculus (AF) were significantly decreased in fractional anisotropy value. However, there was no significant cortical metabolic damage in FDG-PET. CONCLUSIONS: The observed speech disorder in these patients is a characteristic entity related to dysfunction of speech expression and may be attributable to damage of not only the AF but also a number of fibres that are related to dysarthria, cognitive and emotional impairments and pyramidal/extra-pyramidal symptoms.


Asunto(s)
Lesiones Encefálicas/patología , Lesiones Encefálicas/fisiopatología , Imagen de Difusión Tensora , Disartria/patología , Disartria/fisiopatología , Estado Vegetativo Persistente/complicaciones , Tomografía de Emisión de Positrones , Adulto , Lesiones Encefálicas/complicaciones , Lesiones Encefálicas/diagnóstico por imagen , Medios de Contraste , Disartria/diagnóstico por imagen , Disartria/etiología , Fluorodesoxiglucosa F18 , Humanos , Masculino , Estado Vegetativo Persistente/patología , Estado Vegetativo Persistente/fisiopatología , Tomografía de Emisión de Positrones/métodos , Índice de Severidad de la Enfermedad
2.
Brain Dev ; 39(6): 493-505, 2017 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-28159458

RESUMEN

OBJECTIVE: This study aimed to investigate the relationship between the change of language symptoms and the change of regional cerebral blood flow (rCBF) in the recovery process of two children with acquired aphasia caused by infarctions from Moyamoya disease with an onset age of 8years. METHODS: We compared the results for the Standard Language Test of Aphasia (SLTA) with rCBF changes in 7 language regions in the left hemisphere and their homologous regions in the right hemisphere at 4 time points from 3weeks for up to 5years after the onset of aphasia, while controlling for the effect of age. RESULTS: In both cases, strong correlations were seen within a hemisphere between adjacent regions or regions that are connected by neuronal fibers, and between some language regions in the left hemisphere and their homologous regions in the right hemisphere. Conversely, there were differences between the two cases in the time course of rCBF changes during their recovery process. CONCLUSION: Consistent with previous studies, the current study suggested that both hemispheres were involved in the long-term recovery of language symptoms in children with acquired aphasia. We suggest that the differences between both cases during their recovery process might be influenced by the brain states before aphasia, by which hemisphere was affected, and by the timing of the surgical revascularization procedure. However, the changes were observed in the data obtained for rCBF with strong correlations with the changes in language performance, so it is possible that rCBF could be used as a biomarker for language symptom changes.


Asunto(s)
Afasia/fisiopatología , Circulación Cerebrovascular/fisiología , Recuperación de la Función/fisiología , Adolescente , Afasia/diagnóstico por imagen , Encéfalo/diagnóstico por imagen , Encéfalo/patología , Niño , Cisteína/análogos & derivados , Cisteína/farmacocinética , Femenino , Humanos , Imagen por Resonancia Magnética , Compuestos de Organotecnecio/farmacocinética , Índice de Severidad de la Enfermedad , Tomografía Computarizada de Emisión de Fotón Único
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