Pseudobulbar Dysarthria in the Initial Stage of Motor Neuron Disease with Dementia: A Clinicopathological Report of Two Autopsied Cases

We retrospectively analyzed the clinical features of two cases of neurodegenerative disease, whose initial symptoms were motor speech disorder and dementia, brought to autopsy. We compared the distributions of pathological findings with the clinical features. The main symptom of speech disorder was...

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Veröffentlicht in:European neurology 2013-01, Vol.69 (5), p.270-274
Hauptverfasser: Ishihara, Kenji, Araki, Shigeo, Ihori, Nami, Suzuki, Yoshio, Shiota, Jun-ichi, Arai, Nobutaka, Nakano, Imaharu, Kawamura, Mitsuru
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container_end_page 274
container_issue 5
container_start_page 270
container_title European neurology
container_volume 69
creator Ishihara, Kenji
Araki, Shigeo
Ihori, Nami
Suzuki, Yoshio
Shiota, Jun-ichi
Arai, Nobutaka
Nakano, Imaharu
Kawamura, Mitsuru
description We retrospectively analyzed the clinical features of two cases of neurodegenerative disease, whose initial symptoms were motor speech disorder and dementia, brought to autopsy. We compared the distributions of pathological findings with the clinical features. The main symptom of speech disorder was dysarthria, involving low pitch, slow rate, hypernasality and hoarseness. Other than these findings, effortful speech, sound prolongation and initial difficulty were observed. Moreover, repetition of multisyllables was severely impaired compared to monosyllables. Repetition and comprehension of words and sentences were not impaired. Neither atrophy nor fasciculation of the tongue was observed. Both cases showed rapid progression to mutism within a few years. Neuropathologically, frontal lobe degeneration including the precentral gyrus was observed. The bilateral pyramidal tracts also showed severe degeneration. However, the nucleus of the hypoglossal nerve showed only mild degeneration. These findings suggest upper motor neuron dominant motor neuron disease with dementia. We believe the results indicate a subgroup of motor neuron disease with dementia whose initial symptoms involve pseudobulbar palsy and dementia, and which shows rapid progression to mutism.
doi_str_mv 10.1159/000342220
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We believe the results indicate a subgroup of motor neuron disease with dementia whose initial symptoms involve pseudobulbar palsy and dementia, and which shows rapid progression to mutism.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>23445572</pmid><doi>10.1159/000342220</doi><tpages>5</tpages></addata></record>
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ispartof European neurology, 2013-01, Vol.69 (5), p.270-274
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source MEDLINE; Karger Journals
subjects Aged
Autopsy
Brain - diagnostic imaging
Brain - metabolism
Brain - pathology
Dementia
Dementia - complications
Dementia - diagnosis
DNA-Binding Proteins - metabolism
Female
Humans
Magnetic Resonance Imaging
Middle Aged
Motor Neuron Disease - complications
Motor Neuron Disease - diagnosis
Original Paper
Pseudobulbar Palsy - diagnosis
Pseudobulbar Palsy - etiology
Retrospective Studies
RNA-Binding Protein FUS - metabolism
Staining and Labeling
Tomography, Emission-Computed, Single-Photon
title Pseudobulbar Dysarthria in the Initial Stage of Motor Neuron Disease with Dementia: A Clinicopathological Report of Two Autopsied Cases
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