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 |
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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. |
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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.</description><identifier>ISSN: 0014-3022</identifier><identifier>EISSN: 1421-9913</identifier><identifier>DOI: 10.1159/000342220</identifier><identifier>PMID: 23445572</identifier><identifier>CODEN: EUNEAP</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>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</subject><ispartof>European neurology, 2013-01, Vol.69 (5), p.270-274</ispartof><rights>2013 S. Karger AG, Basel</rights><rights>Copyright © 2013 S. Karger AG, Basel.</rights><rights>Copyright (c) 2013 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c327t-d43e8e7970f8464e2a6279a7c356aa961aa6150c7702fb9002b6404b0fc5a3993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2427,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23445572$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ishihara, Kenji</creatorcontrib><creatorcontrib>Araki, Shigeo</creatorcontrib><creatorcontrib>Ihori, Nami</creatorcontrib><creatorcontrib>Suzuki, Yoshio</creatorcontrib><creatorcontrib>Shiota, Jun-ichi</creatorcontrib><creatorcontrib>Arai, Nobutaka</creatorcontrib><creatorcontrib>Nakano, Imaharu</creatorcontrib><creatorcontrib>Kawamura, Mitsuru</creatorcontrib><title>Pseudobulbar Dysarthria in the Initial Stage of Motor Neuron Disease with Dementia: A Clinicopathological Report of Two Autopsied Cases</title><title>European neurology</title><addtitle>Eur Neurol</addtitle><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.</description><subject>Aged</subject><subject>Autopsy</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Dementia</subject><subject>Dementia - complications</subject><subject>Dementia - diagnosis</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Middle Aged</subject><subject>Motor Neuron Disease - complications</subject><subject>Motor Neuron Disease - diagnosis</subject><subject>Original Paper</subject><subject>Pseudobulbar Palsy - diagnosis</subject><subject>Pseudobulbar Palsy - etiology</subject><subject>Retrospective Studies</subject><subject>RNA-Binding Protein FUS - metabolism</subject><subject>Staining and Labeling</subject><subject>Tomography, Emission-Computed, Single-Photon</subject><issn>0014-3022</issn><issn>1421-9913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqN0c2LEzEYx_EgiltXD95FAl7cw2je03grrasL6wu6nodnps-0WaeTMcmw7F_gv21Kaw-ePIXAJ18IP0Kec_aGc-3eMsakEkKwB2TGleCVc1w-JDPGuKokE-KMPEnptly1s_PH5ExIpbS2YkZ-f004rUMz9Q1EurpPEPM2eqB-oHmL9Grw2UNPv2fYIA0d_RRyiPQzTjEMdOUTQkJ65_OWrnCHQ8Hv6IIuez_4NoyQt6EPG9-WxDccQ8z7xs1doIsphzF5XNNlKaSn5FEHfcJnx_Oc_Lh8f7P8WF1_-XC1XFxXrRQ2V2slcY7WWdbNlVEowAjrwLZSGwBnOIDhmrXWMtE1jjHRGMVUw7pWg3ROnpPXh-4Yw68JU653PrXY9zBgmFLNpRVMc_NfVBu5h3v66h96G6Y4lI8UZaw2WklW1MVBtTGkFLGrx-h3EO9rzur9kPVpyGJfHotTs8P1Sf5droAXB_AT4gbjCRzf_wHBtp-f</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Ishihara, Kenji</creator><creator>Araki, Shigeo</creator><creator>Ihori, Nami</creator><creator>Suzuki, Yoshio</creator><creator>Shiota, Jun-ichi</creator><creator>Arai, Nobutaka</creator><creator>Nakano, Imaharu</creator><creator>Kawamura, Mitsuru</creator><general>S. 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Araki, Shigeo ; Ihori, Nami ; Suzuki, Yoshio ; Shiota, Jun-ichi ; Arai, Nobutaka ; Nakano, Imaharu ; Kawamura, Mitsuru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-d43e8e7970f8464e2a6279a7c356aa961aa6150c7702fb9002b6404b0fc5a3993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aged</topic><topic>Autopsy</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - metabolism</topic><topic>Brain - pathology</topic><topic>Dementia</topic><topic>Dementia - complications</topic><topic>Dementia - diagnosis</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Middle Aged</topic><topic>Motor Neuron Disease - complications</topic><topic>Motor Neuron Disease - diagnosis</topic><topic>Original Paper</topic><topic>Pseudobulbar Palsy - diagnosis</topic><topic>Pseudobulbar Palsy - etiology</topic><topic>Retrospective Studies</topic><topic>RNA-Binding Protein FUS - metabolism</topic><topic>Staining and Labeling</topic><topic>Tomography, Emission-Computed, Single-Photon</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ishihara, Kenji</creatorcontrib><creatorcontrib>Araki, Shigeo</creatorcontrib><creatorcontrib>Ihori, Nami</creatorcontrib><creatorcontrib>Suzuki, Yoshio</creatorcontrib><creatorcontrib>Shiota, Jun-ichi</creatorcontrib><creatorcontrib>Arai, Nobutaka</creatorcontrib><creatorcontrib>Nakano, Imaharu</creatorcontrib><creatorcontrib>Kawamura, Mitsuru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>European neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ishihara, Kenji</au><au>Araki, Shigeo</au><au>Ihori, Nami</au><au>Suzuki, Yoshio</au><au>Shiota, Jun-ichi</au><au>Arai, Nobutaka</au><au>Nakano, Imaharu</au><au>Kawamura, Mitsuru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pseudobulbar Dysarthria in the Initial Stage of Motor Neuron Disease with Dementia: A Clinicopathological Report of Two Autopsied Cases</atitle><jtitle>European neurology</jtitle><addtitle>Eur Neurol</addtitle><date>2013-01-01</date><risdate>2013</risdate><volume>69</volume><issue>5</issue><spage>270</spage><epage>274</epage><pages>270-274</pages><issn>0014-3022</issn><eissn>1421-9913</eissn><coden>EUNEAP</coden><abstract>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.</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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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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