Sequential MRI in a case of Creutzfeldt-Jakob disease
A 48-year-old man suddenly developed clinically and electroencephalographically nonspecific dementia. On MRI sequences, only diffusion-weighted images (DWI) of the cortex were unequivocally pathological. Obvious atrophy and basal ganglia signal changes appeared only 9 months after the onset. Brain b...
Gespeichert in:
Veröffentlicht in: | Neuroradiology 2002-03, Vol.44 (3), p.223-226 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 226 |
---|---|
container_issue | 3 |
container_start_page | 223 |
container_title | Neuroradiology |
container_volume | 44 |
creator | TRIBL, G. G STRASSER, G ZEITLHOFER, J ASENBAUM, S JARIUS, C WESSELY, P PRAYER, D |
description | A 48-year-old man suddenly developed clinically and electroencephalographically nonspecific dementia. On MRI sequences, only diffusion-weighted images (DWI) of the cortex were unequivocally pathological. Obvious atrophy and basal ganglia signal changes appeared only 9 months after the onset. Brain biopsy confirmed Creutzfeldt-Jakob disease (CJD). In rapidly progressive dementia, we recommend DWI for early diagnosis of CJD. |
doi_str_mv | 10.1007/s002340100695 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71598953</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>691995471</sourcerecordid><originalsourceid>FETCH-LOGICAL-c346t-b818975506db03b4fbbe578a5752646bc57bd8361288c344a27d65a97dc14f523</originalsourceid><addsrcrecordid>eNpd0EtLxDAQB_AgiruuHr1KEfRWnbyToyw-VlYEH-eSpCl07bZr0h700xvZwqKnGZhfhskfoVMMVxhAXkcAQhmkXmi-h6aYUZJjTWAfTdNI5VQzmKCjGFcAQCWVh2iCsWaESjFF_NV_Dr7ta9NkTy-LrG4zkzkTfdZV2Tz4of-ufFP2-aP56GxW1tGn4TE6qEwT_clYZ-j97vZt_pAvn-8X85tl7igTfW4VVlpyDqK0QC2rrPVcKsMlJ4IJ67i0paICE6XSC2aILAU3WpYOs4oTOkOX272b0KUzY1-s6-h805jWd0MsJOZaaU4TPP8HV90Q2nRbQQgmFCgXCeVb5EIXY_BVsQn12oSvAkPxG2bxJ8zkz8alg137cqfH9BK4GIGJzjRVMK2r487R9AUmCP0ByLp4AQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>221230356</pqid></control><display><type>article</type><title>Sequential MRI in a case of Creutzfeldt-Jakob disease</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>TRIBL, G. G ; STRASSER, G ; ZEITLHOFER, J ; ASENBAUM, S ; JARIUS, C ; WESSELY, P ; PRAYER, D</creator><creatorcontrib>TRIBL, G. G ; STRASSER, G ; ZEITLHOFER, J ; ASENBAUM, S ; JARIUS, C ; WESSELY, P ; PRAYER, D</creatorcontrib><description>A 48-year-old man suddenly developed clinically and electroencephalographically nonspecific dementia. On MRI sequences, only diffusion-weighted images (DWI) of the cortex were unequivocally pathological. Obvious atrophy and basal ganglia signal changes appeared only 9 months after the onset. Brain biopsy confirmed Creutzfeldt-Jakob disease (CJD). In rapidly progressive dementia, we recommend DWI for early diagnosis of CJD.</description><identifier>ISSN: 0028-3940</identifier><identifier>EISSN: 1432-1920</identifier><identifier>DOI: 10.1007/s002340100695</identifier><identifier>PMID: 11942376</identifier><identifier>CODEN: NRDYAB</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Biological and medical sciences ; Brain - pathology ; Contrast Media ; Creutzfeldt-Jakob Syndrome - diagnosis ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Electroencephalography ; Gadolinium DTPA ; Humans ; Magnetic Resonance Imaging ; Magnetic Resonance Spectroscopy ; Male ; Medical sciences ; Middle Aged ; Neurology ; Time Factors</subject><ispartof>Neuroradiology, 2002-03, Vol.44 (3), p.223-226</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright Springer-Verlag New York, Inc. Mar 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c346t-b818975506db03b4fbbe578a5752646bc57bd8361288c344a27d65a97dc14f523</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13523462$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11942376$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TRIBL, G. G</creatorcontrib><creatorcontrib>STRASSER, G</creatorcontrib><creatorcontrib>ZEITLHOFER, J</creatorcontrib><creatorcontrib>ASENBAUM, S</creatorcontrib><creatorcontrib>JARIUS, C</creatorcontrib><creatorcontrib>WESSELY, P</creatorcontrib><creatorcontrib>PRAYER, D</creatorcontrib><title>Sequential MRI in a case of Creutzfeldt-Jakob disease</title><title>Neuroradiology</title><addtitle>Neuroradiology</addtitle><description>A 48-year-old man suddenly developed clinically and electroencephalographically nonspecific dementia. On MRI sequences, only diffusion-weighted images (DWI) of the cortex were unequivocally pathological. Obvious atrophy and basal ganglia signal changes appeared only 9 months after the onset. Brain biopsy confirmed Creutzfeldt-Jakob disease (CJD). In rapidly progressive dementia, we recommend DWI for early diagnosis of CJD.</description><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Contrast Media</subject><subject>Creutzfeldt-Jakob Syndrome - diagnosis</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Electroencephalography</subject><subject>Gadolinium DTPA</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Time Factors</subject><issn>0028-3940</issn><issn>1432-1920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpd0EtLxDAQB_AgiruuHr1KEfRWnbyToyw-VlYEH-eSpCl07bZr0h700xvZwqKnGZhfhskfoVMMVxhAXkcAQhmkXmi-h6aYUZJjTWAfTdNI5VQzmKCjGFcAQCWVh2iCsWaESjFF_NV_Dr7ta9NkTy-LrG4zkzkTfdZV2Tz4of-ufFP2-aP56GxW1tGn4TE6qEwT_clYZ-j97vZt_pAvn-8X85tl7igTfW4VVlpyDqK0QC2rrPVcKsMlJ4IJ67i0paICE6XSC2aILAU3WpYOs4oTOkOX272b0KUzY1-s6-h805jWd0MsJOZaaU4TPP8HV90Q2nRbQQgmFCgXCeVb5EIXY_BVsQn12oSvAkPxG2bxJ8zkz8alg137cqfH9BK4GIGJzjRVMK2r487R9AUmCP0ByLp4AQ</recordid><startdate>20020301</startdate><enddate>20020301</enddate><creator>TRIBL, G. G</creator><creator>STRASSER, G</creator><creator>ZEITLHOFER, J</creator><creator>ASENBAUM, S</creator><creator>JARIUS, C</creator><creator>WESSELY, P</creator><creator>PRAYER, D</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QO</scope><scope>7RV</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20020301</creationdate><title>Sequential MRI in a case of Creutzfeldt-Jakob disease</title><author>TRIBL, G. G ; STRASSER, G ; ZEITLHOFER, J ; ASENBAUM, S ; JARIUS, C ; WESSELY, P ; PRAYER, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c346t-b818975506db03b4fbbe578a5752646bc57bd8361288c344a27d65a97dc14f523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Biological and medical sciences</topic><topic>Brain - pathology</topic><topic>Contrast Media</topic><topic>Creutzfeldt-Jakob Syndrome - diagnosis</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Electroencephalography</topic><topic>Gadolinium DTPA</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TRIBL, G. G</creatorcontrib><creatorcontrib>STRASSER, G</creatorcontrib><creatorcontrib>ZEITLHOFER, J</creatorcontrib><creatorcontrib>ASENBAUM, S</creatorcontrib><creatorcontrib>JARIUS, C</creatorcontrib><creatorcontrib>WESSELY, P</creatorcontrib><creatorcontrib>PRAYER, D</creatorcontrib><collection>Pascal-Francis</collection><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>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</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 Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroradiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TRIBL, G. G</au><au>STRASSER, G</au><au>ZEITLHOFER, J</au><au>ASENBAUM, S</au><au>JARIUS, C</au><au>WESSELY, P</au><au>PRAYER, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sequential MRI in a case of Creutzfeldt-Jakob disease</atitle><jtitle>Neuroradiology</jtitle><addtitle>Neuroradiology</addtitle><date>2002-03-01</date><risdate>2002</risdate><volume>44</volume><issue>3</issue><spage>223</spage><epage>226</epage><pages>223-226</pages><issn>0028-3940</issn><eissn>1432-1920</eissn><coden>NRDYAB</coden><abstract>A 48-year-old man suddenly developed clinically and electroencephalographically nonspecific dementia. On MRI sequences, only diffusion-weighted images (DWI) of the cortex were unequivocally pathological. Obvious atrophy and basal ganglia signal changes appeared only 9 months after the onset. Brain biopsy confirmed Creutzfeldt-Jakob disease (CJD). In rapidly progressive dementia, we recommend DWI for early diagnosis of CJD.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>11942376</pmid><doi>10.1007/s002340100695</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0028-3940 |
ispartof | Neuroradiology, 2002-03, Vol.44 (3), p.223-226 |
issn | 0028-3940 1432-1920 |
language | eng |
recordid | cdi_proquest_miscellaneous_71598953 |
source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Biological and medical sciences Brain - pathology Contrast Media Creutzfeldt-Jakob Syndrome - diagnosis Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Electroencephalography Gadolinium DTPA Humans Magnetic Resonance Imaging Magnetic Resonance Spectroscopy Male Medical sciences Middle Aged Neurology Time Factors |
title | Sequential MRI in a case of Creutzfeldt-Jakob disease |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T14%3A22%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Sequential%20MRI%20in%20a%20case%20of%20Creutzfeldt-Jakob%20disease&rft.jtitle=Neuroradiology&rft.au=TRIBL,%20G.%20G&rft.date=2002-03-01&rft.volume=44&rft.issue=3&rft.spage=223&rft.epage=226&rft.pages=223-226&rft.issn=0028-3940&rft.eissn=1432-1920&rft.coden=NRDYAB&rft_id=info:doi/10.1007/s002340100695&rft_dat=%3Cproquest_cross%3E691995471%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=221230356&rft_id=info:pmid/11942376&rfr_iscdi=true |