Movement Disorders (revue)

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Epilepsia partialis continua with dystonic hand movement in a patient with a malformation of cortical development

Identifieur interne : 001533 ( PascalFrancis/Corpus ); précédent : 001532; suivant : 001534

Epilepsia partialis continua with dystonic hand movement in a patient with a malformation of cortical development

Auteurs : Julie Zyss ; Jing Xie-Brustolin ; Philippe Ryvlin ; Stephane Peysson ; Albert Beschet ; Dominique Sappey-Marinier ; Marc Hermier ; Stéphane Thobois

Source :

RBID : Pascal:07-0491129

Descripteurs français

English descriptors

Abstract

Malformations of cortical development (MCD) with polymicrogyria and schizencephaly are due to abnormal cortical organization and usually manifest by intractable epilepsy and mental retardation. Epileptical activity is often hard to register and focal dystonia associated with such MCD has previously been described but without any metabolic imaging. We report here a 46-year-old man presenting with late-onset atypical abnormal movements of his left hand associated with right central region MCD. To demonstrate the involvement of an epileptical focus, we performed [18F]FDG-PET and fMRI both before and after a single dose of clobazam and diazepam, respectively. Characteristics of the abnormal hand movements, clinical response to the medication, and the result of the [18F]FDG-PET and fMRI investigations all favor the diagnosis of epilepsia partialis continua. We conclude that the dystonic movement is part of the partial seizure.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0885-3185
A03   1    @0 Mov. disord.
A05       @2 22
A06       @2 12
A08 01  1  ENG  @1 Epilepsia partialis continua with dystonic hand movement in a patient with a malformation of cortical development
A11 01  1    @1 ZYSS (Julie)
A11 02  1    @1 XIE-BRUSTOLIN (Jing)
A11 03  1    @1 RYVLIN (Philippe)
A11 04  1    @1 PEYSSON (Stephane)
A11 05  1    @1 BESCHET (Albert)
A11 06  1    @1 SAPPEY-MARINIER (Dominique)
A11 07  1    @1 HERMIER (Marc)
A11 08  1    @1 THOBOIS (Stéphane)
A14 01      @1 Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C @2 Lyon @3 FRA @Z 1 aut. @Z 2 aut. @Z 4 aut. @Z 8 aut.
A14 02      @1 Université de Lyon, Hospices Civils de Lyon, CTRS-IDEE, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie Fonctionnelle et d'Epileptologie @2 Lyon @3 FRA @Z 3 aut.
A14 03      @1 Centre Hospitalier Valence, Service de Neurologie @2 Valence @3 FRA @Z 5 aut.
A14 04      @1 Université de Lyon, CERMEP-Imagerie du vivant @2 69677 Bron @3 FRA @Z 6 aut.
A14 05      @1 Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neuroradiologie @2 Lyon @3 FRA @Z 7 aut.
A14 06      @1 INSERM U 864 @2 Bron @3 FRA @Z 8 aut.
A20       @1 1793-1796
A21       @1 2007
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000143464810160
A44       @0 0000 @1 © 2007 INIST-CNRS. All rights reserved.
A45       @0 10 ref.
A47 01  1    @0 07-0491129
A60       @1 P @3 CC
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 Malformations of cortical development (MCD) with polymicrogyria and schizencephaly are due to abnormal cortical organization and usually manifest by intractable epilepsy and mental retardation. Epileptical activity is often hard to register and focal dystonia associated with such MCD has previously been described but without any metabolic imaging. We report here a 46-year-old man presenting with late-onset atypical abnormal movements of his left hand associated with right central region MCD. To demonstrate the involvement of an epileptical focus, we performed [18F]FDG-PET and fMRI both before and after a single dose of clobazam and diazepam, respectively. Characteristics of the abnormal hand movements, clinical response to the medication, and the result of the [18F]FDG-PET and fMRI investigations all favor the diagnosis of epilepsia partialis continua. We conclude that the dystonic movement is part of the partial seizure.
C02 01  X    @0 002B17
C02 02  X    @0 002B17C
C02 03  X    @0 002B17F
C03 01  X  FRE  @0 Système nerveux pathologie @5 01
C03 01  X  ENG  @0 Nervous system diseases @5 01
C03 01  X  SPA  @0 Sistema nervioso patología @5 01
C03 02  X  FRE  @0 Dystonie @5 02
C03 02  X  ENG  @0 Dystonia @5 02
C03 02  X  SPA  @0 Distonía @5 02
C03 03  X  FRE  @0 Main @5 09
C03 03  X  ENG  @0 Hand @5 09
C03 03  X  SPA  @0 Mano @5 09
C03 04  X  FRE  @0 Homme @5 10
C03 04  X  ENG  @0 Human @5 10
C03 04  X  SPA  @0 Hombre @5 10
C03 05  X  FRE  @0 Malformation @5 11
C03 05  X  ENG  @0 Malformation @5 11
C03 05  X  SPA  @0 Malformación @5 11
C07 01  X  FRE  @0 Extrapyramidal syndrome @5 37
C07 01  X  ENG  @0 Extrapyramidal syndrome @5 37
C07 01  X  SPA  @0 Extrapiramidal síndrome @5 37
C07 02  X  FRE  @0 Mouvement involontaire @5 38
C07 02  X  ENG  @0 Involuntary movement @5 38
C07 02  X  SPA  @0 Movimiento involuntario @5 38
C07 03  X  FRE  @0 Muscle strié pathologie @5 39
C07 03  X  ENG  @0 Striated muscle disease @5 39
C07 03  X  SPA  @0 Músculo estriado patología @5 39
C07 04  X  FRE  @0 Trouble neurologique @5 40
C07 04  X  ENG  @0 Neurological disorder @5 40
C07 04  X  SPA  @0 Trastorno neurológico @5 40
C07 05  X  FRE  @0 Encéphale pathologie @5 41
C07 05  X  ENG  @0 Cerebral disorder @5 41
C07 05  X  SPA  @0 Encéfalo patología @5 41
C07 06  X  FRE  @0 Système nerveux central pathologie @5 42
C07 06  X  ENG  @0 Central nervous system disease @5 42
C07 06  X  SPA  @0 Sistema nervosio central patología @5 42
N21       @1 323
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 07-0491129 INIST
ET : Epilepsia partialis continua with dystonic hand movement in a patient with a malformation of cortical development
AU : ZYSS (Julie); XIE-BRUSTOLIN (Jing); RYVLIN (Philippe); PEYSSON (Stephane); BESCHET (Albert); SAPPEY-MARINIER (Dominique); HERMIER (Marc); THOBOIS (Stéphane)
AF : Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C/Lyon/France (1 aut., 2 aut., 4 aut., 8 aut.); Université de Lyon, Hospices Civils de Lyon, CTRS-IDEE, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie Fonctionnelle et d'Epileptologie/Lyon/France (3 aut.); Centre Hospitalier Valence, Service de Neurologie/Valence/France (5 aut.); Université de Lyon, CERMEP-Imagerie du vivant/69677 Bron/France (6 aut.); Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neuroradiologie/Lyon/France (7 aut.); INSERM U 864/Bron/France (8 aut.)
DT : Publication en série; Courte communication, note brève; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2007; Vol. 22; No. 12; Pp. 1793-1796; Bibl. 10 ref.
LA : Anglais
EA : Malformations of cortical development (MCD) with polymicrogyria and schizencephaly are due to abnormal cortical organization and usually manifest by intractable epilepsy and mental retardation. Epileptical activity is often hard to register and focal dystonia associated with such MCD has previously been described but without any metabolic imaging. We report here a 46-year-old man presenting with late-onset atypical abnormal movements of his left hand associated with right central region MCD. To demonstrate the involvement of an epileptical focus, we performed [18F]FDG-PET and fMRI both before and after a single dose of clobazam and diazepam, respectively. Characteristics of the abnormal hand movements, clinical response to the medication, and the result of the [18F]FDG-PET and fMRI investigations all favor the diagnosis of epilepsia partialis continua. We conclude that the dystonic movement is part of the partial seizure.
CC : 002B17; 002B17C; 002B17F
FD : Système nerveux pathologie; Dystonie; Main; Homme; Malformation
FG : Extrapyramidal syndrome; Mouvement involontaire; Muscle strié pathologie; Trouble neurologique; Encéphale pathologie; Système nerveux central pathologie
ED : Nervous system diseases; Dystonia; Hand; Human; Malformation
EG : Extrapyramidal syndrome; Involuntary movement; Striated muscle disease; Neurological disorder; Cerebral disorder; Central nervous system disease
SD : Sistema nervioso patología; Distonía; Mano; Hombre; Malformación
LO : INIST-20953.354000143464810160
ID : 07-0491129

Links to Exploration step

Pascal:07-0491129

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en" level="a">Epilepsia partialis continua with dystonic hand movement in a patient with a malformation of cortical development</title>
<author>
<name sortKey="Zyss, Julie" sort="Zyss, Julie" uniqKey="Zyss J" first="Julie" last="Zyss">Julie Zyss</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Xie Brustolin, Jing" sort="Xie Brustolin, Jing" uniqKey="Xie Brustolin J" first="Jing" last="Xie-Brustolin">Jing Xie-Brustolin</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Ryvlin, Philippe" sort="Ryvlin, Philippe" uniqKey="Ryvlin P" first="Philippe" last="Ryvlin">Philippe Ryvlin</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Université de Lyon, Hospices Civils de Lyon, CTRS-IDEE, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie Fonctionnelle et d'Epileptologie</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Peysson, Stephane" sort="Peysson, Stephane" uniqKey="Peysson S" first="Stephane" last="Peysson">Stephane Peysson</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Beschet, Albert" sort="Beschet, Albert" uniqKey="Beschet A" first="Albert" last="Beschet">Albert Beschet</name>
<affiliation>
<inist:fA14 i1="03">
<s1>Centre Hospitalier Valence, Service de Neurologie</s1>
<s2>Valence</s2>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Sappey Marinier, Dominique" sort="Sappey Marinier, Dominique" uniqKey="Sappey Marinier D" first="Dominique" last="Sappey-Marinier">Dominique Sappey-Marinier</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Université de Lyon, CERMEP-Imagerie du vivant</s1>
<s2>69677 Bron</s2>
<s3>FRA</s3>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Hermier, Marc" sort="Hermier, Marc" uniqKey="Hermier M" first="Marc" last="Hermier">Marc Hermier</name>
<affiliation>
<inist:fA14 i1="05">
<s1>Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neuroradiologie</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Thobois, Stephane" sort="Thobois, Stephane" uniqKey="Thobois S" first="Stéphane" last="Thobois">Stéphane Thobois</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="06">
<s1>INSERM U 864</s1>
<s2>Bron</s2>
<s3>FRA</s3>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">INIST</idno>
<idno type="inist">07-0491129</idno>
<date when="2007">2007</date>
<idno type="stanalyst">PASCAL 07-0491129 INIST</idno>
<idno type="RBID">Pascal:07-0491129</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">001533</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a">Epilepsia partialis continua with dystonic hand movement in a patient with a malformation of cortical development</title>
<author>
<name sortKey="Zyss, Julie" sort="Zyss, Julie" uniqKey="Zyss J" first="Julie" last="Zyss">Julie Zyss</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Xie Brustolin, Jing" sort="Xie Brustolin, Jing" uniqKey="Xie Brustolin J" first="Jing" last="Xie-Brustolin">Jing Xie-Brustolin</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Ryvlin, Philippe" sort="Ryvlin, Philippe" uniqKey="Ryvlin P" first="Philippe" last="Ryvlin">Philippe Ryvlin</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Université de Lyon, Hospices Civils de Lyon, CTRS-IDEE, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie Fonctionnelle et d'Epileptologie</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Peysson, Stephane" sort="Peysson, Stephane" uniqKey="Peysson S" first="Stephane" last="Peysson">Stephane Peysson</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Beschet, Albert" sort="Beschet, Albert" uniqKey="Beschet A" first="Albert" last="Beschet">Albert Beschet</name>
<affiliation>
<inist:fA14 i1="03">
<s1>Centre Hospitalier Valence, Service de Neurologie</s1>
<s2>Valence</s2>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Sappey Marinier, Dominique" sort="Sappey Marinier, Dominique" uniqKey="Sappey Marinier D" first="Dominique" last="Sappey-Marinier">Dominique Sappey-Marinier</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Université de Lyon, CERMEP-Imagerie du vivant</s1>
<s2>69677 Bron</s2>
<s3>FRA</s3>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Hermier, Marc" sort="Hermier, Marc" uniqKey="Hermier M" first="Marc" last="Hermier">Marc Hermier</name>
<affiliation>
<inist:fA14 i1="05">
<s1>Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neuroradiologie</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Thobois, Stephane" sort="Thobois, Stephane" uniqKey="Thobois S" first="Stéphane" last="Thobois">Stéphane Thobois</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="06">
<s1>INSERM U 864</s1>
<s2>Bron</s2>
<s3>FRA</s3>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint>
<date when="2007">2007</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Dystonia</term>
<term>Hand</term>
<term>Human</term>
<term>Malformation</term>
<term>Nervous system diseases</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Système nerveux pathologie</term>
<term>Dystonie</term>
<term>Main</term>
<term>Homme</term>
<term>Malformation</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Malformations of cortical development (MCD) with polymicrogyria and schizencephaly are due to abnormal cortical organization and usually manifest by intractable epilepsy and mental retardation. Epileptical activity is often hard to register and focal dystonia associated with such MCD has previously been described but without any metabolic imaging. We report here a 46-year-old man presenting with late-onset atypical abnormal movements of his left hand associated with right central region MCD. To demonstrate the involvement of an epileptical focus, we performed [
<sup>18</sup>
F]FDG-PET and fMRI both before and after a single dose of clobazam and diazepam, respectively. Characteristics of the abnormal hand movements, clinical response to the medication, and the result of the [
<sup>18</sup>
F]FDG-PET and fMRI investigations all favor the diagnosis of epilepsia partialis continua. We conclude that the dystonic movement is part of the partial seizure.</div>
</front>
</TEI>
<inist>
<standard h6="B">
<pA>
<fA01 i1="01" i2="1">
<s0>0885-3185</s0>
</fA01>
<fA03 i2="1">
<s0>Mov. disord.</s0>
</fA03>
<fA05>
<s2>22</s2>
</fA05>
<fA06>
<s2>12</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG">
<s1>Epilepsia partialis continua with dystonic hand movement in a patient with a malformation of cortical development</s1>
</fA08>
<fA11 i1="01" i2="1">
<s1>ZYSS (Julie)</s1>
</fA11>
<fA11 i1="02" i2="1">
<s1>XIE-BRUSTOLIN (Jing)</s1>
</fA11>
<fA11 i1="03" i2="1">
<s1>RYVLIN (Philippe)</s1>
</fA11>
<fA11 i1="04" i2="1">
<s1>PEYSSON (Stephane)</s1>
</fA11>
<fA11 i1="05" i2="1">
<s1>BESCHET (Albert)</s1>
</fA11>
<fA11 i1="06" i2="1">
<s1>SAPPEY-MARINIER (Dominique)</s1>
</fA11>
<fA11 i1="07" i2="1">
<s1>HERMIER (Marc)</s1>
</fA11>
<fA11 i1="08" i2="1">
<s1>THOBOIS (Stéphane)</s1>
</fA11>
<fA14 i1="01">
<s1>Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>8 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>Université de Lyon, Hospices Civils de Lyon, CTRS-IDEE, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie Fonctionnelle et d'Epileptologie</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="03">
<s1>Centre Hospitalier Valence, Service de Neurologie</s1>
<s2>Valence</s2>
<s3>FRA</s3>
<sZ>5 aut.</sZ>
</fA14>
<fA14 i1="04">
<s1>Université de Lyon, CERMEP-Imagerie du vivant</s1>
<s2>69677 Bron</s2>
<s3>FRA</s3>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="05">
<s1>Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neuroradiologie</s1>
<s2>Lyon</s2>
<s3>FRA</s3>
<sZ>7 aut.</sZ>
</fA14>
<fA14 i1="06">
<s1>INSERM U 864</s1>
<s2>Bron</s2>
<s3>FRA</s3>
<sZ>8 aut.</sZ>
</fA14>
<fA20>
<s1>1793-1796</s1>
</fA20>
<fA21>
<s1>2007</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>20953</s2>
<s5>354000143464810160</s5>
</fA43>
<fA44>
<s0>0000</s0>
<s1>© 2007 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>10 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>07-0491129</s0>
</fA47>
<fA60>
<s1>P</s1>
<s3>CC</s3>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Movement disorders</s0>
</fA64>
<fA66 i1="01">
<s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>Malformations of cortical development (MCD) with polymicrogyria and schizencephaly are due to abnormal cortical organization and usually manifest by intractable epilepsy and mental retardation. Epileptical activity is often hard to register and focal dystonia associated with such MCD has previously been described but without any metabolic imaging. We report here a 46-year-old man presenting with late-onset atypical abnormal movements of his left hand associated with right central region MCD. To demonstrate the involvement of an epileptical focus, we performed [
<sup>18</sup>
F]FDG-PET and fMRI both before and after a single dose of clobazam and diazepam, respectively. Characteristics of the abnormal hand movements, clinical response to the medication, and the result of the [
<sup>18</sup>
F]FDG-PET and fMRI investigations all favor the diagnosis of epilepsia partialis continua. We conclude that the dystonic movement is part of the partial seizure.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002B17</s0>
</fC02>
<fC02 i1="02" i2="X">
<s0>002B17C</s0>
</fC02>
<fC02 i1="03" i2="X">
<s0>002B17F</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Système nerveux pathologie</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Nervous system diseases</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Sistema nervioso patología</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Dystonie</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Dystonia</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Distonía</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Main</s0>
<s5>09</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Hand</s0>
<s5>09</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Mano</s0>
<s5>09</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Homme</s0>
<s5>10</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Human</s0>
<s5>10</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Hombre</s0>
<s5>10</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Malformation</s0>
<s5>11</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Malformation</s0>
<s5>11</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Malformación</s0>
<s5>11</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Extrapyramidal syndrome</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Extrapyramidal syndrome</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Extrapiramidal síndrome</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Mouvement involontaire</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Involuntary movement</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Movimiento involuntario</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Muscle strié pathologie</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Striated muscle disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Músculo estriado patología</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Trouble neurologique</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Neurological disorder</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Trastorno neurológico</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Encéphale pathologie</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Cerebral disorder</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Encéfalo patología</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Système nerveux central pathologie</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Central nervous system disease</s0>
<s5>42</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Sistema nervosio central patología</s0>
<s5>42</s5>
</fC07>
<fN21>
<s1>323</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 07-0491129 INIST</NO>
<ET>Epilepsia partialis continua with dystonic hand movement in a patient with a malformation of cortical development</ET>
<AU>ZYSS (Julie); XIE-BRUSTOLIN (Jing); RYVLIN (Philippe); PEYSSON (Stephane); BESCHET (Albert); SAPPEY-MARINIER (Dominique); HERMIER (Marc); THOBOIS (Stéphane)</AU>
<AF>Université de Lyon, Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie C/Lyon/France (1 aut., 2 aut., 4 aut., 8 aut.); Université de Lyon, Hospices Civils de Lyon, CTRS-IDEE, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neurologie Fonctionnelle et d'Epileptologie/Lyon/France (3 aut.); Centre Hospitalier Valence, Service de Neurologie/Valence/France (5 aut.); Université de Lyon, CERMEP-Imagerie du vivant/69677 Bron/France (6 aut.); Hospices Civils de Lyon, Hôpital Neurologique et Neurochirurgical Pierre Wertheimer, Service de Neuroradiologie/Lyon/France (7 aut.); INSERM U 864/Bron/France (8 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2007; Vol. 22; No. 12; Pp. 1793-1796; Bibl. 10 ref.</SO>
<LA>Anglais</LA>
<EA>Malformations of cortical development (MCD) with polymicrogyria and schizencephaly are due to abnormal cortical organization and usually manifest by intractable epilepsy and mental retardation. Epileptical activity is often hard to register and focal dystonia associated with such MCD has previously been described but without any metabolic imaging. We report here a 46-year-old man presenting with late-onset atypical abnormal movements of his left hand associated with right central region MCD. To demonstrate the involvement of an epileptical focus, we performed [
<sup>18</sup>
F]FDG-PET and fMRI both before and after a single dose of clobazam and diazepam, respectively. Characteristics of the abnormal hand movements, clinical response to the medication, and the result of the [
<sup>18</sup>
F]FDG-PET and fMRI investigations all favor the diagnosis of epilepsia partialis continua. We conclude that the dystonic movement is part of the partial seizure.</EA>
<CC>002B17; 002B17C; 002B17F</CC>
<FD>Système nerveux pathologie; Dystonie; Main; Homme; Malformation</FD>
<FG>Extrapyramidal syndrome; Mouvement involontaire; Muscle strié pathologie; Trouble neurologique; Encéphale pathologie; Système nerveux central pathologie</FG>
<ED>Nervous system diseases; Dystonia; Hand; Human; Malformation</ED>
<EG>Extrapyramidal syndrome; Involuntary movement; Striated muscle disease; Neurological disorder; Cerebral disorder; Central nervous system disease</EG>
<SD>Sistema nervioso patología; Distonía; Mano; Hombre; Malformación</SD>
<LO>INIST-20953.354000143464810160</LO>
<ID>07-0491129</ID>
</server>
</inist>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/PascalFrancis/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001533 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Corpus/biblio.hfd -nk 001533 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    PascalFrancis
   |étape=   Corpus
   |type=    RBID
   |clé=     Pascal:07-0491129
   |texte=   Epilepsia partialis continua with dystonic hand movement in a patient with a malformation of cortical development
}}

Wicri

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024