Meige syndrome: Neuropathology of a case
Identifieur interne : 009909 ( Main/Merge ); précédent : 009908; suivant : 009910Meige syndrome: Neuropathology of a case
Auteurs : J. Kulisevsky [Espagne] ; M. J. Marti [Espagne] ; I. Ferrer [Espagne] ; Tolosa [Espagne]Source :
- Movement Disorders [ 0885-3185 ] ; 1988.
English descriptors
- KwdEn :
- MESH :
- etiology : Meige Syndrome.
- pathology : Basal Ganglia Diseases, Brain Stem, Meige Syndrome.
- physiopathology : Meige Syndrome.
- Aged, Humans, Male, Movement, Muscle Contraction.
Abstract
Primary Meige syndrome is a form of cranial dystonia of unknown cause. Only three postmortem studies have been reported, and the results of these studies have not been consistent. We have examined the brain of a 72‐year‐old man with typical primary Meige syndrome and found mild to moderate cell loss in the zona compacta of the substanita nigra, locus ceuleus, midbrain tectum, and dentate nucleus of the cerebellum. Also frequent lewy bodies were present in pigmented nuclei of the brainstem. No abnormalities were detected elsewhere. These pathological findings support the notion that brainstem pathology is important in the pathophysiology of cranial dystonia.
Url:
DOI: 10.1002/mds.870030209
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Ferrer</name><affiliation wicri:level="3"><country xml:lang="fr">Espagne</country><wicri:regionArea>Department of Pathology. Hospital de la Sta. Creu iS.Pau, Barcelona</wicri:regionArea><placeName><settlement type="city">Barcelone</settlement><region nuts="2" type="region">Catalogne</region></placeName></affiliation></author><author><name sortKey="Tolosa" sort="Tolosa" uniqKey="Tolosa" last="Tolosa">Tolosa</name><affiliation wicri:level="3"><country xml:lang="fr">Espagne</country><wicri:regionArea>Neurology Service, Hospital Clinic i Provincial, Faculty of Medicine, Barcelona</wicri:regionArea><placeName><settlement type="city">Barcelone</settlement><region nuts="2" type="region">Catalogne</region></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="sub">Official Journal of the Movement Disorder Society</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1988">1988</date><biblScope unit="vol">3</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="170">170</biblScope><biblScope unit="page" to="175">175</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">040C60953C1AE3B2A58BB8215A542C5C0FB34E89</idno><idno type="DOI">10.1002/mds.870030209</idno><idno type="ArticleID">MDS870030209</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Basal Ganglia Diseases (pathology)</term><term>Brain Stem (pathology)</term><term>Brainstem pathology</term><term>Cranial dystonia</term><term>Humans</term><term>Male</term><term>Meige Syndrome</term><term>Meige Syndrome (etiology)</term><term>Meige Syndrome (pathology)</term><term>Meige Syndrome (physiopathology)</term><term>Movement</term><term>Muscle Contraction</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Meige Syndrome</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Basal Ganglia Diseases</term><term>Brain Stem</term><term>Meige Syndrome</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Meige Syndrome</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Humans</term><term>Male</term><term>Movement</term><term>Muscle Contraction</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Primary Meige syndrome is a form of cranial dystonia of unknown cause. Only three postmortem studies have been reported, and the results of these studies have not been consistent. We have examined the brain of a 72‐year‐old man with typical primary Meige syndrome and found mild to moderate cell loss in the zona compacta of the substanita nigra, locus ceuleus, midbrain tectum, and dentate nucleus of the cerebellum. Also frequent lewy bodies were present in pigmented nuclei of the brainstem. No abnormalities were detected elsewhere. These pathological findings support the notion that brainstem pathology is important in the pathophysiology of cranial dystonia.</div></front></TEI><double doi="10.1002/mds.870030209"><ISTEX><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Meige syndrome: Neuropathology of a case</title><author><name sortKey="Kulisevsky, J" sort="Kulisevsky, J" uniqKey="Kulisevsky J" first="J." last="Kulisevsky">J. 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Ferrer</name></author><author><name sortKey="Tolosa" sort="Tolosa" uniqKey="Tolosa" last="Tolosa">Tolosa</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:040C60953C1AE3B2A58BB8215A542C5C0FB34E89</idno><date when="1988" year="1988">1988</date><idno type="doi">10.1002/mds.870030209</idno><idno type="url">https://api.istex.fr/document/040C60953C1AE3B2A58BB8215A542C5C0FB34E89/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">003633</idno><idno type="wicri:Area/Istex/Curation">003633</idno><idno type="wicri:Area/Istex/Checkpoint">004540</idno><idno type="wicri:doubleKey">0885-3185:1988:Kulisevsky J:meige:syndrome:neuropathology</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Meige syndrome: Neuropathology of a case</title><author><name sortKey="Kulisevsky, J" sort="Kulisevsky, J" uniqKey="Kulisevsky J" first="J." last="Kulisevsky">J. Kulisevsky</name><affiliation wicri:level="3"><country xml:lang="fr">Espagne</country><wicri:regionArea>Neurology Service, Hospital Clinic i Provincial, Faculty of Medicine, Barcelona</wicri:regionArea><placeName><settlement type="city">Barcelone</settlement><region nuts="2" type="region">Catalogne</region></placeName></affiliation></author><author><name sortKey="Marti, M J" sort="Marti, M J" uniqKey="Marti M" first="M. J." last="Marti">M. J. Marti</name><affiliation wicri:level="3"><country xml:lang="fr">Espagne</country><wicri:regionArea>Neurology Service, Hospital Clinic i Provincial, Faculty of Medicine, Barcelona</wicri:regionArea><placeName><settlement type="city">Barcelone</settlement><region nuts="2" type="region">Catalogne</region></placeName></affiliation></author><author><name sortKey="Ferrer, I" sort="Ferrer, I" uniqKey="Ferrer I" first="I." last="Ferrer">I. Ferrer</name><affiliation wicri:level="3"><country xml:lang="fr">Espagne</country><wicri:regionArea>Department of Pathology. Hospital de la Sta. Creu iS.Pau, Barcelona</wicri:regionArea><placeName><settlement type="city">Barcelone</settlement><region nuts="2" type="region">Catalogne</region></placeName></affiliation></author><author><name sortKey="Tolosa" sort="Tolosa" uniqKey="Tolosa" last="Tolosa">Tolosa</name><affiliation wicri:level="3"><country xml:lang="fr">Espagne</country><wicri:regionArea>Neurology Service, Hospital Clinic i Provincial, Faculty of Medicine, Barcelona</wicri:regionArea><placeName><settlement type="city">Barcelone</settlement><region nuts="2" type="region">Catalogne</region></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="sub">Official Journal of the Movement Disorder Society</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1988">1988</date><biblScope unit="vol">3</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="170">170</biblScope><biblScope unit="page" to="175">175</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">040C60953C1AE3B2A58BB8215A542C5C0FB34E89</idno><idno type="DOI">10.1002/mds.870030209</idno><idno type="ArticleID">MDS870030209</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Brainstem pathology</term><term>Cranial dystonia</term><term>Meige Syndrome</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Primary Meige syndrome is a form of cranial dystonia of unknown cause. Only three postmortem studies have been reported, and the results of these studies have not been consistent. We have examined the brain of a 72‐year‐old man with typical primary Meige syndrome and found mild to moderate cell loss in the zona compacta of the substanita nigra, locus ceuleus, midbrain tectum, and dentate nucleus of the cerebellum. Also frequent lewy bodies were present in pigmented nuclei of the brainstem. No abnormalities were detected elsewhere. These pathological findings support the notion that brainstem pathology is important in the pathophysiology of cranial dystonia.</div></front></TEI></ISTEX><PubMed><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Meige syndrome: neuropathology of a case.</title><author><name sortKey="Kulisevsky, J" sort="Kulisevsky, J" uniqKey="Kulisevsky J" first="J" last="Kulisevsky">J. Kulisevsky</name><affiliation wicri:level="3"><nlm:affiliation>Neurology Service, Hospital Clinic i Provincial, Faculty of Medicine, Barcelona, Spain.</nlm:affiliation><country xml:lang="fr">Espagne</country><wicri:regionArea>Neurology Service, Hospital Clinic i Provincial, Faculty of Medicine, Barcelona</wicri:regionArea><placeName><settlement type="city">Barcelone</settlement><region nuts="2" type="region">Catalogne</region></placeName></affiliation></author><author><name sortKey="Marti, M J" sort="Marti, M J" uniqKey="Marti M" first="M J" last="Marti">M J Marti</name></author><author><name sortKey="Ferrer, I" sort="Ferrer, I" uniqKey="Ferrer I" first="I" last="Ferrer">I. Ferrer</name></author><author><name sortKey="Tolosa, E" sort="Tolosa, E" uniqKey="Tolosa E" first="E" last="Tolosa">E. Tolosa</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="1988">1988</date><idno type="RBID">pubmed:3221903</idno><idno type="pmid">3221903</idno><idno type="doi">10.1002/mds.870030209</idno><idno type="wicri:Area/PubMed/Corpus">005011</idno><idno type="wicri:Area/PubMed/Curation">005011</idno><idno type="wicri:Area/PubMed/Checkpoint">005029</idno><idno type="wicri:Area/Ncbi/Merge">004620</idno><idno type="wicri:Area/Ncbi/Curation">004620</idno><idno type="wicri:Area/Ncbi/Checkpoint">004620</idno><idno type="wicri:doubleKey">0885-3185:1988:Kulisevsky J:meige:syndrome:neuropathology</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Meige syndrome: neuropathology of a case.</title><author><name sortKey="Kulisevsky, J" sort="Kulisevsky, J" uniqKey="Kulisevsky J" first="J" last="Kulisevsky">J. Kulisevsky</name><affiliation wicri:level="3"><nlm:affiliation>Neurology Service, Hospital Clinic i Provincial, Faculty of Medicine, Barcelona, Spain.</nlm:affiliation><country xml:lang="fr">Espagne</country><wicri:regionArea>Neurology Service, Hospital Clinic i Provincial, Faculty of Medicine, Barcelona</wicri:regionArea><placeName><settlement type="city">Barcelone</settlement><region nuts="2" type="region">Catalogne</region></placeName></affiliation></author><author><name sortKey="Marti, M J" sort="Marti, M J" uniqKey="Marti M" first="M J" last="Marti">M J Marti</name></author><author><name sortKey="Ferrer, I" sort="Ferrer, I" uniqKey="Ferrer I" first="I" last="Ferrer">I. Ferrer</name></author><author><name sortKey="Tolosa, E" sort="Tolosa, E" uniqKey="Tolosa E" first="E" last="Tolosa">E. Tolosa</name></author></analytic><series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title><idno type="ISSN">0885-3185</idno><imprint><date when="1988" type="published">1988</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Basal Ganglia Diseases (pathology)</term><term>Brain Stem (pathology)</term><term>Humans</term><term>Male</term><term>Meige Syndrome (etiology)</term><term>Meige Syndrome (pathology)</term><term>Meige Syndrome (physiopathology)</term><term>Movement</term><term>Muscle Contraction</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Meige Syndrome</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Basal Ganglia Diseases</term><term>Brain Stem</term><term>Meige Syndrome</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Meige Syndrome</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Humans</term><term>Male</term><term>Movement</term><term>Muscle Contraction</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Primary Meige syndrome is a form of cranial dystonia of unknown cause. Only three postmortem studies have been reported, and the results of these studies have not been consistent. We have examined the brain of a 72-year-old man with typical primary Meige syndrome and found mild to moderate cell loss in the zona compacta of the substantia nigra, locus ceruleus, midbrain tectum, and dentate nucleus of the cerebellum. Also frequent Lewy bodies were present in pigmented nuclei of the brainstem. No abnormalities were detected elsewhere. These pathological findings support the notion that brainstem pathology is important in the pathophysiology of cranial dystonia.</div></front></TEI></PubMed></double></record>Pour manipuler ce document sous Unix (Dilib)
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