Camptocormia in Parkinson's disease mimicked by focal myositis of the paraspinal muscles.
Identifieur interne : 003B72 ( PubMed/Checkpoint ); précédent : 003B71; suivant : 003B73Camptocormia in Parkinson's disease mimicked by focal myositis of the paraspinal muscles.
Auteurs : Silke Wunderlich [Allemagne] ; Ilona Csoti ; Karlheinz Reiners ; Thomas Günthner-Lengsfeld ; Christiane Schneider ; Georg Becker ; Markus NaumannSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2002.
English descriptors
- KwdEn :
- Anti-Inflammatory Agents (therapeutic use), Back, Biopsy, Needle, Creatine Kinase (blood), Diagnosis, Differential, Humans, Kyphosis (diagnosis), Kyphosis (etiology), Magnetic Resonance Imaging, Male, Methylprednisolone (therapeutic use), Middle Aged, Myositis (complications), Myositis (diagnosis), Myositis (drug therapy), Parkinson Disease (complications), Posture, Treatment Outcome.
- MESH :
- chemical , blood : Creatine Kinase.
- chemical , therapeutic use : Anti-Inflammatory Agents, Methylprednisolone.
- complications : Myositis, Parkinson Disease.
- diagnosis : Kyphosis, Myositis.
- drug therapy : Myositis.
- etiology : Kyphosis.
- Back, Biopsy, Needle, Diagnosis, Differential, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Posture, Treatment Outcome.
Abstract
We report on a 63-year-old man with idiopathic Parkinson's disease who developed kyphosis and a severe forward flexion of the thoracolumbar spine. A typical feature was an increase during walking or standing and it completely disappeared in the supine position, mimicking the clinical phenomenon of camptocormia (bent spine). In addition to the abnormal posture, a weakness of the erector spinal muscles, local pain, reddening, and elevated temperature of the paraspinal muscles were evident. Creatine kinase was initially elevated, electromyography showed spontaneous activity and a myopathic pattern. Magnetic resonance imaging and bioptic examinations revealed a focal myositis of the paraspinal muscles. This case indicates that camptocormia can be mimicked by focal myositis of paraspinal muscles and must be included in the differential diagnosis, especially when additional symptoms as inflammatory signs or weakness are present.
DOI: 10.1002/mds.10110
PubMed: 12112214
Affiliations:
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uniqKey="Reiners K" first="Karlheinz" last="Reiners">Karlheinz Reiners</name></author><author><name sortKey="Gunthner Lengsfeld, Thomas" sort="Gunthner Lengsfeld, Thomas" uniqKey="Gunthner Lengsfeld T" first="Thomas" last="Günthner-Lengsfeld">Thomas Günthner-Lengsfeld</name></author><author><name sortKey="Schneider, Christiane" sort="Schneider, Christiane" uniqKey="Schneider C" first="Christiane" last="Schneider">Christiane Schneider</name></author><author><name sortKey="Becker, Georg" sort="Becker, Georg" uniqKey="Becker G" first="Georg" last="Becker">Georg Becker</name></author><author><name sortKey="Naumann, Markus" sort="Naumann, Markus" uniqKey="Naumann M" first="Markus" last="Naumann">Markus Naumann</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2002">2002</date><idno type="RBID">pubmed:12112214</idno><idno type="pmid">12112214</idno><idno type="doi">10.1002/mds.10110</idno><idno type="wicri:Area/PubMed/Corpus">003A44</idno><idno type="wicri:Area/PubMed/Curation">003A44</idno><idno type="wicri:Area/PubMed/Checkpoint">003B72</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Camptocormia in Parkinson's disease mimicked by focal myositis of the paraspinal muscles.</title><author><name sortKey="Wunderlich, Silke" sort="Wunderlich, Silke" uniqKey="Wunderlich S" first="Silke" last="Wunderlich">Silke Wunderlich</name><affiliation wicri:level="3"><nlm:affiliation>Department of Neurology, Julius-Maximilian-Universität, Würzburg, Germany.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Department of Neurology, Julius-Maximilian-Universität, Würzburg</wicri:regionArea><placeName><region type="land" nuts="1">Bavière</region><region type="district" nuts="2">District de Basse-Franconie</region><settlement type="city">Wurtzbourg</settlement></placeName></affiliation></author><author><name sortKey="Csoti, Ilona" sort="Csoti, Ilona" uniqKey="Csoti I" first="Ilona" last="Csoti">Ilona Csoti</name></author><author><name sortKey="Reiners, Karlheinz" sort="Reiners, Karlheinz" uniqKey="Reiners K" first="Karlheinz" last="Reiners">Karlheinz Reiners</name></author><author><name sortKey="Gunthner Lengsfeld, Thomas" sort="Gunthner Lengsfeld, Thomas" uniqKey="Gunthner Lengsfeld T" first="Thomas" last="Günthner-Lengsfeld">Thomas Günthner-Lengsfeld</name></author><author><name sortKey="Schneider, Christiane" sort="Schneider, Christiane" uniqKey="Schneider C" first="Christiane" last="Schneider">Christiane Schneider</name></author><author><name sortKey="Becker, Georg" sort="Becker, Georg" uniqKey="Becker G" first="Georg" last="Becker">Georg Becker</name></author><author><name sortKey="Naumann, Markus" sort="Naumann, Markus" uniqKey="Naumann M" first="Markus" last="Naumann">Markus Naumann</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="2002" type="published">2002</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Anti-Inflammatory Agents (therapeutic use)</term><term>Back</term><term>Biopsy, Needle</term><term>Creatine Kinase (blood)</term><term>Diagnosis, Differential</term><term>Humans</term><term>Kyphosis (diagnosis)</term><term>Kyphosis (etiology)</term><term>Magnetic Resonance Imaging</term><term>Male</term><term>Methylprednisolone (therapeutic use)</term><term>Middle Aged</term><term>Myositis (complications)</term><term>Myositis (diagnosis)</term><term>Myositis (drug therapy)</term><term>Parkinson Disease (complications)</term><term>Posture</term><term>Treatment Outcome</term></keywords><keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en"><term>Creatine Kinase</term></keywords><keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Anti-Inflammatory Agents</term><term>Methylprednisolone</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Myositis</term><term>Parkinson Disease</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Kyphosis</term><term>Myositis</term></keywords><keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Myositis</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Kyphosis</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Back</term><term>Biopsy, Needle</term><term>Diagnosis, Differential</term><term>Humans</term><term>Magnetic Resonance Imaging</term><term>Male</term><term>Middle Aged</term><term>Posture</term><term>Treatment Outcome</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We report on a 63-year-old man with idiopathic Parkinson's disease who developed kyphosis and a severe forward flexion of the thoracolumbar spine. A typical feature was an increase during walking or standing and it completely disappeared in the supine position, mimicking the clinical phenomenon of camptocormia (bent spine). In addition to the abnormal posture, a weakness of the erector spinal muscles, local pain, reddening, and elevated temperature of the paraspinal muscles were evident. Creatine kinase was initially elevated, electromyography showed spontaneous activity and a myopathic pattern. Magnetic resonance imaging and bioptic examinations revealed a focal myositis of the paraspinal muscles. This case indicates that camptocormia can be mimicked by focal myositis of paraspinal muscles and must be included in the differential diagnosis, especially when additional symptoms as inflammatory signs or weakness are present.</div></front></TEI><pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">12112214</PMID><DateCreated><Year>2002</Year><Month>07</Month><Day>11</Day></DateCreated><DateCompleted><Year>2002</Year><Month>09</Month><Day>16</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0885-3185</ISSN><JournalIssue CitedMedium="Print"><Volume>17</Volume><Issue>3</Issue><PubDate><Year>2002</Year><Month>May</Month></PubDate></JournalIssue><Title>Movement disorders : official journal of the Movement Disorder Society</Title><ISOAbbreviation>Mov. Disord.</ISOAbbreviation></Journal><ArticleTitle>Camptocormia in Parkinson's disease mimicked by focal myositis of the paraspinal muscles.</ArticleTitle><Pagination><MedlinePgn>598-600</MedlinePgn></Pagination><Abstract><AbstractText>We report on a 63-year-old man with idiopathic Parkinson's disease who developed kyphosis and a severe forward flexion of the thoracolumbar spine. A typical feature was an increase during walking or standing and it completely disappeared in the supine position, mimicking the clinical phenomenon of camptocormia (bent spine). In addition to the abnormal posture, a weakness of the erector spinal muscles, local pain, reddening, and elevated temperature of the paraspinal muscles were evident. Creatine kinase was initially elevated, electromyography showed spontaneous activity and a myopathic pattern. Magnetic resonance imaging and bioptic examinations revealed a focal myositis of the paraspinal muscles. This case indicates that camptocormia can be mimicked by focal myositis of paraspinal muscles and must be included in the differential diagnosis, especially when additional symptoms as inflammatory signs or weakness are present.</AbstractText><CopyrightInformation>Copyright 2002 Movement Disorder Society.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Wunderlich</LastName><ForeName>Silke</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Department of Neurology, Julius-Maximilian-Universität, Würzburg, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Csoti</LastName><ForeName>Ilona</ForeName><Initials>I</Initials></Author><Author ValidYN="Y"><LastName>Reiners</LastName><ForeName>Karlheinz</ForeName><Initials>K</Initials></Author><Author ValidYN="Y"><LastName>Günthner-Lengsfeld</LastName><ForeName>Thomas</ForeName><Initials>T</Initials></Author><Author ValidYN="Y"><LastName>Schneider</LastName><ForeName>Christiane</ForeName><Initials>C</Initials></Author><Author ValidYN="Y"><LastName>Becker</LastName><ForeName>Georg</ForeName><Initials>G</Initials></Author><Author ValidYN="Y"><LastName>Naumann</LastName><ForeName>Markus</ForeName><Initials>M</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Mov Disord</MedlineTA><NlmUniqueID>8610688</NlmUniqueID><ISSNLinking>0885-3185</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000893">Anti-Inflammatory Agents</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 2.7.3.2</RegistryNumber><NameOfSubstance UI="D003402">Creatine 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UI="D006801">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D007738">Kyphosis</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000175">diagnosis</QualifierName><QualifierName MajorTopicYN="N" UI="Q000209">etiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D008279">Magnetic Resonance Imaging</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D008775">Methylprednisolone</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000627">therapeutic use</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D009220">Myositis</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000150">complications</QualifierName><QualifierName MajorTopicYN="Y" UI="Q000175">diagnosis</QualifierName><QualifierName MajorTopicYN="N" UI="Q000188">drug therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D010300">Parkinson Disease</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000150">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D011187">Posture</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D016896">Treatment Outcome</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2002</Year><Month>7</Month><Day>12</Day><Hour>10</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2002</Year><Month>9</Month><Day>17</Day><Hour>10</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2002</Year><Month>7</Month><Day>12</Day><Hour>10</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">12112214</ArticleId><ArticleId IdType="doi">10.1002/mds.10110</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Allemagne</li></country><region><li>Bavière</li><li>District de Basse-Franconie</li></region><settlement><li>Wurtzbourg</li></settlement></list><tree><noCountry><name sortKey="Becker, Georg" sort="Becker, Georg" uniqKey="Becker G" first="Georg" last="Becker">Georg Becker</name><name sortKey="Csoti, Ilona" sort="Csoti, Ilona" uniqKey="Csoti I" first="Ilona" last="Csoti">Ilona Csoti</name><name sortKey="Gunthner Lengsfeld, Thomas" sort="Gunthner Lengsfeld, Thomas" uniqKey="Gunthner Lengsfeld T" first="Thomas" last="Günthner-Lengsfeld">Thomas Günthner-Lengsfeld</name><name sortKey="Naumann, Markus" sort="Naumann, Markus" uniqKey="Naumann M" first="Markus" last="Naumann">Markus Naumann</name><name sortKey="Reiners, Karlheinz" sort="Reiners, Karlheinz" uniqKey="Reiners K" first="Karlheinz" last="Reiners">Karlheinz Reiners</name><name sortKey="Schneider, Christiane" sort="Schneider, Christiane" uniqKey="Schneider C" first="Christiane" last="Schneider">Christiane Schneider</name></noCountry><country name="Allemagne"><region name="Bavière"><name sortKey="Wunderlich, Silke" sort="Wunderlich, Silke" uniqKey="Wunderlich S" first="Silke" last="Wunderlich">Silke Wunderlich</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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