Paraneoplastic syndromes of the spinal cord, nerve, and muscle
Identifieur interne : 006B58 ( Istex/Corpus ); précédent : 006B57; suivant : 006B59Paraneoplastic syndromes of the spinal cord, nerve, and muscle
Auteurs : Stacy A. Rudnicki ; Josep DalmauSource :
- Muscle & Nerve [ 0148-639X ] ; 2000-12.
Abstract
Cancer can affect the peripheral nervous system by non‐metastatic, sometimes immune‐mediated mechanisms. Recognition of these paraneoplastic syndromes is important because it can lead to the detection of the tumor, and also helps to avoid unnecessary studies to determine the cause of the neurologic symptoms in patients with cancer. Many paraneoplastic syndromes of the peripheral nervous system are not associated with serum antibodies that serve as markers of paraneoplasia. For this group of disorders the diagnosis depends on the clinician's index of suspicion and conventional electrophysiologic and laboratory tests. Treatment of the tumor, immunotherapy, or both may improve some of these syndromes. This review focuses on paraneoplastic syndromes of the spinal cord, peripheral nerve, and muscle. © 2000 John Wiley & Sons, Inc. Muscle Nerve 23: 1800–1818, 2000
Url:
DOI: 10.1002/1097-4598(200012)23:12<1800::AID-MUS3>3.0.CO;2-X
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ISTEX:E5461FD240D73CC7BD0106F6F0D44B588C725C74Le document en format XML
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xml:id="kwd2">myopathy</keyword><keyword xml:id="kwd3">neuropathy</keyword><keyword xml:id="kwd4">paraneoplastic</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>Cancer can affect the peripheral nervous system by non‐metastatic, sometimes immune‐mediated mechanisms. Recognition of these paraneoplastic syndromes is important because it can lead to the detection of the tumor, and also helps to avoid unnecessary studies to determine the cause of the neurologic symptoms in patients with cancer. Many paraneoplastic syndromes of the peripheral nervous system are not associated with serum antibodies that serve as markers of paraneoplasia. For this group of disorders the diagnosis depends on the clinician's index of suspicion and conventional electrophysiologic and laboratory tests. Treatment of the tumor, immunotherapy, or both may improve some of these syndromes. This review focuses on paraneoplastic syndromes of the spinal cord, peripheral nerve, and muscle. © 2000 John Wiley & Sons, Inc. Muscle Nerve 23: 1800–1818, 2000</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Paraneoplastic syndromes of the spinal cord, nerve, and muscle</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Paraneoplastic Syndromes</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Paraneoplastic syndromes of the spinal cord, nerve, and muscle</title></titleInfo><name type="personal"><namePart type="given">Stacy A.</namePart><namePart type="family">Rudnicki</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, University of Arkansas for Medical Sciences, 4301 West Markham, Slot 500, Little Rock, Arkansas 72205, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Josep</namePart><namePart type="family">Dalmau</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Neurology, University of Arkansas for Medical Sciences, 4301 West Markham, Slot 500, Little Rock, Arkansas 72205, USA</affiliation><affiliation>Arkansas Cancer Research Center, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA</affiliation><affiliation>Department of Neurology, University of Arkansas for Medical Sciences, 4301 West Markham, Slot 500, Little Rock, Arkansas 72205, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="review-article" displayLabel="reviewArticle"></genre><originInfo><publisher>John Wiley & Sons, Inc.</publisher><place><placeTerm type="text">New York</placeTerm></place><dateIssued encoding="w3cdtf">2000-12</dateIssued><dateValid encoding="w3cdtf">2000-06-13</dateValid><copyrightDate encoding="w3cdtf">2000</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">2</extent><extent unit="tables">2</extent><extent unit="references">259</extent><extent unit="words">12495</extent></physicalDescription><abstract lang="en">Cancer can affect the peripheral nervous system by non‐metastatic, sometimes immune‐mediated mechanisms. Recognition of these paraneoplastic syndromes is important because it can lead to the detection of the tumor, and also helps to avoid unnecessary studies to determine the cause of the neurologic symptoms in patients with cancer. Many paraneoplastic syndromes of the peripheral nervous system are not associated with serum antibodies that serve as markers of paraneoplasia. For this group of disorders the diagnosis depends on the clinician's index of suspicion and conventional electrophysiologic and laboratory tests. Treatment of the tumor, immunotherapy, or both may improve some of these syndromes. This review focuses on paraneoplastic syndromes of the spinal cord, peripheral nerve, and muscle. © 2000 John Wiley & Sons, Inc. Muscle Nerve 23: 1800–1818, 2000</abstract><subject lang="en"><genre>keywords</genre><topic>myelopathy</topic><topic>myopathy</topic><topic>neuropathy</topic><topic>paraneoplastic</topic></subject><relatedItem type="host"><titleInfo><title>Muscle & Nerve</title><subTitle>Official Journal of the American Association of Electrodiagnostic Medicine</subTitle></titleInfo><titleInfo type="abbreviated"><title>Muscle Nerve</title></titleInfo><genre type="journal">journal</genre><subject><genre>article-category</genre><topic>Invited Review</topic></subject><identifier type="ISSN">0148-639X</identifier><identifier type="eISSN">1097-4598</identifier><identifier type="DOI">10.1002/(ISSN)1097-4598</identifier><identifier type="PublisherID">MUS</identifier><part><date>2000</date><detail type="volume"><caption>vol.</caption><number>23</number></detail><detail type="issue"><caption>no.</caption><number>12</number></detail><extent unit="pages"><start>1800</start><end>1818</end><total>19</total></extent></part></relatedItem><identifier type="istex">E5461FD240D73CC7BD0106F6F0D44B588C725C74</identifier><identifier type="DOI">10.1002/1097-4598(200012)23:12<1800::AID-MUS3>3.0.CO;2-X</identifier><identifier type="ArticleID">MUS3</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2000 John Wiley & Sons, Inc.</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>John Wiley & Sons, Inc.</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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