Diagnosis and Management of Acute Myelopathies
BACKGROUND:Acute myelopathies represent a heterogeneous group of disorders with distinct etiologies, clinical and radiologic features, and prognoses. Transverse myelitis (TM) is a prototype member of this group in which an immune-mediated process causes neural injury to the spinal cord, resulting in...
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Veröffentlicht in: | The Neurologist (Baltimore, Md.) Md.), 2005-01, Vol.11 (1), p.2-18 |
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creator | Kaplin, Adam I. Krishnan, Chitra Deshpande, Deepa M. Pardo, Carlos A. Kerr, Douglas A. |
description | BACKGROUND:Acute myelopathies represent a heterogeneous group of disorders with distinct etiologies, clinical and radiologic features, and prognoses. Transverse myelitis (TM) is a prototype member of this group in which an immune-mediated process causes neural injury to the spinal cord, resulting in varying degrees of weakness, sensory alterations, and autonomic dysfunction. TM may exist as part of a multifocal CNS disease (eg, MS), multisystemic disease (eg, systemic lupus erythematosus), or as an isolated, idiopathic entity.
REVIEW SUMMARY:In this article, we summarize recent classification and diagnostic schemes, which provide a framework for the diagnosis and management of patients with acute myelopathy. Additionally, we review the state of current knowledge about the epidemiology, natural history, immunopathogenesis, and treatment strategies for patients with TM.
CONCLUSIONS:Our understanding of the classification, diagnosis, pathogenesis, and treatment of TM has recently begun to expand dramatically. With more rigorous criteria applied to distinguish acute myelopathies and with an emerging understanding of immunopathogenic events that underlie TM, it may now be possible to effectively initiate treatments in many of these disorders. Through the investigation of TM, we are also gaining a broader appreciation of the mechanisms that lead to autoimmune neurologic diseases in general. |
doi_str_mv | 10.1097/01.nrl.0000149975.39201.0b |
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REVIEW SUMMARY:In this article, we summarize recent classification and diagnostic schemes, which provide a framework for the diagnosis and management of patients with acute myelopathy. Additionally, we review the state of current knowledge about the epidemiology, natural history, immunopathogenesis, and treatment strategies for patients with TM.
CONCLUSIONS:Our understanding of the classification, diagnosis, pathogenesis, and treatment of TM has recently begun to expand dramatically. With more rigorous criteria applied to distinguish acute myelopathies and with an emerging understanding of immunopathogenic events that underlie TM, it may now be possible to effectively initiate treatments in many of these disorders. Through the investigation of TM, we are also gaining a broader appreciation of the mechanisms that lead to autoimmune neurologic diseases in general.</description><identifier>ISSN: 1074-7931</identifier><identifier>EISSN: 2331-2637</identifier><identifier>DOI: 10.1097/01.nrl.0000149975.39201.0b</identifier><identifier>PMID: 15631640</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins, Inc</publisher><subject>Acute Disease ; Decision Trees ; Diagnosis, Differential ; Humans ; Myelitis, Transverse - diagnosis ; Myelitis, Transverse - immunology ; Myelitis, Transverse - therapy ; Prognosis ; Recurrence ; Spinal Cord - immunology ; Spinal Cord - pathology</subject><ispartof>The Neurologist (Baltimore, Md.), 2005-01, Vol.11 (1), p.2-18</ispartof><rights>2005 Lippincott Williams & Wilkins, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15631640$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaplin, Adam I.</creatorcontrib><creatorcontrib>Krishnan, Chitra</creatorcontrib><creatorcontrib>Deshpande, Deepa M.</creatorcontrib><creatorcontrib>Pardo, Carlos A.</creatorcontrib><creatorcontrib>Kerr, Douglas A.</creatorcontrib><title>Diagnosis and Management of Acute Myelopathies</title><title>The Neurologist (Baltimore, Md.)</title><addtitle>Neurologist</addtitle><description>BACKGROUND:Acute myelopathies represent a heterogeneous group of disorders with distinct etiologies, clinical and radiologic features, and prognoses. Transverse myelitis (TM) is a prototype member of this group in which an immune-mediated process causes neural injury to the spinal cord, resulting in varying degrees of weakness, sensory alterations, and autonomic dysfunction. TM may exist as part of a multifocal CNS disease (eg, MS), multisystemic disease (eg, systemic lupus erythematosus), or as an isolated, idiopathic entity.
REVIEW SUMMARY:In this article, we summarize recent classification and diagnostic schemes, which provide a framework for the diagnosis and management of patients with acute myelopathy. Additionally, we review the state of current knowledge about the epidemiology, natural history, immunopathogenesis, and treatment strategies for patients with TM.
CONCLUSIONS:Our understanding of the classification, diagnosis, pathogenesis, and treatment of TM has recently begun to expand dramatically. With more rigorous criteria applied to distinguish acute myelopathies and with an emerging understanding of immunopathogenic events that underlie TM, it may now be possible to effectively initiate treatments in many of these disorders. Through the investigation of TM, we are also gaining a broader appreciation of the mechanisms that lead to autoimmune neurologic diseases in general.</description><subject>Acute Disease</subject><subject>Decision Trees</subject><subject>Diagnosis, Differential</subject><subject>Humans</subject><subject>Myelitis, Transverse - diagnosis</subject><subject>Myelitis, Transverse - immunology</subject><subject>Myelitis, Transverse - therapy</subject><subject>Prognosis</subject><subject>Recurrence</subject><subject>Spinal Cord - immunology</subject><subject>Spinal Cord - pathology</subject><issn>1074-7931</issn><issn>2331-2637</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kE1Lw0AQhhdRbK3-BQkevCXu7Gf2WOontHjRc9gkkza6-TCbUPrvXWmdywwvDwPvQ8gd0ASo0Q8UknZwCQ0DwhgtE25YCGl-RuaMc4iZ4vqczIFqEWvDYUauvP8KuFFMXJIZSMVBCTonyWNtt23nax_Ztow2trVbbLAdo66KlsU0YrQ5oOt6O-5q9NfkorLO481pL8jn89PH6jVev7-8rZbruIdUsDgtpNYiLWXOOP27WKmEBmswNSh5CqUudcE4KqCiKpktpBTSKJWnxkBV8AW5P_7th-5nQj9mTe0LdM622E0-U5oLIULXBbk9gVPeYJn1Q93Y4ZD9NwyAOAL7zo04-G837XHIdmjduMuCEqZTw2NGqaQQjMZ_Whn_BYFHYlc</recordid><startdate>200501</startdate><enddate>200501</enddate><creator>Kaplin, Adam I.</creator><creator>Krishnan, Chitra</creator><creator>Deshpande, Deepa M.</creator><creator>Pardo, Carlos A.</creator><creator>Kerr, Douglas A.</creator><general>Lippincott Williams & Wilkins, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200501</creationdate><title>Diagnosis and Management of Acute Myelopathies</title><author>Kaplin, Adam I. ; Krishnan, Chitra ; Deshpande, Deepa M. ; Pardo, Carlos A. ; Kerr, Douglas A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p1842-8c57748d5b23077482d6471a9e89e5381d7d7c23e6104fd2ac5545966b8991fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Acute Disease</topic><topic>Decision Trees</topic><topic>Diagnosis, Differential</topic><topic>Humans</topic><topic>Myelitis, Transverse - diagnosis</topic><topic>Myelitis, Transverse - immunology</topic><topic>Myelitis, Transverse - therapy</topic><topic>Prognosis</topic><topic>Recurrence</topic><topic>Spinal Cord - immunology</topic><topic>Spinal Cord - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaplin, Adam I.</creatorcontrib><creatorcontrib>Krishnan, Chitra</creatorcontrib><creatorcontrib>Deshpande, Deepa M.</creatorcontrib><creatorcontrib>Pardo, Carlos A.</creatorcontrib><creatorcontrib>Kerr, Douglas A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>The Neurologist (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaplin, Adam I.</au><au>Krishnan, Chitra</au><au>Deshpande, Deepa M.</au><au>Pardo, Carlos A.</au><au>Kerr, Douglas A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnosis and Management of Acute Myelopathies</atitle><jtitle>The Neurologist (Baltimore, Md.)</jtitle><addtitle>Neurologist</addtitle><date>2005-01</date><risdate>2005</risdate><volume>11</volume><issue>1</issue><spage>2</spage><epage>18</epage><pages>2-18</pages><issn>1074-7931</issn><eissn>2331-2637</eissn><abstract>BACKGROUND:Acute myelopathies represent a heterogeneous group of disorders with distinct etiologies, clinical and radiologic features, and prognoses. Transverse myelitis (TM) is a prototype member of this group in which an immune-mediated process causes neural injury to the spinal cord, resulting in varying degrees of weakness, sensory alterations, and autonomic dysfunction. TM may exist as part of a multifocal CNS disease (eg, MS), multisystemic disease (eg, systemic lupus erythematosus), or as an isolated, idiopathic entity.
REVIEW SUMMARY:In this article, we summarize recent classification and diagnostic schemes, which provide a framework for the diagnosis and management of patients with acute myelopathy. Additionally, we review the state of current knowledge about the epidemiology, natural history, immunopathogenesis, and treatment strategies for patients with TM.
CONCLUSIONS:Our understanding of the classification, diagnosis, pathogenesis, and treatment of TM has recently begun to expand dramatically. With more rigorous criteria applied to distinguish acute myelopathies and with an emerging understanding of immunopathogenic events that underlie TM, it may now be possible to effectively initiate treatments in many of these disorders. Through the investigation of TM, we are also gaining a broader appreciation of the mechanisms that lead to autoimmune neurologic diseases in general.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>15631640</pmid><doi>10.1097/01.nrl.0000149975.39201.0b</doi><tpages>17</tpages></addata></record> |
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source | MEDLINE; Journals@Ovid Complete |
subjects | Acute Disease Decision Trees Diagnosis, Differential Humans Myelitis, Transverse - diagnosis Myelitis, Transverse - immunology Myelitis, Transverse - therapy Prognosis Recurrence Spinal Cord - immunology Spinal Cord - pathology |
title | Diagnosis and Management of Acute Myelopathies |
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