Neuroimaging yield in isolated Horner syndrome
PURPOSE OF REVIEWTo review the yield of imaging in isolated cases of Horner syndrome in order to better understand if and when imaging will ultimately be beneficial. RECENT FINDINGSImaging in Horner syndrome is commonly performed, however, imaging yield in isolated Horner syndrome has not been exten...
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Veröffentlicht in: | Current opinion in ophthalmology 2011-11, Vol.22 (6), p.468-471 |
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creator | Al-Moosa, Ashref Eggenberger, Eric |
description | PURPOSE OF REVIEWTo review the yield of imaging in isolated cases of Horner syndrome in order to better understand if and when imaging will ultimately be beneficial.
RECENT FINDINGSImaging in Horner syndrome is commonly performed, however, imaging yield in isolated Horner syndrome has not been extensively studied. A few studies have tried to look into the yield of imaging in such cases and derive conclusions from their findings.
SUMMARYWith limited evidence-based data, the general recommendation for evaluation in pediatric cases of isolated Horner syndrome is physical examination, urinary catecholamines and imaging. In adults, it may be possible to hold-off on imaging of isolated Horner syndrome especially if evidence exists establishing chronic duration. |
doi_str_mv | 10.1097/ICU.0b013e32834bbf06 |
format | Article |
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RECENT FINDINGSImaging in Horner syndrome is commonly performed, however, imaging yield in isolated Horner syndrome has not been extensively studied. A few studies have tried to look into the yield of imaging in such cases and derive conclusions from their findings.
SUMMARYWith limited evidence-based data, the general recommendation for evaluation in pediatric cases of isolated Horner syndrome is physical examination, urinary catecholamines and imaging. In adults, it may be possible to hold-off on imaging of isolated Horner syndrome especially if evidence exists establishing chronic duration.</description><identifier>ISSN: 1040-8738</identifier><identifier>EISSN: 1531-7021</identifier><identifier>DOI: 10.1097/ICU.0b013e32834bbf06</identifier><identifier>PMID: 21918445</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins, Inc</publisher><subject>Horner Syndrome - diagnosis ; Humans ; Neuroimaging</subject><ispartof>Current opinion in ophthalmology, 2011-11, Vol.22 (6), p.468-471</ispartof><rights>2011 Lippincott Williams & Wilkins, Inc.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3556-3e5a403aef0f4c54ee22eef863a05a45abdc09c8ef3ddb9a12c265b0fe8432d33</citedby><cites>FETCH-LOGICAL-c3556-3e5a403aef0f4c54ee22eef863a05a45abdc09c8ef3ddb9a12c265b0fe8432d33</cites></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/21918445$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Al-Moosa, Ashref</creatorcontrib><creatorcontrib>Eggenberger, Eric</creatorcontrib><title>Neuroimaging yield in isolated Horner syndrome</title><title>Current opinion in ophthalmology</title><addtitle>Curr Opin Ophthalmol</addtitle><description>PURPOSE OF REVIEWTo review the yield of imaging in isolated cases of Horner syndrome in order to better understand if and when imaging will ultimately be beneficial.
RECENT FINDINGSImaging in Horner syndrome is commonly performed, however, imaging yield in isolated Horner syndrome has not been extensively studied. A few studies have tried to look into the yield of imaging in such cases and derive conclusions from their findings.
SUMMARYWith limited evidence-based data, the general recommendation for evaluation in pediatric cases of isolated Horner syndrome is physical examination, urinary catecholamines and imaging. In adults, it may be possible to hold-off on imaging of isolated Horner syndrome especially if evidence exists establishing chronic duration.</description><subject>Horner Syndrome - diagnosis</subject><subject>Humans</subject><subject>Neuroimaging</subject><issn>1040-8738</issn><issn>1531-7021</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1PwzAMhiMEYmPwDxDqjVNHPrv0iCZgkya4sHOUNs5WSJuRtJr27wkacOCAZMm2_Pi1_CJ0TfCU4HJ2t5yvp7jChAGjkvGqsrg4QWMiGMlnmJLTVGOOczljcoQuYnzDOPVSnKMRJSWRnIsxmj7DEHzT6k3TbbJDA85kTZc10Tvdg8kWPnQQsnjoTPAtXKIzq12Eq-88QevHh9f5Il-9PC3n96u8ZkIUOQOhOWYaLLa8FhyAUgArC6ZxmghdmRqXtQTLjKlKTWhNC1FhC5IzahiboNuj7i74jwFir9om1uCc7sAPUcmyJDQFTSQ_knXwMQawahfSO-GgCFZfRqlklPprVFq7-T4wVC2Y36UfZxIgj8Deux5CfHfDHoLagnb99n_tTwHyd2g</recordid><startdate>201111</startdate><enddate>201111</enddate><creator>Al-Moosa, Ashref</creator><creator>Eggenberger, Eric</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>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201111</creationdate><title>Neuroimaging yield in isolated Horner syndrome</title><author>Al-Moosa, Ashref ; Eggenberger, Eric</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3556-3e5a403aef0f4c54ee22eef863a05a45abdc09c8ef3ddb9a12c265b0fe8432d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Horner Syndrome - diagnosis</topic><topic>Humans</topic><topic>Neuroimaging</topic><toplevel>online_resources</toplevel><creatorcontrib>Al-Moosa, Ashref</creatorcontrib><creatorcontrib>Eggenberger, Eric</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Current opinion in ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Al-Moosa, Ashref</au><au>Eggenberger, Eric</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuroimaging yield in isolated Horner syndrome</atitle><jtitle>Current opinion in ophthalmology</jtitle><addtitle>Curr Opin Ophthalmol</addtitle><date>2011-11</date><risdate>2011</risdate><volume>22</volume><issue>6</issue><spage>468</spage><epage>471</epage><pages>468-471</pages><issn>1040-8738</issn><eissn>1531-7021</eissn><abstract>PURPOSE OF REVIEWTo review the yield of imaging in isolated cases of Horner syndrome in order to better understand if and when imaging will ultimately be beneficial.
RECENT FINDINGSImaging in Horner syndrome is commonly performed, however, imaging yield in isolated Horner syndrome has not been extensively studied. A few studies have tried to look into the yield of imaging in such cases and derive conclusions from their findings.
SUMMARYWith limited evidence-based data, the general recommendation for evaluation in pediatric cases of isolated Horner syndrome is physical examination, urinary catecholamines and imaging. In adults, it may be possible to hold-off on imaging of isolated Horner syndrome especially if evidence exists establishing chronic duration.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>21918445</pmid><doi>10.1097/ICU.0b013e32834bbf06</doi><tpages>4</tpages></addata></record> |
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source | MEDLINE; Journals@Ovid Complete |
subjects | Horner Syndrome - diagnosis Humans Neuroimaging |
title | Neuroimaging yield in isolated Horner syndrome |
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