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Corpus callosotomy: A palliative therapeutic technique may help identify resectable epileptogenic foci
Summary Corpus callosotomy has a long history as a palliative treatment for intractable epilepsy. Identification of a single epileptogenic zone is critical to performing successful resective surgery. We describe three patients in which corpus callosotomy allowed recognition of unapparent seizure foc...
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Published in: | Seizure (London, England) England), 2007-09, Vol.16 (6), p.545-553 |
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description | Summary Corpus callosotomy has a long history as a palliative treatment for intractable epilepsy. Identification of a single epileptogenic zone is critical to performing successful resective surgery. We describe three patients in which corpus callosotomy allowed recognition of unapparent seizure foci, leading to subsequent successful resection. We retrospectively reviewed our epilepsy surgery database from 2003 to 2005 for children who had a prior callosotomy and were candidates for focal resection. All underwent magnetic resonance imaging and scalp video electroencephalograph monitoring, and two had magnetoencephalography, electrocorticography and/or intracranial video electroencephalograph monitoring. The children were 8 and 9 years old, and seizure onset varied from early infancy to early childhood. One child had a history of head trauma preceding seizure onset, one had a large intracerebral infarct and dysplastic cortex in the contralateral frontal lobe, and the other had an anterior temporal lobe resection without improvement in seizure frequency. After medical management failed, callosotomy was performed with the expectation of decreasing the seizure types affecting both hemispheres. Following transection of the callosal fibers, a single focus was recognized and resected, with resultant dramatic improvement in seizure control. In medically refractory epilepsy, where rapid secondary bisynchrony is suspected but the electroencephalograph is non-localizing, callosotomy should be considered as a means of treating generalized seizure types, but may also assist in identifying potentially operable seizure foci. Study limitations include its retrospective nature and cohort size. The findings, however, suggest the need for prospective, systematic, well-controlled studies of the use of corpus callostomy in this intractable patient population. |
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Identification of a single epileptogenic zone is critical to performing successful resective surgery. We describe three patients in which corpus callosotomy allowed recognition of unapparent seizure foci, leading to subsequent successful resection. We retrospectively reviewed our epilepsy surgery database from 2003 to 2005 for children who had a prior callosotomy and were candidates for focal resection. All underwent magnetic resonance imaging and scalp video electroencephalograph monitoring, and two had magnetoencephalography, electrocorticography and/or intracranial video electroencephalograph monitoring. The children were 8 and 9 years old, and seizure onset varied from early infancy to early childhood. One child had a history of head trauma preceding seizure onset, one had a large intracerebral infarct and dysplastic cortex in the contralateral frontal lobe, and the other had an anterior temporal lobe resection without improvement in seizure frequency. After medical management failed, callosotomy was performed with the expectation of decreasing the seizure types affecting both hemispheres. Following transection of the callosal fibers, a single focus was recognized and resected, with resultant dramatic improvement in seizure control. In medically refractory epilepsy, where rapid secondary bisynchrony is suspected but the electroencephalograph is non-localizing, callosotomy should be considered as a means of treating generalized seizure types, but may also assist in identifying potentially operable seizure foci. Study limitations include its retrospective nature and cohort size. The findings, however, suggest the need for prospective, systematic, well-controlled studies of the use of corpus callostomy in this intractable patient population.</description><identifier>ISSN: 1059-1311</identifier><identifier>EISSN: 1532-2688</identifier><identifier>DOI: 10.1016/j.seizure.2007.04.004</identifier><identifier>PMID: 17521926</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Child ; Corpus callosotomy ; Corpus Callosum - surgery ; Electroencephalography ; Epilepsy - diagnosis ; Epilepsy - therapy ; Epilepsy surgery ; Female ; Humans ; Intractable epilepsy ; Magnetic Resonance Imaging ; Magnetoencephalography - methods ; Male ; Neurology ; Palliative Care - methods ; Pediatric epilepsy ; Retrospective Studies ; Seizure</subject><ispartof>Seizure (London, England), 2007-09, Vol.16 (6), p.545-553</ispartof><rights>British Epilepsy Association</rights><rights>2007 British Epilepsy Association</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c531t-6d4d9bb98e6247c17f190b86c2adbb965ba0746f86b92f534d87024a29f62b613</citedby><cites>FETCH-LOGICAL-c531t-6d4d9bb98e6247c17f190b86c2adbb965ba0746f86b92f534d87024a29f62b613</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/17521926$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Clarke, Dave F</creatorcontrib><creatorcontrib>Wheless, James W</creatorcontrib><creatorcontrib>Chacon, Monica M</creatorcontrib><creatorcontrib>Breier, Joshua</creatorcontrib><creatorcontrib>Koenig, Mary-Kay</creatorcontrib><creatorcontrib>McManis, Mark</creatorcontrib><creatorcontrib>Castillo, Edward</creatorcontrib><creatorcontrib>Baumgartner, James E</creatorcontrib><title>Corpus callosotomy: A palliative therapeutic technique may help identify resectable epileptogenic foci</title><title>Seizure (London, England)</title><addtitle>Seizure</addtitle><description>Summary Corpus callosotomy has a long history as a palliative treatment for intractable epilepsy. Identification of a single epileptogenic zone is critical to performing successful resective surgery. We describe three patients in which corpus callosotomy allowed recognition of unapparent seizure foci, leading to subsequent successful resection. We retrospectively reviewed our epilepsy surgery database from 2003 to 2005 for children who had a prior callosotomy and were candidates for focal resection. All underwent magnetic resonance imaging and scalp video electroencephalograph monitoring, and two had magnetoencephalography, electrocorticography and/or intracranial video electroencephalograph monitoring. The children were 8 and 9 years old, and seizure onset varied from early infancy to early childhood. One child had a history of head trauma preceding seizure onset, one had a large intracerebral infarct and dysplastic cortex in the contralateral frontal lobe, and the other had an anterior temporal lobe resection without improvement in seizure frequency. After medical management failed, callosotomy was performed with the expectation of decreasing the seizure types affecting both hemispheres. Following transection of the callosal fibers, a single focus was recognized and resected, with resultant dramatic improvement in seizure control. In medically refractory epilepsy, where rapid secondary bisynchrony is suspected but the electroencephalograph is non-localizing, callosotomy should be considered as a means of treating generalized seizure types, but may also assist in identifying potentially operable seizure foci. Study limitations include its retrospective nature and cohort size. The findings, however, suggest the need for prospective, systematic, well-controlled studies of the use of corpus callostomy in this intractable patient population.</description><subject>Child</subject><subject>Corpus callosotomy</subject><subject>Corpus Callosum - surgery</subject><subject>Electroencephalography</subject><subject>Epilepsy - diagnosis</subject><subject>Epilepsy - therapy</subject><subject>Epilepsy surgery</subject><subject>Female</subject><subject>Humans</subject><subject>Intractable epilepsy</subject><subject>Magnetic Resonance Imaging</subject><subject>Magnetoencephalography - methods</subject><subject>Male</subject><subject>Neurology</subject><subject>Palliative Care - methods</subject><subject>Pediatric epilepsy</subject><subject>Retrospective Studies</subject><subject>Seizure</subject><issn>1059-1311</issn><issn>1532-2688</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkU-P1SAUxYnROOPoR9CwctcKFGjrQjN5Gf8kk7hQ14TSi48nLRXoJPXTS_NeYuLGFRdyzr3c30HoJSU1JVS-OdUJ3O81Qs0IaWvCa0L4I3RNRcMqJrvucamJ6CvaUHqFnqV0IoT0nDZP0RVtBaM9k9fIHkJc1oSN9j6kkMO0vcW3eClXp7N7AJyPEPUCa3YGZzDH2f1aAU96w0fwC3YjzNnZDUdIYLIePGBYnIclhx8wF5MNxj1HT6z2CV5czhv0_cPdt8On6v7Lx8-H2_vKiIbmSo587Ieh70Ay3hraWtqToZOG6bE8SzFo0nJpOzn0zIqGj11LGNest5INkjY36PW57xJD-WbKanLJgPd6hrAmJTsqJBW7UJyFJoaUIli1RDfpuClK1A5YndQFsNoBK8JVAVx8ry4D1mGC8a_rQrQI3p8FUNZ8cBBVMg5mA6OLhY8ag_vviHf_dDDeFZDa_4QN0imscS4MFVWJKaK-7invIZO2BNxJ2fwBCmWlyw</recordid><startdate>20070901</startdate><enddate>20070901</enddate><creator>Clarke, Dave F</creator><creator>Wheless, James W</creator><creator>Chacon, Monica M</creator><creator>Breier, Joshua</creator><creator>Koenig, Mary-Kay</creator><creator>McManis, Mark</creator><creator>Castillo, Edward</creator><creator>Baumgartner, James E</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</scope><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>20070901</creationdate><title>Corpus callosotomy: A palliative therapeutic technique may help identify resectable epileptogenic foci</title><author>Clarke, Dave F ; Wheless, James W ; Chacon, Monica M ; Breier, Joshua ; Koenig, Mary-Kay ; McManis, Mark ; Castillo, Edward ; Baumgartner, James E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c531t-6d4d9bb98e6247c17f190b86c2adbb965ba0746f86b92f534d87024a29f62b613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Child</topic><topic>Corpus callosotomy</topic><topic>Corpus Callosum - surgery</topic><topic>Electroencephalography</topic><topic>Epilepsy - diagnosis</topic><topic>Epilepsy - therapy</topic><topic>Epilepsy surgery</topic><topic>Female</topic><topic>Humans</topic><topic>Intractable epilepsy</topic><topic>Magnetic Resonance Imaging</topic><topic>Magnetoencephalography - methods</topic><topic>Male</topic><topic>Neurology</topic><topic>Palliative Care - methods</topic><topic>Pediatric epilepsy</topic><topic>Retrospective Studies</topic><topic>Seizure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Clarke, Dave F</creatorcontrib><creatorcontrib>Wheless, James W</creatorcontrib><creatorcontrib>Chacon, Monica M</creatorcontrib><creatorcontrib>Breier, Joshua</creatorcontrib><creatorcontrib>Koenig, Mary-Kay</creatorcontrib><creatorcontrib>McManis, Mark</creatorcontrib><creatorcontrib>Castillo, Edward</creatorcontrib><creatorcontrib>Baumgartner, James E</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>Seizure (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Clarke, Dave F</au><au>Wheless, James W</au><au>Chacon, Monica M</au><au>Breier, Joshua</au><au>Koenig, Mary-Kay</au><au>McManis, Mark</au><au>Castillo, Edward</au><au>Baumgartner, James E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Corpus callosotomy: A palliative therapeutic technique may help identify resectable epileptogenic foci</atitle><jtitle>Seizure (London, England)</jtitle><addtitle>Seizure</addtitle><date>2007-09-01</date><risdate>2007</risdate><volume>16</volume><issue>6</issue><spage>545</spage><epage>553</epage><pages>545-553</pages><issn>1059-1311</issn><eissn>1532-2688</eissn><abstract>Summary Corpus callosotomy has a long history as a palliative treatment for intractable epilepsy. Identification of a single epileptogenic zone is critical to performing successful resective surgery. We describe three patients in which corpus callosotomy allowed recognition of unapparent seizure foci, leading to subsequent successful resection. We retrospectively reviewed our epilepsy surgery database from 2003 to 2005 for children who had a prior callosotomy and were candidates for focal resection. All underwent magnetic resonance imaging and scalp video electroencephalograph monitoring, and two had magnetoencephalography, electrocorticography and/or intracranial video electroencephalograph monitoring. The children were 8 and 9 years old, and seizure onset varied from early infancy to early childhood. One child had a history of head trauma preceding seizure onset, one had a large intracerebral infarct and dysplastic cortex in the contralateral frontal lobe, and the other had an anterior temporal lobe resection without improvement in seizure frequency. After medical management failed, callosotomy was performed with the expectation of decreasing the seizure types affecting both hemispheres. Following transection of the callosal fibers, a single focus was recognized and resected, with resultant dramatic improvement in seizure control. In medically refractory epilepsy, where rapid secondary bisynchrony is suspected but the electroencephalograph is non-localizing, callosotomy should be considered as a means of treating generalized seizure types, but may also assist in identifying potentially operable seizure foci. Study limitations include its retrospective nature and cohort size. The findings, however, suggest the need for prospective, systematic, well-controlled studies of the use of corpus callostomy in this intractable patient population.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>17521926</pmid><doi>10.1016/j.seizure.2007.04.004</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Child Corpus callosotomy Corpus Callosum - surgery Electroencephalography Epilepsy - diagnosis Epilepsy - therapy Epilepsy surgery Female Humans Intractable epilepsy Magnetic Resonance Imaging Magnetoencephalography - methods Male Neurology Palliative Care - methods Pediatric epilepsy Retrospective Studies Seizure |
title | Corpus callosotomy: A palliative therapeutic technique may help identify resectable epileptogenic foci |
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