Anatomo‐electro‐clinical correlations: the Great Ormond Street Hospital, UK Case Report ‐ Case 05‐2008: Early‐onset symptomatic focal epilepsy: a dilemma in the timing of surgery
ABSTRACT [Case records of Epileptic Disorders. Anatomo‐electro‐clinical correlations. Case 05‐2008] We report the case of a six‐year‐old boy who presented in infancy with infantile spasms and left focal seizures. An MR scan at two months was suggestive of a right parietal cortical dysplasia, althoug...
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Veröffentlicht in: | Epileptic disorders 2008-12, Vol.10 (4), p.356-361 |
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creator | Desai, Neely Pressler, Ronit M. Jolleff, Nicola Clark, Maria Neville, Brian Eltze, Christin Harkness, William Cross, J. Helen |
description | ABSTRACT
[Case records of Epileptic Disorders. Anatomo‐electro‐clinical correlations. Case 05‐2008] We report the case of a six‐year‐old boy who presented in infancy with infantile spasms and left focal seizures. An MR scan at two months was suggestive of a right parietal cortical dysplasia, although this was less apparent on repeat scan at 11 months. The initial response to anti‐epileptic medications was good; surgery was therefore deferred at that time. Subsequently, seizure control fluctuated and developmental progress was, on the whole, good. However, ultimately seizures increased despite changing the AED, and he began showing developmental problems. Surgery was reconsidered. Again, a repeat MR scan did not define the lesion well. Following full further evaluation, including functional imaging that still implicated the right parietal cortex, subdural grid and depth electrode monitoring were undertaken at 6.5 years, which located the ictal onset zone deep within the lesion. This enabled a right inferior parietal lobe resection to be performed. Four years post‐surgery he remains seizure‐free and has shown progress in development. |
doi_str_mv | 10.1684/epd.2008.0214 |
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[Case records of Epileptic Disorders. Anatomo‐electro‐clinical correlations. Case 05‐2008] We report the case of a six‐year‐old boy who presented in infancy with infantile spasms and left focal seizures. An MR scan at two months was suggestive of a right parietal cortical dysplasia, although this was less apparent on repeat scan at 11 months. The initial response to anti‐epileptic medications was good; surgery was therefore deferred at that time. Subsequently, seizure control fluctuated and developmental progress was, on the whole, good. However, ultimately seizures increased despite changing the AED, and he began showing developmental problems. Surgery was reconsidered. Again, a repeat MR scan did not define the lesion well. Following full further evaluation, including functional imaging that still implicated the right parietal cortex, subdural grid and depth electrode monitoring were undertaken at 6.5 years, which located the ictal onset zone deep within the lesion. This enabled a right inferior parietal lobe resection to be performed. Four years post‐surgery he remains seizure‐free and has shown progress in development.</description><identifier>ISSN: 1294-9361</identifier><identifier>EISSN: 1950-6945</identifier><identifier>DOI: 10.1684/epd.2008.0214</identifier><language>eng</language><subject>child ; epilepsy surgery ; focal cortical dysplasia ; seizures ; telemetry</subject><ispartof>Epileptic disorders, 2008-12, Vol.10 (4), p.356-361</ispartof><rights>2008 International League Against Epilepsy</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1956-b35cdb7c524f4ee507941b896cfd873d8d7240244dd1a065f9a9528fea5632a63</citedby><cites>FETCH-LOGICAL-c1956-b35cdb7c524f4ee507941b896cfd873d8d7240244dd1a065f9a9528fea5632a63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1684%2Fepd.2008.0214$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1684%2Fepd.2008.0214$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Desai, Neely</creatorcontrib><creatorcontrib>Pressler, Ronit M.</creatorcontrib><creatorcontrib>Jolleff, Nicola</creatorcontrib><creatorcontrib>Clark, Maria</creatorcontrib><creatorcontrib>Neville, Brian</creatorcontrib><creatorcontrib>Eltze, Christin</creatorcontrib><creatorcontrib>Harkness, William</creatorcontrib><creatorcontrib>Cross, J. Helen</creatorcontrib><title>Anatomo‐electro‐clinical correlations: the Great Ormond Street Hospital, UK Case Report ‐ Case 05‐2008: Early‐onset symptomatic focal epilepsy: a dilemma in the timing of surgery</title><title>Epileptic disorders</title><description>ABSTRACT
[Case records of Epileptic Disorders. Anatomo‐electro‐clinical correlations. Case 05‐2008] We report the case of a six‐year‐old boy who presented in infancy with infantile spasms and left focal seizures. An MR scan at two months was suggestive of a right parietal cortical dysplasia, although this was less apparent on repeat scan at 11 months. The initial response to anti‐epileptic medications was good; surgery was therefore deferred at that time. Subsequently, seizure control fluctuated and developmental progress was, on the whole, good. However, ultimately seizures increased despite changing the AED, and he began showing developmental problems. Surgery was reconsidered. Again, a repeat MR scan did not define the lesion well. Following full further evaluation, including functional imaging that still implicated the right parietal cortex, subdural grid and depth electrode monitoring were undertaken at 6.5 years, which located the ictal onset zone deep within the lesion. This enabled a right inferior parietal lobe resection to be performed. Four years post‐surgery he remains seizure‐free and has shown progress in development.</description><subject>child</subject><subject>epilepsy surgery</subject><subject>focal cortical dysplasia</subject><subject>seizures</subject><subject>telemetry</subject><issn>1294-9361</issn><issn>1950-6945</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp9UEtu2zAUFIIGqJtk2f07QOWQFElJ3rmu80ENJMhnLdDkk8NCEgWSRaFdjtAD9TQ9Sai666zeDDhvhm-y7DMlSyorfomjWTJCqiVhlJ9kC1oLksuaiw8Js5rndSHpx-xTCD8IYemRLrI_60FF17u_r7-xQx39jHRnB6tVB9p5j52K1g1hBfEF4dqjinDnezcYeIweMcKNC6ONqvsCz99howLCA47OR0hWR05EgvPXVrBVvpsSS45pNUz9mOJTgobWzZE42g7HMK1AgUmw7xXY4V92tL0dDuBaCD_9Af10np22qgt48X-eZc9X26fNTb67u77drHe5ThXIfF8IbfalFoy3HFGQsuZ0X9VSt6YqC1OZknHCODeGKiJFW6tasKpFJWTBlCzOsvzoq70LwWPbjN72yk8NJc1cfZOqb-b7mrn6pJdH_a90wPS-uNnef2NfrxItZfEG1d2OqQ</recordid><startdate>200812</startdate><enddate>200812</enddate><creator>Desai, Neely</creator><creator>Pressler, Ronit M.</creator><creator>Jolleff, Nicola</creator><creator>Clark, Maria</creator><creator>Neville, Brian</creator><creator>Eltze, Christin</creator><creator>Harkness, William</creator><creator>Cross, J. Helen</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200812</creationdate><title>Anatomo‐electro‐clinical correlations: the Great Ormond Street Hospital, UK Case Report ‐ Case 05‐2008: Early‐onset symptomatic focal epilepsy: a dilemma in the timing of surgery</title><author>Desai, Neely ; Pressler, Ronit M. ; Jolleff, Nicola ; Clark, Maria ; Neville, Brian ; Eltze, Christin ; Harkness, William ; Cross, J. Helen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1956-b35cdb7c524f4ee507941b896cfd873d8d7240244dd1a065f9a9528fea5632a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>child</topic><topic>epilepsy surgery</topic><topic>focal cortical dysplasia</topic><topic>seizures</topic><topic>telemetry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Desai, Neely</creatorcontrib><creatorcontrib>Pressler, Ronit M.</creatorcontrib><creatorcontrib>Jolleff, Nicola</creatorcontrib><creatorcontrib>Clark, Maria</creatorcontrib><creatorcontrib>Neville, Brian</creatorcontrib><creatorcontrib>Eltze, Christin</creatorcontrib><creatorcontrib>Harkness, William</creatorcontrib><creatorcontrib>Cross, J. Helen</creatorcontrib><collection>CrossRef</collection><jtitle>Epileptic disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Desai, Neely</au><au>Pressler, Ronit M.</au><au>Jolleff, Nicola</au><au>Clark, Maria</au><au>Neville, Brian</au><au>Eltze, Christin</au><au>Harkness, William</au><au>Cross, J. Helen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anatomo‐electro‐clinical correlations: the Great Ormond Street Hospital, UK Case Report ‐ Case 05‐2008: Early‐onset symptomatic focal epilepsy: a dilemma in the timing of surgery</atitle><jtitle>Epileptic disorders</jtitle><date>2008-12</date><risdate>2008</risdate><volume>10</volume><issue>4</issue><spage>356</spage><epage>361</epage><pages>356-361</pages><issn>1294-9361</issn><eissn>1950-6945</eissn><abstract>ABSTRACT
[Case records of Epileptic Disorders. Anatomo‐electro‐clinical correlations. Case 05‐2008] We report the case of a six‐year‐old boy who presented in infancy with infantile spasms and left focal seizures. An MR scan at two months was suggestive of a right parietal cortical dysplasia, although this was less apparent on repeat scan at 11 months. The initial response to anti‐epileptic medications was good; surgery was therefore deferred at that time. Subsequently, seizure control fluctuated and developmental progress was, on the whole, good. However, ultimately seizures increased despite changing the AED, and he began showing developmental problems. Surgery was reconsidered. Again, a repeat MR scan did not define the lesion well. Following full further evaluation, including functional imaging that still implicated the right parietal cortex, subdural grid and depth electrode monitoring were undertaken at 6.5 years, which located the ictal onset zone deep within the lesion. This enabled a right inferior parietal lobe resection to be performed. Four years post‐surgery he remains seizure‐free and has shown progress in development.</abstract><doi>10.1684/epd.2008.0214</doi><tpages>6</tpages></addata></record> |
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source | Access via Wiley Online Library; John Libbey Eurotext Journals; EZB-FREE-00999 freely available EZB journals |
subjects | child epilepsy surgery focal cortical dysplasia seizures telemetry |
title | Anatomo‐electro‐clinical correlations: the Great Ormond Street Hospital, UK Case Report ‐ Case 05‐2008: Early‐onset symptomatic focal epilepsy: a dilemma in the timing of surgery |
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