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<front>
<journal-meta>
<journal-id journal-id-type="issn">1043-3155</journal-id>
<journal-id journal-id-type="nlm-ta">Pediatr Neurol Briefs</journal-id>
<journal-id journal-id-type="pmc">pedneurbriefs</journal-id>
<journal-id journal-id-type="iso-abbrev">Pediatr Neurol Briefs</journal-id>
<journal-title-group>
<journal-title>Pediatric Neurology Briefs</journal-title>
<abbrev-journal-title>Pediatr Neurol Briefs</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2166-6482</issn>
<issn pub-type="ppub">1043-3155</issn>
<issn-l>2166-3155</issn-l>
<publisher>
<publisher-name>Pediatric Neurology Briefs Publishers</publisher-name>
<publisher-loc>Chicago, IL, USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">PNB-23-89</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-23-12-1</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Developmental Disorders</subject>
</subj-group>
<subj-group subj-group-type="Discipline-v2">
<subject>Neurology</subject>
<subject>Pediatrics</subject>
<subject>Nervous System Diseases</subject>
<subject>Child Development</subject>
<subject>Brain Diseases</subject>
<subject>Neurosurgery</subject>
<subject>Child</subject>
<subject>Infant</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Epileptogenicity of Cortical Dysplasias and Tumors</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0002-0173-7931</contrib-id>
<name>
<surname>Millichap</surname>
<given-names>J. Gordon</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
<xref ref-type="aff" rid="AF0002">2</xref>
<xref ref-type="corresp" rid="cor1">&#x002A;</xref>
</contrib>
</contrib-group>
<aff id="AF0001">
<label>1</label>Division of Neurology, Ann &#x0026; Robert H. Lurie Children&#x0027;s Hospital of Chicago, Chicago, IL</aff>
<aff id="AF0002">
<label>2</label>Departments of Pediatrics and Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL</aff>
<author-notes>
<corresp id="cor1"><label>&#x002A;</label>Correspondence: Dr. J. Gordon Millichap, E-mail: <email xlink:href="jgmillichap@northwestern.edu">jgmillichap@northwestern.edu</email>
</corresp>
</author-notes>
<pub-date date-type="pub" publication-format="print">
<month>12</month>
<year>2009</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>12</month>
<year>2015</year>
</pub-date>
<volume>23</volume>
<issue>12</issue>
<fpage>89</fpage>
<lpage>90</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2009 The Author(s)</copyright-statement>
<copyright-year>2009</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
<license-p>This work is licensed under the <uri xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</uri>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<related-article id="R1" related-article-type="commentary-article" ext-link-type="doi" xlink:href="10.1093/brain/awp242" vol="132" page="3072">
<article-title>Local and remote epileptogenicity in focal cortical dysplasias and neurodevelopmental tumours</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>The epileptogenic characteristic of focal cortical dysplasias and dysembryoplastic neuroepithelial tumors explored by depth electrodes and stereoelectroencephalography is quantified using an epileptogenicity index, in a study of 36 patients with focal drug-resistant epilepsy at Universite de la Mediterranee and other centers in Marseille and Rennes, France.</p>
</abstract>
<kwd-group>
<kwd>Epileptogenicity Index</kwd>
<kwd>Maximal Epileptogenicity</kwd>
<kwd>Cortical Dysplasias</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>The epileptogenic characteristic of focal cortical dysplasias and dysembryoplastic neuroepithelial tumors explored by depth electrodes and stereoelectroencephalography is quantified using an epileptogenicity index, in a study of 36 patients with focal drug-resistant epilepsy at Universite de la Mediterranee and other centers in Marseille and Rennes, France. The epileptogenic zone is organized as a simple focal lesional site or as a complex &#x2018;epileptogenic network&#x2019; extending beyond the lesion. Epileptogenicity index (EI) values range from 0 (none) to 1 (maximal epileptogenicity). The mean EI in lesional regions was 0.87, and 0.29 in non-lesional structures. A single focal lesion was found in 31% of patients, and more than one epileptogenic region in 25 patients (64%) (a network organization in 61% and bilateral epileptogenic zone organization in 8%). Distant structures are often involved, and in mesio-temporal epilepsy, the number of epileptogenic structures increases with epilepsy duration. None patient with bilateral organization became seizure-free, while 87% with focal organization and 57% with network organization were seizure-free. The EI is of value in the delineation of the epileptogenic zone with brain lesions and in the definition of the extent of surgical resection. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. The epileptogenicity index (EI) is a method of quantifying and defining the epileptogenicity in and around focal cortical dysplasias and neurodevelopmntal tumors during stereo-EEG with depth electrodes. Defining the extent of the epileptogenic zone is important in prognosis and in surgical resection. The November 2009 issue of <bold>Ped Neur Briefs</bold> reviews a report of a novel immunocytochemical test for epileptogenic brain tissue, independent of the histological findings [<xref ref-type="bibr" rid="CIT0002">2</xref>]. With this added quantification of the epileptogenicity zone by stereo-EEG and the EI, surgical resection for refractory epilepsies should become more accurate and effective.</p>
</body>
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