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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-16-71-b</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-16-9-9</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>Simplified Classification of Focal Cortical Dysplasia</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, Children&#x0027;s Memorial Hospital, 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>09</month>
<year>2002</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>04</month>
<year>2016</year>
</pub-date>
<volume>16</volume>
<issue>9</issue>
<fpage>71</fpage>
<lpage>72</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2002 The Author(s)</copyright-statement>
<copyright-year>2002</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/awf175" vol="125" page="1719">
<article-title>Focal cortical dysplasia: neuropathological subtypes, EEG, neuroimaging and surgical outcome</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Sections of cortex from 52 of 224 (23%) patients with cortical dysplasia, operated on for drug-resistant partial epilepsy, were retrospectively re-examined histologically at Niguarda Hospital, and Istituto Nazionale Neurologico &#x2018;C. Besta&#x2019;, Milan, Italy.</p>
</abstract>
<kwd-group>
<kwd>Focal Cortical Dysplasia</kwd>
<kwd>Architectural Dysplasia</kwd>
<kwd>Taylor-Type Cortical Dysplasia</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Sections of cortex from 52 of 224 (23%) patients with cortical dysplasia, operated on for drug-resistant partial epilepsy, were retrospectively re-examined histologically at Niguarda Hospital, and Istituto Nazionale Neurologico &#x2018;C. Besta&#x2019;, Milan, Italy. Three subgroups were identified as follows: 1) architectural dysplasia (31 patients) with abnormal cortical lamination and ectopic neurons in white matter; 2) cytoarchitectural dysplasia (6 patients) with altered cortical lamination and giant neurofilament-enriched neurons; and 3) Taylor-type cortical dysplasia (15 patients) with cortical laminar disruption and giant dysmorphic neurons and balloon cells. Group 1 architectural dysplasia cases had a temporal lobe location for the epileptogenic zone, with focal hypoplasia, and a significantly lower seizure frequency than groups 2 and 3. Group 3 Taylor-type dysplasia patients had an extratemporal epileptogenic zone, interictal distinctive stereo-EEG with high frequency fast spikes and polyspikes interspersed with fast low amplitude activity, and MRI signal alterations with thickening of cortex, blurred grey-white matter junction and hyperintensity of subcortical white matter. Group 3 Taylor-type had the best outcome, with 75% seizure-free after one year follow-up, compared with 50% in type 2 cytoarchitectural cases, and 43% seizure-free in type 1 architectural dysplasia cases. The three-category classification has easily recognized histopathological findings, and clinically homogeneous characteristics. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. In the above series of focal cortical dysplasia, the video or stereo-EEG provided the best delineation of the epileptogenic zone, superior to the MRI. In one-third of cases, the MRI was unremarkable, and in those with MRI evidence of a lesion, the boundaries were ill-defined. Type 3 Taylor-type dysplasia had a better outcome than the type 1 architectural and type 2 cytoarchitectural dysplasias.</p>
</body>
<back>
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