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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-2013-27-10-4</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-27-10-4</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Paroxysmal 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>Electroclinical Subtypes of Cingulate Epilepsy</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>10</month>
<year>2013</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>15</day>
<month>10</month>
<year>2015</year>
</pub-date>
<volume>27</volume>
<issue>10</issue>
<fpage>75</fpage>
<lpage>76</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2013 The Author(s)</copyright-statement>
<copyright-year>2013</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="10.1001/jamaneurol.2013.2940" vol="70" page="995">
<article-title>Cingulate epilepsy: Report of 3 electroclinical subtypes with surgical outcomes</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Investigators from the Cleveland Clinic, and University of Texas Southwestern Medical Center, studied consecutive cases of cingulate gyrus epilepsy identified retrospectively from their epilepsy databases from 1992 to 2009.</p>
</abstract>
<kwd-group>
<kwd>Hypermotor/Hyperkinetic Seizures</kwd>
<kwd>Simple Motor Seizures</kwd>
<kwd>Posterior Cingulate Seizures</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Investigators from the Cleveland Clinic, and University of Texas Southwestern Medical Center, studied consecutive cases of cingulate gyrus epilepsy identified retrospectively from their epilepsy databases from 1992 to 2009. Of 14 patients with cingulate epilepsy confirmed by MRI and response to lesionectomy, 4 with lesions in the posterior cingulate location had electroclinical findings suggestive of a temporal origin of the epilepsy. Of 10 anterior cingulate cases, 6 in a typical (Bancaud) group had hypermotor/hyperkinetic seizures, rarely generalized, with fear, laughter, or severe interictal personality changes, and 4 were atypical, with simple motor seizures, frequently generalized, and a less favorable long-term surgical outcome. All atypical cases were associated with an underlying infiltrative astrocytoma. Posterior cingulate gyrus epilepsy is regarded as a pseudotemporal epilepsy. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENT. Surface EEG is often inaccurate in localizing a deep-seated epileptogenic zone in a patient with cingulate epilepsy. Symptoms of cingulate epilepsy are heterogeneous and dependent on an anterior or posterior localization of the lesion. Anterior lesions are associated with hyperkinetic behavior, cycling and running and gelastic seizures, expressed by mirthless laughter. Posterior cingulate seizures resemble temporal lobe epilepsy. This report emphasizes the importance of an MRI-identifiable lesion in the diagnosis of cingulate epilepsy.</p>
</body>
<back>
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</article>
