<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.0 20120330//EN" "http://jats.nlm.nih.gov/publishing/1.0/JATS-journalpublishing1.dtd">
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="article-commentary" dtd-version="1.0" xml:lang="en">
<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-2014-28-8-8</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-28-8-8</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Encephalitis / Encephalopathy</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>Dysplastic Neurons in Ovarian Teratomas in NMDAR Encephalitis</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 contrib-type="author">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0002-0798-0131</contrib-id>
<name>
<surname>Millichap</surname>
<given-names>John J.</given-names>
</name>
<degrees>MD</degrees>
<xref ref-type="aff" rid="AF0001">1</xref>
<xref ref-type="aff" rid="AF0002">2</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>08</month>
<year>2014</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>31</day>
<month>10</month>
<year>2015</year>
</pub-date>
<volume>28</volume>
<issue>8</issue>
<fpage>62</fpage>
<lpage>63</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 2014 The Author(s)</copyright-statement>
<copyright-year>2014</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.2014.488" vol="71" page="717">
<article-title>Abnormal neurons in teratomas in NMDAR encephalitis</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Investigators at University of Toronto, Canada, report detection of atypical (dysplastic) neuronal elements in 4 of 5 teratomas resected from cases with NMDAR encephalitis but not in 39 controls.</p>
</abstract>
<kwd-group>
<kwd>Dysplastic</kwd>
<kwd>Gangliogliomas</kwd>
<kwd>Encephalitic</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Investigators at University of Toronto, Canada, report detection of atypical (dysplastic) neuronal elements in 4 of 5 teratomas resected from cases with NMDAR encephalitis but not in 39 controls. These atypical neurons resembled gangliogliomas (n = 3) or ganglioneuroblastoma (n = 1). Abnormal neuroglial elements were closely related to immune infiltrates resected from 4 of 4 cases. Abnormal neurons within teratomas distinguish cases with NMDAR encephalitis from controls and may promote the development of autoimmunity. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENTARY. The authors propose that pathological examination of teratomas removed from patients with NMDAR encephalitis should first focus on areas containing CNS tissue and second on neurons closely approximated by inflammatory infiltrates. The colocalization of dysplastic CNS neurons and inflammatory infiltrates support an autoimmune cause for the clinical encephalitic presentation [<xref ref-type="bibr" rid="CIT0001">1</xref>].</p>
<sec id="S0001">
<title>Broca&#x0027;s aphasia: a new phenotype of anti NMDAR encephalitis</title>
<p>Investigators at Le Kremlin-Bicetre and centers in Paris, France, report a novel case of anti NMDAR encephalitis in a 4-year-old girl who presented with partial seizures that evolved to sudden and isolated Broca&#x0027;s aphasia and subsequently resolved. Anti NMDAR antibodies were positive in CSF and serum [<xref ref-type="bibr" rid="CIT0002">2</xref>].</p>
</sec>
</body>
<back>
<ref-list>
<ref id="CIT0001">
<label>1</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Day</surname>
<given-names>GS</given-names>
</name>
<name>
<surname>Laiq</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Tang-Wai</surname>
<given-names>DF</given-names>
</name>
<name>
<surname>Munoz</surname>
<given-names>DG</given-names>
</name>
</person-group>
<article-title>Abnormal neurons in teratomas in NMDAR encephalitis</article-title>
<source>JAMA Neurol</source>
<year>2014</year>
<month>Jun</month>
<volume>71</volume>
<issue>6</issue>
<fpage>717</fpage>
<lpage>24</lpage>
<pub-id pub-id-type="doi">10.1001/jamaneurol.2014.488</pub-id>
<pub-id pub-id-type="pmid">24781184</pub-id>
</element-citation>
</ref>
<ref id="CIT0002">
<label>2</label>
<element-citation publication-type="confproc">
<person-group person-group-type="author">
<name>
<surname>Deiva</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Pera</surname>
<given-names>MC</given-names>
</name>
<name>
<surname>Maurey</surname>
<given-names>H</given-names>
</name>
<name>
<surname>Chr&#x00E9;tien</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Archambaud</surname>
<given-names>F</given-names>
</name>
<name>
<surname>Bouilleret</surname>
<given-names>V</given-names>
</name>
</person-group>
<article-title>Sudden and isolated Broca&#x0027;s aphasia: a new clinical phenotype of anti NMDA receptor antibodies encephalitis in children</article-title>
<source>Eur J Paediatr Neurol</source>
<year>2014</year>
<month>Jun</month>
<day>11</day>
<comment>Epub ahead of print</comment>
<pub-id pub-id-type="doi">10.1016/j.ejpn.2014.06.002</pub-id>
<pub-id pub-id-type="pmid">24980905</pub-id>
</element-citation>
</ref>
</ref-list>
</back>
</article>