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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-3-76</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-3-10-5</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Intracranial Tumors</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>West Syndrome and Cerebral 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, 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>10</month>
<year>1989</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>08</month>
<year>2016</year>
</pub-date>
<volume>3</volume>
<issue>10</issue>
<fpage>76</fpage>
<lpage>77</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1989 The Author(s)</copyright-statement>
<copyright-year>1989</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="10.1016/0887-8994(89)90029-5" vol="5" page="327">
<article-title>Intracranial tumors and West syndrome</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Two infants, six and seven months of age, with West syndrome associated with cerebral tumors are reported from the Department of Neurology, Pediatric Hospital, Buenos Aires, Argentina.</p>
</abstract>
<kwd-group>
<kwd>Anaplastic Ependymoma</kwd>
<kwd>Ependymoma</kwd>
<kwd>Neurologic Examinations</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Two infants, six and seven months of age, with West syndrome associated with cerebral tumors are reported from the Department of Neurology, Pediatric Hospital, Buenos Aires, Argentina. Initial neurologic examinations were normal and the diagnosis of the tumors was by ultrasound and CT. One infant had a Grade III glioma in the right thalamus and the other had an anaplastic ependymoma and cyst in the right hemisphere. EEGs revealed generalized hypsarrhythmia in both cases. Infantile spasms responded to ACTH 5 IU/kg/day. One patient died at 18 months of age and the other was seizure free after complete surgical resection of the ependymoma. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p><underline>COMMENT</underline>. Other brain tumors associated with West syndrome have included choroid plexus papilloma, ganglioglioma, and optic nerve glioma. Infantile spasms and choroid plexus papilloma have also been described in Aicardi syndrome (see <underline>Ped Neurol Briefs</underline> October 1989; <underline>3</underline>:74).</p>
</disp-quote>
</body>
<back>
<ref-list>
<ref id="CIT0001">
<label>1</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Ruggieri</surname>
<given-names>V</given-names>
</name>
<name>
<surname>Caraballo</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Fejerman</surname>
<given-names>N</given-names>
</name>
</person-group>
<article-title>Intracranial tumors and West syndrome</article-title>
<source>Pediatr Neurol</source>
<year>1989</year>
<month>Sep-Oct</month>
<volume>5</volume>
<issue>5</issue>
<fpage>327</fpage>
<lpage>9</lpage>
<pub-id pub-id-type="pmid">2553029</pub-id>
<pub-id pub-id-type="doi">10.1016/0887-8994(89)90029-5</pub-id>
</element-citation>
</ref>
</ref-list>
</back>
</article>
