<?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-6-66</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-6-9-2</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Vascular 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>Moyamoya Disease: Results of Surgery</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>1992</year>
</pub-date>
<pub-date date-type="pub" publication-format="electronic">
<day>01</day>
<month>07</month>
<year>2016</year>
</pub-date>
<volume>6</volume>
<issue>9</issue>
<fpage>66</fpage>
<lpage>67</lpage>
<permissions>
<copyright-statement>Copyright: &#x00A9; 1992 The Author(s)</copyright-statement>
<copyright-year>1992</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="10.1007/BF00588191" vol="34" page="318">
<article-title>Childhood moyamoya disease before and after encephalo-duro-arterio-synangiosis: an angiographic study</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>An angiographic study of the effects of encephalo-duro-arterio-synangiosis (EDAS) in 27 children with moyamoya disease is reported from the Departments of Radiology and Neurosurgery, Tokyo Medical and Dental University, Tokyo, Japan.</p>
</abstract>
<kwd-group>
<kwd>Moyamoya Disease</kwd>
<kwd>Preoperative Angiograms</kwd>
<kwd>Hyperventilation</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>An angiographic study of the effects of encephalo-duro-arterio-synangiosis (EDAS) in 27 children with moyamoya disease is reported from the Departments of Radiology and Neurosurgery, Tokyo Medical and Dental University, Tokyo, Japan. Comparing pre- and post-operative angiograms, the development of collaterals from the external carotid arterial system into the middle cerebral artery territory was excellent in 16 of 54 cerebral hemispheres after EDAS, good in 25 and poor in 13. The development of collateral vessels from the ECA to the MCA territory increased with the severity of the stenosis of the ICA on preoperative angiograms, but in most advanced stages the development of collateral supply was less marked. The development of collateral vessels was associated with a decrease of abnormal net-like vessels. Stenosis in the ICA had progressed on 12 of the 54 cerebral hemispheres as compared with preoperative angiograms. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<disp-quote>
<p><bold>COMMENT.</bold> This study suggests that EDAS for childhood moyamoya disease should be performed as early as possible so that the development of irreversible ischaemia and permanent neurological defects may possibly be prevented.</p>
<p>Cerebral blood flow reactivity to hyperventilation in children with moyamoya disease was studied at the Department of Neurosurgery, Hokkaido University School of Medicine, Sapporo, Japan [<xref ref-type="bibr" rid="CIT0002">2</xref>]. CBF was measured by single photon emission CT (SPECT) in 11 children divided into bypass and non-bypass groups. There was some hemodynamic insufficiency in the frontal lobes of the non-bypass group who underwent procedures such as EDAS. The reduction of CBF was less after hyperventilation, especially in the frontal lobes of the bypass group in which a much better collateral blood flow occurs.</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>Yamada</surname>
<given-names>I</given-names>
</name>
<name>
<surname>Matsushima</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Suzuki</surname>
<given-names>S</given-names>
</name>
</person-group>
<article-title>Childhood moyamoya disease before and after encephalo-duro-arterio-synangiosis: an angiographic study</article-title>
<source>Neuroradiology</source>
<year>1992</year>
<volume>34</volume>
<issue>4</issue>
<fpage>318</fpage>
<lpage>322</lpage>
<pub-id pub-id-type="doi">10.1007/BF00588191</pub-id>
<pub-id pub-id-type="pmid">1528443</pub-id>
</element-citation>
</ref>
<ref id="CIT0002">
<label>2</label>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Isobe</surname>
<given-names>M</given-names>
</name>
</person-group>
<source>Neurol Surg</source>
<year>1992</year>
<month>April</month>
<volume>20</volume>
<fpage>407</fpage>
</element-citation>
</ref>
</ref-list>
</back>
</article>