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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-2014-28-5-11</article-id>
<article-id pub-id-type="doi">10.15844/pedneurbriefs-28-5-11</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Brain 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>Risk of Familial Intracranial Aneurysm</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>05</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>5</issue>
<fpage>40</fpage>
<lpage>40</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="10.1016/S1474-4422(14)70021-3" vol="13" page="385">
<article-title>Long-term, serial screening for intracranial aneurysms in individuals with a family history of aneurysmal subarachnoid hemorrhage: a cohort study</article-title>
</related-article>
<abstract abstract-type="web-summary" specific-use="electronic-only">
<p>Investigators at University Medical Center Utrecht, Netherlands, studied the yield of long-term (up to 20 years) screening for intracranial aneurysms in individuals with a positive family history (2 or more first-degree relatives) of aneurysmal subarachnoid hemorrhage (aSAH) or unruptured intracranial aneurysm (1993-2013).</p>
</abstract>
<kwd-group>
<kwd>Aneurysmal Subarachnoid Hemorrhage</kwd>
<kwd>Fusiform</kwd>
<kwd>Traumatic</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<p>Investigators at University Medical Center Utrecht, Netherlands, studied the yield of long-term (up to 20 years) screening for intracranial aneurysms in individuals with a positive family history (2 or more first-degree relatives) of aneurysmal subarachnoid hemorrhage (aSAH) or unruptured intracranial aneurysm (1993-2013). MRI or CT was performed from age 16-18 to 65-70 years. Aneurysms were identified in 51 (11%) of 458 individuals at first screening, in 21 (8%) of 261 at second screening, in 7 (5%) of 128 at third screening, and 3 (5%) of 63 at fourth screening. Five (3%) individuals with 2 negative screens had a de-novo aneurysm in follow-up screens. Smoking, history of previous aneurysm, and familial history of aneurysms were significant risk factors for aneurysms at first screening. History of previous aneurysms was the only significant risk factor for aneurysms at follow-up screening. Aneurysms were identified in 6 (5%) of 129 individuals screened before age 30 years. Long-term serial screening is advocated in individuals with a family history of aSAH. [<xref ref-type="bibr" rid="CIT0001">1</xref>]</p>
<p>COMMENTARY. Of 77 children (mean age 12 years) with 103 intracranial aneurysms treated at University California San Francisco (1981 and 2008), 25 (32%) presented with subarachnoid hemorrhage. The aneurysms were saccular in 35 (45%), fusiform in 25, traumatic in 12 patients, and infectious in 6. Treatment of 59 patients was conservative in 18. Mortality was 1.3% [<xref ref-type="bibr" rid="CIT0002">2</xref>].</p>
<p>In a long-term study of 114 pediatric patients with aneurysms at Helsinki University, Finland, the mean patient age was 14.5 years (range 3 months to 18 years) and the male:female ratio was 3:2. The most common location was the internal carotid artery bifurcation (28%). A family history of aneurysms was present in 14 (12%) [<xref ref-type="bibr" rid="CIT0003">3</xref>].</p>
</body>
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