<?xml version="1.0" encoding="ISO-8859-1"?><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">
<front>
<journal-meta>
<journal-id>2631-2581</journal-id>
<journal-title><![CDATA[Revista Ecuatoriana de Neurología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Ecuat Neurol]]></abbrev-journal-title>
<issn>2631-2581</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Médica Ecuatoriana de Neurología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2631-25812017000200283</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Tumores de Sistema Nervioso Central en Pediatría: Presente y Futuro del Abordaje Diagnóstico]]></article-title>
<article-title xml:lang="en"><![CDATA[Central nervous system tumors in pediatrics: present and future of diagnostic approach]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Toro-Moreno]]></surname>
<given-names><![CDATA[Ana Cristina]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Serna-Velez]]></surname>
<given-names><![CDATA[Laura]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gallego-González]]></surname>
<given-names><![CDATA[Daniel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Jaramillo-Jaramillo]]></surname>
<given-names><![CDATA[Laura Isabel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Martínez-Sánchez]]></surname>
<given-names><![CDATA[Lina María]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Álvarez-Hernández]]></surname>
<given-names><![CDATA[Luis Felipe]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Pontificia Bolivariana Escuela de Ciencias de la Salud Facultad de Medicina]]></institution>
<addr-line><![CDATA[Medellín ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2017</year>
</pub-date>
<volume>26</volume>
<numero>3</numero>
<fpage>283</fpage>
<lpage>288</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.senescyt.gob.ec/scielo.php?script=sci_arttext&amp;pid=S2631-25812017000200283&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.senescyt.gob.ec/scielo.php?script=sci_abstract&amp;pid=S2631-25812017000200283&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.senescyt.gob.ec/scielo.php?script=sci_pdf&amp;pid=S2631-25812017000200283&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Los tumores de sistema nervioso central son neoplasias con alta frecuencia durante la infancia, con una incidencia que alcanza los 31,2 casos por millón de niños, siendo el más común de estos el astrocitoma. Estos son producto de una combinación de factores genéticos y epigenéticos que determinan no solo su aparición, sino también, el comportamiento y pronóstico del mismo. La presentación clínica de estas neoplasias va desde súbita y clara, hasta larvada y ambigua, en ocasiones, dificultando realizar un adecuado abordaje y un diagnóstico precoz, por lo cual se han destinado muchos recursos para la evaluación y estandarización de nuevos métodos diagnósticos como lo son los marcadores tumorales. Objetivo: Ofrecer una revisión clara acerca de los tumores de sistema nervioso central y nuevas perspectivas en el diagnóstico.  Se llevó a cabo una búsqueda de literatura en bases de datos empleando los descriptores sistema nervioso central, neoplasias, astrocitoma, se incluyeron 25 artículos en español y en inglés.  Los tumores de sistema nervioso central cobran una relevancia notable en la población pediátrica, su comportamiento y pronóstico hacen necesaria la búsqueda de nuevas ayudas que permitan un diagnóstico precoz.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Central nervous system tumors are neoplasms with high frequency during childhood, with an incidence of 31,2 cases per million children, the most common being astrocytoma. These are the product of a combination of genetic and epigenetic factors that determine not only their appearance, but also their behavior and prognosis. The clinical presentation of these neoplasms ranges from the sudden and clear, to the gradual and ambiguous, which represents a barrier to carrying out an adequate approach and an early diagnosis. That is the reason to destinate many resources for evaluation and standarization of new diagnostic methods like tumor markers. Objective: To provide a clear review of central nervous system tumors and new perspectives in diagnosis.  A search of the literature was carried out in databases using the descriptors central nervous system, neoplasms, astrocytoma. 25 articles were included in spanish and english.  Central nervous system tumors have a significant relevance in the pediatric population. Their behavior and prognosis necessitate searching for new aids for an early diagnosis.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Sistema nervioso central]]></kwd>
<kwd lng="es"><![CDATA[neoplasias]]></kwd>
<kwd lng="es"><![CDATA[astrocitoma]]></kwd>
<kwd lng="en"><![CDATA[Central nervous system]]></kwd>
<kwd lng="en"><![CDATA[neoplasms]]></kwd>
<kwd lng="en"><![CDATA[astrocytoma]]></kwd>
</kwd-group>
</article-meta>
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