<?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>0120-5633</journal-id>
<journal-title><![CDATA[Revista Colombiana de Cardiología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Colomb. Cardiol.]]></abbrev-journal-title>
<issn>0120-5633</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Colombiana de Cardiologia. Oficina de Publicaciones]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0120-56332019000300159</article-id>
<article-id pub-id-type="doi">10.1016/j.rccar.2018.09.004</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Coartación aórtica abdominal en un lactante de tres meses. Tratamiento por vía endovascular]]></article-title>
<article-title xml:lang="en"><![CDATA[Coarctation of the abdominal aorta in a 3 months-old infant: Endovascular treatment]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Jiménez]]></surname>
<given-names><![CDATA[César Eduardo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Randial]]></surname>
<given-names><![CDATA[Leonardo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Robles]]></surname>
<given-names><![CDATA[Andrea]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rozo]]></surname>
<given-names><![CDATA[Juan Pablo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Universitario Clínica de San Rafael Servicio de cirugía Vascular ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital Universitario Clínica de San Rafael Servicio de Pediatría ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Hospital Militar Central  ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2019</year>
</pub-date>
<volume>26</volume>
<numero>3</numero>
<fpage>159</fpage>
<lpage>161</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0120-56332019000300159&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0120-56332019000300159&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0120-56332019000300159&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen La coartación aortica en los niños ocurre en más del 80% de casos en la aorta torácica y en muy pocos casos en la aorta abdominal, constituyendo una entidad de difícil manejo y con alta morbimortalidad. Puede ocurrir a diferentes niveles anatómicos de la aorta abdominal y con compromiso variable de las arterias viscerales, conociéndose en la literatura como síndrome aórtico medio. Se presenta el caso de un paciente de 3 meses a quien se le diagnosticó in útero la coartación aortica e hipertrofia cardiaca, con evolución hacia falla cardiaca severa, disfunción renal con requerimiento de diálisis e hipertensión arterial severa en el nacimiento. En vista de su mal estado general y edad muy temprana de presentación, se decidió manejo endovascular con angioplastia y stent aórtico, con evolución satisfactoria y mejoría clínica inmediata.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Coarctation of the abdominal aorta in infants occur, in more than 80% of cases, at thoracic aorta level, and in very cases, in the abdominal aorta. This makes it a difficult to manage condition, and with a high morbidity and mortality. It can occur at different anatomical levels of the abdominal aorta and with a variable compromise of the visceral arteries, being known in the literature as mid-aortic syndrome (MAS). The case is presented of a 3 months-old patient who was diagnosed in utero with aortic coarctation and cardiac hypertrophy, which developed into severe heart failure, kidney failure that required dialysis, and severe arterial hypertension at birth. Due to his poor general state and very young age of presentation, endovascular management was decided, with angioplasty and an aortic stent. The outcome was satisfactory and with an immediate clinical improvement.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Coartacion]]></kwd>
<kwd lng="es"><![CDATA[Endovascular]]></kwd>
<kwd lng="es"><![CDATA[Stent]]></kwd>
<kwd lng="es"><![CDATA[Hipertensión]]></kwd>
<kwd lng="en"><![CDATA[Coarctation]]></kwd>
<kwd lng="en"><![CDATA[Endovascular]]></kwd>
<kwd lng="en"><![CDATA[Stent]]></kwd>
<kwd lng="en"><![CDATA[Hypertension]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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