<?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>0186-4866</journal-id>
<journal-title><![CDATA[Medicina interna de México]]></journal-title>
<abbrev-journal-title><![CDATA[Med. interna Méx.]]></abbrev-journal-title>
<issn>0186-4866</issn>
<publisher>
<publisher-name><![CDATA[Edición y Farmacia S.A. de C.V.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0186-48662019000400627</article-id>
<article-id pub-id-type="doi">10.24245/mim.v35i4.2476</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síndrome de Leriche]]></article-title>
<article-title xml:lang="en"><![CDATA[Leriche&#8217;s syndrome]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rozo-Ortiz]]></surname>
<given-names><![CDATA[Edwar Jassir]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vargas-Rodríguez]]></surname>
<given-names><![CDATA[Ledmar Jovanny]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Agudelo-Sanabria]]></surname>
<given-names><![CDATA[Milena Brigitte]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de Boyacá  ]]></institution>
<addr-line><![CDATA[Boyacá ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad de Boyacá  ]]></institution>
<addr-line><![CDATA[Boyacá ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2019</year>
</pub-date>
<volume>35</volume>
<numero>4</numero>
<fpage>627</fpage>
<lpage>631</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0186-48662019000400627&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0186-48662019000400627&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0186-48662019000400627&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen El síndrome de Leriche es una vasculopatía oclusiva que afecta de manera progresiva la aorta abdominal, las iliacas comunes o ambas. Se comunica el caso de una paciente con distintos factores de riesgo vascular, quien manifestó de manera aguda un cuadro clínico compatible con oclusión vascular (claudicación). Se confirmaron mediante estudio imagenológico las características de un síndrome de Leriche. La paciente finalmente falleció. La incidencia y prevalencia de este síndrome se desconocen, los casos en mujeres se asocian principalmente con enfermedades autoinmunitarias. Para el diagnóstico se requiere la realización de una adecuada historia clínica y se confirma mediante estudios imagenológicos. El tratamiento está dirigido a prevenir el avance de la enfermedad. Como parte del manejo farmacológico se encuentran algunos vasodilatadores, antiagregantes plaquetarios y las estatinas. El manejo quirúrgico puede ser cirugía a cielo abierto o endovascular, la primera demuestra mayor beneficio, a pesar de los riesgos que conlleva.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Leriche&#8217;s syndrome is an occlusive vasculopathy that progressively affects the abdominal aorta and the common iliacs. This paper reports the case of a female patient with various vascular risk factors, which presented a clinical picture compatible with vascular occlusion (claudication). The characteristics of a Leriche&#8217;s syndrome were confirmed by imaging. The patient finally died. Incidence and prevalence of Leriche&#8217;s syndrome are unknown, cases in the female gender are the main ones in autoimmune diseases. For the diagnosis, an adequate clinical history is required and confirmed by imaging studies. The treatment is aimed at preventing the progress of the disease. Within the pharmacological management are some vasodilators, antiplatelet agents and statins. Surgical management can be an open or endovascular surgery, the first one offers the greatest benefit, despite the risks involved.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Síndrome de Leriche]]></kwd>
<kwd lng="es"><![CDATA[enfermedad arterial periférica]]></kwd>
<kwd lng="es"><![CDATA[enfermedades de la aorta]]></kwd>
<kwd lng="es"><![CDATA[claudicación intermitente]]></kwd>
<kwd lng="es"><![CDATA[oclusión vascular]]></kwd>
<kwd lng="en"><![CDATA[Leriche&#8217;s syndrome]]></kwd>
<kwd lng="en"><![CDATA[peripheral arterial disease]]></kwd>
<kwd lng="en"><![CDATA[Aortic diseases]]></kwd>
<kwd lng="en"><![CDATA[intermittent claudication]]></kwd>
<kwd lng="en"><![CDATA[vascular occlusion]]></kwd>
</kwd-group>
</article-meta>
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