<?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>0300-9041</journal-id>
<journal-title><![CDATA[Ginecología y obstetricia de México]]></journal-title>
<abbrev-journal-title><![CDATA[Ginecol. obstet. Méx.]]></abbrev-journal-title>
<issn>0300-9041</issn>
<publisher>
<publisher-name><![CDATA[Federación Mexicana de Colegios de Obstetricia y Ginecología A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0300-90412018000400272</article-id>
<article-id pub-id-type="doi">10.24245/gom.v86i4.1675</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Malformación arteriovenosa uterina congénita. Presentación de un caso con hemorragia uterina masiva]]></article-title>
<article-title xml:lang="en"><![CDATA[Congenital uterine arteriovenous malformation. A case of massive uterine hemorrhage]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ávila-Vergara]]></surname>
<given-names><![CDATA[Marco Antonio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Araujo-Sánchez]]></surname>
<given-names><![CDATA[Elka Mirelle]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Zata-rain-Bayliss]]></surname>
<given-names><![CDATA[Lucía]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Camacho-Ureta]]></surname>
<given-names><![CDATA[Alejandra]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rodríguez-Angulo]]></surname>
<given-names><![CDATA[Karen]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vadillo-Ortega]]></surname>
<given-names><![CDATA[Felipe]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
<xref ref-type="aff" rid="A a"/>
<xref ref-type="aff" rid="A8"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Instituto Mexicano del Seguro Social Hospital General Regional 1 Departamento Clínico de Ginecología y Obstetricia]]></institution>
<addr-line><![CDATA[Culiacán Sinaloa]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad Autónoma de Sinaloa Facultad de Medicina ]]></institution>
<addr-line><![CDATA[Culiacán Sinaloa]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Instituto Mexicano del Seguro Social Hospital General Regional 1 Departamento Clínico de Ginecología y Obstetricia]]></institution>
<addr-line><![CDATA[Culiacán Sinaloa]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Hospital Civil de Culiacán  ]]></institution>
<addr-line><![CDATA[Culiacán Sinaloa]]></addr-line>
<country>México</country>
</aff>
<aff id="Af5">
<institution><![CDATA[,Instituto Mexicano del Seguro Social Hospital General Regional 1 ]]></institution>
<addr-line><![CDATA[Culiacán Sinaloa]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af6">
<institution><![CDATA[,Universidad Nacional Autónoma de México Instituto Nacional de Medicina Genómica Facultad de Medicina]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af7">
<institution><![CDATA[,Eunice Kennedy Shriver National Institute of Child Health and Human Development Division of Intramural Research ]]></institution>
<addr-line><![CDATA[Detroit Michigan]]></addr-line>
<country>USA</country>
</aff>
<aff id="Af8">
<institution><![CDATA[,Wayne State University School of Medicine Department of Obstetrics and Gynecology ]]></institution>
<addr-line><![CDATA[Detroit Michigan]]></addr-line>
<country>USA</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2018</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2018</year>
</pub-date>
<volume>86</volume>
<numero>4</numero>
<fpage>272</fpage>
<lpage>280</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0300-90412018000400272&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0300-90412018000400272&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0300-90412018000400272&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Antecedentes Las malformaciones arteriovenosas uterinas son raras y un diagnóstico diferencial poco considerado.  Caso clínico Paciente de 27 años que acudió a urgencias debido a hemorragia uterina abundante y abrupta, con alteración del estado hemodinámico. Antecedentes personales: malformaciones en el sistema vascular. Con base en estudios de imagen se diagnosticó una malformación arteriovenosa uterina que, por sus antecedentes, se consideró congénita. Con el propósito de disminuir los riesgos de la histerectomía y conservar la fertilidad se indicó tratamiento conservador con embolización arterial transcatéter del sistema arteriovenoso uterino afectado, con gelfoam.  Conclusiones La malformación arteriovenosa uterina es una posible causa de hemorragia uterina masiva; por tanto, debe considerarse en casos con antecedentes relevantes. Hay opciones de tratamiento que detienen la hemorragia y preservan la capacidad reproductiva. Para esto es preciso contar con un equipo multidisciplinario que identifique el sitio del defecto y aplique, de forma dirigida, la embolización arterial transcatéter de los vasos uterinos.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  BACKGROUND Uterine arteriovenous malformations are a rare condition, and the differential diagnosis is often not considered when massive uterine hemorrhage occurs.  Clinical case A case of massive uterine hemorrhage is presented in a 27- year-old woman with medical history of vascular malformations. Imaging studies diagnosed uterine arteriovenous malformation (AVM), which by her medical history was considered congenital. The patient was treated with Gelfoam uterine arterial transcatheter vascular embolization (TAE), with the purpose of reducing the risks of hysterectomy and preserving fertility.  Conclusions The uterine arteriovenous malformation is a possible cause of massive uterine hemorrhage; therefore, it should be consid ered in cases with a relevant background. There are treatment options that stop the hemorrhage and preserve the reproductive capacity. For this, it is necessary to have a multidisciplinary team that identifies the site of the defect and applies, in a targeted manner, transcatheter arterial embolization of the uterine vessels.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Malformación arteriovenosa]]></kwd>
<kwd lng="es"><![CDATA[congénita]]></kwd>
<kwd lng="es"><![CDATA[hemorragia uterina]]></kwd>
<kwd lng="es"><![CDATA[diagnóstico diferencial]]></kwd>
<kwd lng="es"><![CDATA[histerectomía]]></kwd>
<kwd lng="es"><![CDATA[sangrado uterino]]></kwd>
<kwd lng="en"><![CDATA[Congenital]]></kwd>
<kwd lng="en"><![CDATA[Arteriovenous malformation]]></kwd>
<kwd lng="en"><![CDATA[Uterine hemorrhage]]></kwd>
<kwd lng="en"><![CDATA[Differential diagnosis]]></kwd>
<kwd lng="en"><![CDATA[Hysterectomy]]></kwd>
<kwd lng="en"><![CDATA[Uterine bleeding]]></kwd>
</kwd-group>
</article-meta>
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