<?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>2444-6483</journal-id>
<journal-title><![CDATA[Endoscopia]]></journal-title>
<abbrev-journal-title><![CDATA[Endoscopia]]></abbrev-journal-title>
<issn>2444-6483</issn>
<publisher>
<publisher-name><![CDATA[Asociación Mexicana de Endoscopia Gastrointestinal A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2444-64832021000200084</article-id>
<article-id pub-id-type="doi">10.24875/end.21000022</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síndrome Osler-Weber-Rendu. Manejo endoscópico de un sangrado inusual: reporte de caso]]></article-title>
<article-title xml:lang="en"><![CDATA[Osler-Weber-Rendu. Endoscopic management of an unusual bleeding: case report]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cherem-Kibrit]]></surname>
<given-names><![CDATA[Marcos]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gomes da Silva-de Rosenzweig]]></surname>
<given-names><![CDATA[Pablo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vega-González]]></surname>
<given-names><![CDATA[Francisco de la]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gutiérrez-Alvarado]]></surname>
<given-names><![CDATA[Rubén]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Govea-González]]></surname>
<given-names><![CDATA[Óscar]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Garduño-Hernández]]></surname>
<given-names><![CDATA[Isaías]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ramírez-Amezcua]]></surname>
<given-names><![CDATA[Francisco J.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Anáhuac Facultad de Ciencias de la Salud ]]></institution>
<addr-line><![CDATA[Huixquilucan Edo. Méx]]></addr-line>
<country>Méx</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Centro Médico ABC Servicio de Endoscopia Departamento de Cirugía]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Hospital Regional ISSSTE Lic. Adolfo López Mateos Servicio de Endoscopia Departamento de Cirugía]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Hospital General ISSSTE Dr. Darío Fernández Fierro Servicio de Endoscopia Departamento de Cirugía]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2021</year>
</pub-date>
<volume>33</volume>
<numero>2</numero>
<fpage>84</fpage>
<lpage>86</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S2444-64832021000200084&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S2444-64832021000200084&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S2444-64832021000200084&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen El síndrome de Osler-Weber-Rendu (OWR), también llamado telangiectasia hemorrágica hereditaria, es un trastorno vascular hereditario que se transmite de manera autosómica dominante con una incidencia de 1 por cada 8,000-16,500 habitantes. Las recomendaciones actuales para el tratamiento de la hemorragia gastrointestinal por OWR incluyen el uso de estrógenos-progestágenos y el tratamiento endoscópico con argón plasma. Se presenta el caso de un hombre de 69 años con diagnóstico de OWR que recibe manejo endoscópico exitoso.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Osler-Weber-Rendu syndrome (OWR), also called Hereditary hemorrhagic telangiectasia (HHT) is a hereditary vascular disorder that is transmitted as an autosomal dominant trait, with an incidence of 1 per 8,000-16,500 inhabitants. Current recommendations for the treatment of gastrointestinal bleeding from OWR include the use of estrogen-progestogens and endoscopic treatment with argon plasma. We present the case of a 69-year-old man diagnosed with OWR who receives successful endoscopic management.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Endoscopia]]></kwd>
<kwd lng="es"><![CDATA[Telangiectasia]]></kwd>
<kwd lng="es"><![CDATA[Hemorragia]]></kwd>
<kwd lng="en"><![CDATA[Endoscopy]]></kwd>
<kwd lng="en"><![CDATA[Telangiectasia]]></kwd>
<kwd lng="en"><![CDATA[Hemorrhage]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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