<?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>2007-4085</journal-id>
<journal-title><![CDATA[Revista mexicana de urología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. mex. urol.]]></abbrev-journal-title>
<issn>2007-4085</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Mexicana de Urología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2007-40852021000500004</article-id>
<article-id pub-id-type="doi">10.48193/revistamexicanadeurologa.v81i5.706</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Duplicación uretral incompleta. Reporte de un caso y revisión de la literatura]]></article-title>
<article-title xml:lang="en"><![CDATA[Incomplete urethral duplication. Case report and literature review]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mendoza-Sánchez]]></surname>
<given-names><![CDATA[Leonardo José]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Calviac-Mendoza]]></surname>
<given-names><![CDATA[Rosario]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Guerra-Rodríguez]]></surname>
<given-names><![CDATA[Marlene]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Nápoles-Rivera]]></surname>
<given-names><![CDATA[Jorge Antonio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de Ciencias Médicas de La Habana  ]]></institution>
<addr-line><![CDATA[La Habana ]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>10</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>10</month>
<year>2021</year>
</pub-date>
<volume>81</volume>
<numero>5</numero>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S2007-40852021000500004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S2007-40852021000500004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S2007-40852021000500004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Descripción del caso:  Masculino de 3 años de edad que consulta por episodios de disuria y salida de orina por región perineal posterior a la micción fisiológica, a la exploración física se encuentra pápula enrojecida en región perineal, motivo por lo que se realiza uretrocistografía miccional diagnosticando duplicación uretral tipo IIa-2 de Effman y se decide realizar extirpación completa del trayecto accesorio.  Relevancia:  La duplicación uretral es una entidad congénita inusual, con my pocos casos reportados en la literatura, incluso descrita solo por los reparos anatómicos y suele asociarse a otras malformaciones gastrointestinales y genitourinarias.  Implicaciones clínicas:  El diagnóstico se realiza generalmente en la infancia mediante uretrocistografía miccional, urografía retrógrada y cistouretroscopía, el tratamiento se reserva para pacientes sintomáticos, en este caso se realizo extirpación completa del trayecto accesorio, con evolución satisfactoria.  Conclusiones:  La duplicación uretral es una entidad rara, diagnosticada en la infancia, que se puede asociar a otras malformaciones. La uretrocistografía miccional permite hacer el diagnóstico. La extirpación del trayecto accesorio fue el tratamiento indicado con evolución favorable.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Description of the case:  3-year-old male who consulted for episodes of dysuria and urine leakage from the perineal region after physiological urination, on physical examination a reddened papule was found in the perineal region, which is why a voiding urethrocystography was performed diagnosing Effman's type IIa-2 urethral duplication and it was decided to perform complete removal of the accessory tract.  Relevance:  Urethral duplication is an unusual congenital entity, with very few cases reported in the literature, even described only due to anatomical concerns and is usually associated with other gastrointestinal and genitourinary malformations.  Clinical implications:  urethral duplication is a rare entity, diagnosed in childhood, which can be associated with other malformations. Voiding urethrocystography allows the diagnosis to be made. Removal of the accessory tract was the indicated treatment with a favorable outcome.  Conclusions:  urethral duplication is a rare entity, diagnosed in childhood, associated with other malformations. Voiding urethrocystography allows the diagnosis to be made. Removal of the accessory tract was the indicated treatment with a favorable outcome.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Urethral duplication]]></kwd>
<kwd lng="en"><![CDATA[congenital aberration]]></kwd>
<kwd lng="en"><![CDATA[diagnosis and treatment]]></kwd>
<kwd lng="es"><![CDATA[Duplicación uretral]]></kwd>
<kwd lng="es"><![CDATA[anomalía congénita]]></kwd>
<kwd lng="es"><![CDATA[diagnóstico y tratamiento]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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