<?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>S2007-40852024000100004</article-id>
<article-id pub-id-type="doi">10.48193/y4nnwq31</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Revisión sistemática del síndrome de Zinner]]></article-title>
<article-title xml:lang="en"><![CDATA[Systematic review of Zinner syndrome]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Palacios-Rosas]]></surname>
<given-names><![CDATA[Erika]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Torres-Razo]]></surname>
<given-names><![CDATA[Andrea]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Enríquez-González]]></surname>
<given-names><![CDATA[Enrique Alonso]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de las Américas  ]]></institution>
<addr-line><![CDATA[ Puebla]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>02</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>02</month>
<year>2024</year>
</pub-date>
<volume>84</volume>
<numero>1</numero>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S2007-40852024000100004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S2007-40852024000100004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S2007-40852024000100004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen El síndrome de Zinner se caracteriza por ser una patología de origen congénito en la cual se observa una ausencia unilateral del riñón, presencia de quistes y obstrucción en los conductos eyaculatorios. Al ser diagnosticada en la etapa de actividad sexual de los pacientes, puede causar problemas en la sexualidad o en la reproductividad de la persona. Este trabajo tuvo como objetivo realizar una revisión sistemática de casos clínicos reportados en la literatura entre el año 2013 a 2023. Se evaluaron 42 reportes de casos clínicos con dicho síndrome, con un total de 49 pacientes con una media de edad de 22.5 años, el 77.55 % de los pacientes presentaron quistes, ausencia del riñón derecho en el 44.90% de los pacientes, y el 91.84 % presentaron dolor. El tratamiento más común para esta patología es la laparoscopia (16.33 %) y en los casos revisados no se presentaron complicaciones ni decesos. El identificar las diferentes presentaciones de este síndrome podría mejorar la rapidez del diagnóstico, y garantizar un manejo efectivo, mejorando con ello la calidad de vida de los pacientes.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Zinner syndrome is characterized as a pathology of congenital origin in which there is a unilateral absence of the kidney, presence of cysts and obstruction in the ejaculatory ducts. Being diagnosed in the stage of sexual activity of patients, it can cause problems in the person's sexuality or reproduction. The objective of this work was to carry out a systematic review of clinical cases reported in the literature between 2013 and 2023. 42 reports of clinical cases with Zinner syndrome were evaluated, with a total of 49 patients with a mean age of 22.5 years, the 77.55 % of the patients presented cysts, absence of the right kidney in 44.90 % of the patients, and 91.84 % presented pain. The most common treatment for this pathology was laparoscopy (16.33 %) and in the reviewed cases there were no complications or deaths. Identifying the different presentations of this syndrome could improve the speed of diagnosis and guarantee effective management, thereby improving the quality of life of patients.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Zinner syndrome]]></kwd>
<kwd lng="en"><![CDATA[congenital abnormalities]]></kwd>
<kwd lng="en"><![CDATA[seminal vesicles]]></kwd>
<kwd lng="en"><![CDATA[unilateral renal agenesis]]></kwd>
<kwd lng="es"><![CDATA[Síndrome de Zinner]]></kwd>
<kwd lng="es"><![CDATA[anomalías congénitas]]></kwd>
<kwd lng="es"><![CDATA[vesículas seminales]]></kwd>
<kwd lng="es"><![CDATA[agenesia renal unilateral]]></kwd>
</kwd-group>
</article-meta>
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<page-range>71-3</page-range></nlm-citation>
</ref>
<ref id="B40">
<label>40</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Razdan]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Kryvenko]]></surname>
<given-names><![CDATA[ON]]></given-names>
</name>
<name>
<surname><![CDATA[Razdan]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Robotic-assisted laparoscopic vesiculectomy in a patient with atypical Zinner syndrome presenting with large cyst involving bilateral seminal vesicles and vasa deferentia]]></article-title>
<source><![CDATA[Urology Case Reports]]></source>
<year>2018</year>
<volume>18</volume>
<page-range>79-81</page-range></nlm-citation>
</ref>
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</back>
</article>
