<?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>1012-2966</journal-id>
<journal-title><![CDATA[Gaceta Médica Boliviana]]></journal-title>
<abbrev-journal-title><![CDATA[Gac Med Bol]]></abbrev-journal-title>
<issn>1012-2966</issn>
<publisher>
<publisher-name><![CDATA[Facultad de Medicina de la Universidad Mayor de San Simón]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1012-29662021000200240</article-id>
<article-id pub-id-type="doi">10.47993/gmb.v44i2.284</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Tumor de Células de Sertoli Esclerosante Testicular]]></article-title>
<article-title xml:lang="en"><![CDATA[Sclerosing Sertoli cell tumor of the testis]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vargas-Rocha]]></surname>
<given-names><![CDATA[Vladimir Erik]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Segales-Rojas]]></surname>
<given-names><![CDATA[Patricia]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vargas Rocha]]></surname>
<given-names><![CDATA[Brian E.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Caja Nacional de Salud Hospital Obrero N° 2 ]]></institution>
<addr-line><![CDATA[Cochabamba ]]></addr-line>
<country>Bolivia</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Instituto Gastroenterológico Boliviano Japonés  ]]></institution>
<addr-line><![CDATA[Cochabamba ]]></addr-line>
<country>Bolivia</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,UMSS  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2021</year>
</pub-date>
<volume>44</volume>
<numero>2</numero>
<fpage>240</fpage>
<lpage>243</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.bo/scielo.php?script=sci_arttext&amp;pid=S1012-29662021000200240&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.bo/scielo.php?script=sci_abstract&amp;pid=S1012-29662021000200240&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.bo/scielo.php?script=sci_pdf&amp;pid=S1012-29662021000200240&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen Actualmente el tumor de células de Sertoli de tipo esclerosante, se encuentra clasificado como una variante de los tumores de células de Sertoli NOS (sin otra especificación), ya que ambos tumores presentan mutación del gen CTNNB1, codificador de b-catenina, la relevancia de su identificación radica en que esta variante se correlaciona, aunque en un bajo porcentaje, con potencial metastásico.Masculino de 56 años de edad, con cuadro de 7 años de evolución, caracterizado por presentar dolor testicular izquierdo con leve aumento de consistencia en polo inferior de testículo izquierdo, se realiza ecografía testicular, en la que se evidencia lesión heterogénea de 2 cm de diámetro máximo, dependiente de polo inferior de testículo izquierdo; se realiza orquiectomía radical izquierda, con reporte histopatológico: tumor de células de sertoli testicular. Cursando posteriormente con evolución satisfactoria, con cicatrización completa de la herida, y actualmente en vigilancia, sin necesidad de tratamiento adyuvante. Conociendo su relativa rareza y los pocos casos notificados, los tumores testiculares de células de Sertoli siguen siendo un misterio relativo y en la actualidad, continúan siendo un desafío para su diagnóstico. Con este caso, pretendemos apoyar en el conocimiento y fomentar la investigación adicional de estos tumores, con el objetivo de optimizar el diagnóstico, dar un adecuado tratamiento.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Currently, the sclerosing-type Sertoli cell tumor is classified as a variant of the NOS Sertoli cell tumors (without other specification), because it has been shown that both tumors present mutation in the CTNNB1 gene, which encodes the b-catenin (19), the relevance of its identification lies in the fact that this variant is correlated, although in a low percentage, with metastatic potential. A 56-year-old male, with a 7-year evolution, characterized by presenting left testicular pain with a slight increase in consistency in the lower pole of the left testicle, a testicular ultrasound was performed, which revealed a heterogeneous lesion of 2 cm in diameter maximum, dependent on the lower pole of the left testis; Left radical orchiectomy was performed, with histopathological report: testicular sertoli cell tumor. Later, with satisfactory evolution, with complete wound healing, and currently under surveillance, without the need for adjuvant treatment.Knowing their relative rarity and the few reported cases, testicular Sertoli cell tumors remain a relative mystery and today, they continue to be a challenge for diagnosis. With this case, we intend to support the knowledge and promote additional research on these tumors, with the aim of optimizing the diagnosis and providing adequate treatment.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[tumor]]></kwd>
<kwd lng="es"><![CDATA[células de sertoli]]></kwd>
<kwd lng="es"><![CDATA[testículo]]></kwd>
<kwd lng="en"><![CDATA[tumor]]></kwd>
<kwd lng="en"><![CDATA[sertoli cells]]></kwd>
<kwd lng="en"><![CDATA[testis]]></kwd>
</kwd-group>
</article-meta>
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