<?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>2307-0420</journal-id>
<journal-title><![CDATA[Cirugía paraguaya]]></journal-title>
<abbrev-journal-title><![CDATA[Cir. parag.]]></abbrev-journal-title>
<issn>2307-0420</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Paraguaya de Cirugía]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2307-04202020000100028</article-id>
<article-id pub-id-type="doi">10.18004/sopaci.2020.abril.28-29</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Esplenopancreatectomia corporocaudal videoasistida por tumor de Frantz]]></article-title>
<article-title xml:lang="en"><![CDATA[Splenopancreatectomy corporocaudal video-assisted tumor Frantz]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Duarte]]></surname>
<given-names><![CDATA[Dayhana]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Delgado]]></surname>
<given-names><![CDATA[Marcos]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Feltes]]></surname>
<given-names><![CDATA[Soel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Kostinchok]]></surname>
<given-names><![CDATA[Michel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ferreira]]></surname>
<given-names><![CDATA[Miguel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Nacional de Itauguá Servicio de Cirugía General ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Paraguay</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>04</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>04</month>
<year>2020</year>
</pub-date>
<volume>44</volume>
<numero>1</numero>
<fpage>28</fpage>
<lpage>29</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.iics.una.py/scielo.php?script=sci_arttext&amp;pid=S2307-04202020000100028&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.iics.una.py/scielo.php?script=sci_abstract&amp;pid=S2307-04202020000100028&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.iics.una.py/scielo.php?script=sci_pdf&amp;pid=S2307-04202020000100028&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN El tumor pseudopapilar sólido del páncreas es poco frecuente de bajo potencial maligno. Se presenta el caso de una mujer de 17 años de edad acude a consulta por dolor abdominal de inicio insidioso de moderada intensidad; sin hallazgossignificativos en el examen físico; la ecografía abdominal informa imagen nodular sólida de 8x6 cm en cuerpo y cola de páncreas con señal vascular central y periférica al Doppler color, se realiza tomografía con contraste de abdomen en donde se evidencia gran tumoración que abarca cuerpo y cola del páncreas aproximadamente 10x8cm con proyección al hilio esplénico. La resección de la masa y el examen histopatológico confirmaron el diagnóstico de tumor pseudopapilar del páncreas. Conclusión: la neoplasia pseudopapilar del páncreas es una condición rara, que requiere intervención quirúrgica. Es necesario un seguimiento minucioso para la detección temprana de la recurrencia y metástasis.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT Solid pseudopapillary tumor of the pancreas is uncommon with low malignant potential. The case of a 17-year-old woman is presented for consultation due to insidious abdominal pain of moderate intensity; no significant findings on the physical exam; Abdominal ultrasound reports a solid nodular image of 8x6 cm in the body and tail of the pancreas with a central and peripheral vascular signal to the color Doppler. A contrast-enhanced tomography is performed, showing a large tumor that covers the body and tail of the pancreas approximately 10x8cm with projection, to splenic hilum. Mass resection and histopathological examination confirmed the diagnosis of pseudopapillary tumor of the pancreas. Conclusion: Pseudopapillary neoplasm of the pancreas is a rare condition, which requires surgical intervention. Careful monitoring is necessary for the early detection of recurrence and metastasis.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[páncreas]]></kwd>
<kwd lng="es"><![CDATA[tumor]]></kwd>
<kwd lng="es"><![CDATA[pseudopapilar]]></kwd>
<kwd lng="es"><![CDATA[dolor]]></kwd>
<kwd lng="en"><![CDATA[pancreas]]></kwd>
<kwd lng="en"><![CDATA[tumor]]></kwd>
<kwd lng="en"><![CDATA[pseudopapillary]]></kwd>
<kwd lng="en"><![CDATA[pain]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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