<?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>1727-897X</journal-id>
<journal-title><![CDATA[MediSur]]></journal-title>
<abbrev-journal-title><![CDATA[Medisur]]></abbrev-journal-title>
<issn>1727-897X</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Ciencias Médicas de Cienfuegos, Centro Provincial de Ciencias Médicas, Provincia de Cienfuegos.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1727-897X2021000400682</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Feocromocitoma Benigno vs Tumor Renal. Presentación de un caso]]></article-title>
<article-title xml:lang="en"><![CDATA[Benign Pheochromocytoma vs Kidney Tumor. A case presentation]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rodríguez Cruzata.]]></surname>
<given-names><![CDATA[Lesyibeth]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Santiesteban Bello.]]></surname>
<given-names><![CDATA[Aida Nelis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gonzáles Garrido.]]></surname>
<given-names><![CDATA[Mercedes]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital General Docente Orlando Pantoja Tamayo  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2021</year>
</pub-date>
<volume>19</volume>
<numero>4</numero>
<fpage>682</fpage>
<lpage>689</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S1727-897X2021000400682&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S1727-897X2021000400682&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S1727-897X2021000400682&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN  Introducción:  El feocromocitoma es una neoplasia neuroendocrina localizada en la médula adrenal.  Objetivo:  Destacar la importancia que todavía posee en la práctica clínica el interrogatorio y el examen físico minucioso, a pesar de los novedosos medios diagnósticos con que se cuenta en la actualidad.  Presentación del caso : Se presenta caso clínico de paciente masculino de 17 años de edad, con incidentaloma suprarrenal izquierdo, catalogado inicialmente como tumor renal abscedado, cuya biopsia de pieza operatoria demostró finalmente que correspondía a un feocromocitoma benigno. La determinación de catecolaminas fue normal, en la tomografía computarizada se evidenció una masa retroperitoneal que involucraba riñón y suprarrenal izquierdos. Se realizó la resección de la neoplasia y fue dado de alta médica en buenas condiciones.  Conclusiones:  El feocromocitoma es una patología infrecuente y compleja, cuya resolución quirúrgica es mandatoria.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Background:  Pheochromocytoma is a neuroendocrine neoplasm located in the adrenal medulla.  Objective:  To highlight the importance of physical examination and the detailed clinical practice, despite the new diagnostic means that are currently available.  Case presentation:  A 17-years-old male patient with left adrenal incidentaloma, initially classified as an abscessed renal tumor, whose surgical specimen biopsy finally showed that it corresponded to a benign pheochromocytoma it is presented. The catecholamine determination was normal, the computed tomography revealed a retroperitoneal mass that involved the left kidney and adrenal. The neoplasm was resected and he was discharged in good condition.  Conclusions: Pheochromocytoma is an infrequent and complex pathology, whose surgical resolution is necessary.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Feocromocitoma]]></kwd>
<kwd lng="es"><![CDATA[enfermedad]]></kwd>
<kwd lng="es"><![CDATA[presentacion de caso.]]></kwd>
<kwd lng="en"><![CDATA[Phecromocytoma]]></kwd>
<kwd lng="en"><![CDATA[disease]]></kwd>
<kwd lng="en"><![CDATA[case presentation]]></kwd>
</kwd-group>
</article-meta>
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