<?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>1405-0099</journal-id>
<journal-title><![CDATA[Cirujano general]]></journal-title>
<abbrev-journal-title><![CDATA[Cir. gen]]></abbrev-journal-title>
<issn>1405-0099</issn>
<publisher>
<publisher-name><![CDATA[Asociación Mexicana de Cirugía General A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1405-00992017000100013</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Neoplasias quísticas de páncreas: una causa más de dolor abdominal inespecífico. Experiencia terapéutica de 10 años en la Unidad de Cirugía Hepato-Pancreato-Biliar del Hospital General de México]]></article-title>
<article-title xml:lang="en"><![CDATA[Cystic pancreatic neoplasms: one more cause of nonspecific abdominal pain. Ten-year therapeutic experience in the Hepato-Pancreato-Biliary Surgery Unit of the General Hospital of Mexico]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Chapa Azuela]]></surname>
<given-names><![CDATA[Óscar]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gopar Ochoa]]></surname>
<given-names><![CDATA[Clara Verónica]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Etchegaray Dondé]]></surname>
<given-names><![CDATA[Agustín]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Higuera Hidalgo]]></surname>
<given-names><![CDATA[Francisco]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ortiz Higareda]]></surname>
<given-names><![CDATA[Vanessa]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital General de México Servicio de la Clínica de Páncreas ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado Hospital Darío Fernández ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Hospital General de México  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Instituto Mexicano del Seguro Social Centro Médico Nacional &#8220;Siglo XXI&#8221; servicio de cirugía general]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2017</year>
</pub-date>
<volume>39</volume>
<numero>1</numero>
<fpage>13</fpage>
<lpage>18</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1405-00992017000100013&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1405-00992017000100013&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1405-00992017000100013&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen:  Introducción:  Las neoplasias quísticas de páncreas (NQP) se originan a partir de los diversos componentes glandulares; son lesiones infrecuentes que se manifiestan como dolor abdominal crónico e inespecífico. Son subdiagnosticadas. Su conocimiento debe ser difundido con base en que cada estirpe histológica presenta comportamiento biológico distinto y puede progresar a carcinoma invasivo; su diagnóstico y terapéutica en etapas tempranas es fundamental. En el Hospital General de México se llevó a cabo un análisis retrospectivo de los pacientes con NQP tratados en la clínica de patología hepatobiliar.  Material y métodos:  Se realizó un estudio retrospectivo, descriptivo y transversal de enero de 2004 a diciembre de 2014 en el que se analizaron las características demográficas y clínicas de los pacientes con diagnóstico de NQP que fueron tratados mediante resección quirúrgica; los resultados fueron expresados mediante medidas de tendencia central y porcentajes.  Resultados:  Se incluyó un total de 18 casos, todos del sexo femenino, con una frecuencia de dos casos por año y una edad promedio de 38 años; la cirugía realizada con mayor frecuencia fue la pancreatectomía distal y en segundo lugar, la pancreatoduodenectomía, con una morbilidad del 39% y una mortalidad del 6%. Los diagnósticos histopatológicos fueron neoplasia quística mucinosa (NQM) 33%, neoplasia sólido quística pseudopapilar mucinosa (NSQPM) 33%, neoplasia quística serosa (NQS) 22%, carcinoma neuroendocrino con degeneración quística (CNQ) 6%, quiste linfoepitelial (QL) 6%. La supervivencia global a cinco años fue del 83%.  Discusión:  Las NQP constituyen un reto diagnóstico y terapéutico. En nuestro medio, el tratamiento quirúrgico fue curativo en el 83% de los casos. El abordaje de los pacientes con NQP debe llevarse a cabo en unidades especializadas en patología hepatobiliar, ya que favorece mejores resultados.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract:  Introduction:  Pancreatic cystic neoplasms (PCN) originate from various glandular components; these are infrequent lesions that manifest as chronic and non-specific abdominal pain and are under diagnosed. Their knowledge must be diffused on the basis that each histological strain presents different biological behavior and it progresses to invasive carcinoma; its diagnosis and therapeutics in the early stages are critical. A retrospective analysis of patients with PCN treated at the hepatobiliary pathology clinic was carried out at the General Hospital of Mexico.  Material and methods:  A retrospective, descriptive and cross-sectional study was carried out from January 2004 to December 2014, in which we analyzed the demographic and clinical characteristics of the patients with a diagnosis of PCN, who were treated by surgical resection; the results were expressed through measures of central tendency and percentages.  Results:  A total of 18 cases, all of them female, with a frequency of two cases per year and a mean age of 38 years. The most frequently performed surgery was distal pancreatectomy and, secondly, pancreatoduodenectomy, with a morbidity of 39% and a mortality of 6%. Histopathological diagnoses were mucinous cystic neoplasm 33%, solid cystic neoplasm pseudopapillary mucinous 33%, serous cystic neoplasm 22%, neuroendocrine carcinoma with cystic degeneration 6%, and lymphoepithelial cyst 6%. Overall survival at five years was 83%.  Discussion:  PCN is a diagnostic and therapeutic challenge. In our setting, surgical treatment was curative in 83% of cases. The care of patients with PCN should be carried out in specialized units in hepatobiliary pathology, since it favors better results.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Páncreas]]></kwd>
<kwd lng="es"><![CDATA[neoplasias quísticas]]></kwd>
<kwd lng="es"><![CDATA[carcinoma quístico]]></kwd>
<kwd lng="es"><![CDATA[dolor abdominal]]></kwd>
<kwd lng="en"><![CDATA[Pancreas]]></kwd>
<kwd lng="en"><![CDATA[cystic neoplasms]]></kwd>
<kwd lng="en"><![CDATA[cystic carcinoma]]></kwd>
<kwd lng="en"><![CDATA[abdominal pain]]></kwd>
</kwd-group>
</article-meta>
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