<?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>0034-7531</journal-id>
<journal-title><![CDATA[Revista Cubana de Pediatría]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Cubana Pediatr]]></abbrev-journal-title>
<issn>0034-7531</issn>
<publisher>
<publisher-name><![CDATA[Centro Nacional de Información de Ciencias MédicasEditorial Ciencias Médicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0034-75312019000100014</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Linfangioma mesentérico en la edad pediátrica]]></article-title>
<article-title xml:lang="en"><![CDATA[Mesenteric Lynphangioma in the pediatric ages]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cabo Rodríguez]]></surname>
<given-names><![CDATA[Víctor]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Suárez Veloz]]></surname>
<given-names><![CDATA[Jhonson Sebastián]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Villa Villamar]]></surname>
<given-names><![CDATA[Saúl Guillermo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Soto Martínez]]></surname>
<given-names><![CDATA[Sonia Cecilia]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pangol Pillaga]]></surname>
<given-names><![CDATA[Andrea Stefania]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Servicio de Cirugía Pediátrica. Hospital del niño Francisco de Icaza Bustamante  ]]></institution>
<addr-line><![CDATA[Guayaquil ]]></addr-line>
<country>Ecuador</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2019</year>
</pub-date>
<volume>91</volume>
<numero>1</numero>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S0034-75312019000100014&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S0034-75312019000100014&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S0034-75312019000100014&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Introducción:  Dentro del espectro de las malformaciones congénitas con las cuales debe lidiar un cirujano pediatra, los tumores y malformaciones vasculares representan un grupo especial de entidades que continúan actualmente en estudio.  Objetivo:  Determinar las características clínicoquirúrgicas de una serie de dos casos con malformaciones de origen linfático.  Presentacion de casos:  Dos pacientes con edades pediátricas, 12 y 4 años, respectivamente, ingresaron en servicio de urgencia con signos de oclusión intestinal y lesiones tumorales quísticas abdominales que requirieron tratamiento quirúrgico con modalidades de técnicas quirúrgicas diferentes. La evolución final fue satisfactoria.  Conclusión: Los linfagiomas intestinales forman parte de la gama de presentaciones clínicas de las malformaciones de origen linfático, con una incidencia baja pero que, dada su localización y síntomas, pueden requerir tratamiento quirúrgico de urgencia. Su evolución y resolución es satisfactoria, debido al bajo índice de recidiva tras la exéresis completa.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Introduction: Within the range of congenital malfomations that surgeons have to deal with, vascular tumors and malformations represent an special group of entities that are still under study.  Objective: To determine the clinical-surgical characteristics of a series of two cases with congenital malformations of lymphatic origin.  Cases presentation: Two patients of 12 and 4 years old respectively that were admitted in the Emergencies services in the Clinical-Surgical Hospital of Guayaquil, Ecuador, with manifestations of intestinal obstruction and abdominal cystic tumoral lesions that required surgical treatments with different techniques. Final evolution was satisfactory.  Conclusion: Intestinal lymphoangiomas are part of the kinds of clinical presentations of lymphatic origin´s malformations. These have a low incidence but due to their localization and symptoms can require emergency surgical treatment. Their evolution and resolution is satisfactory due to the low index of recidive after complete exeresis.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[linfangioma mesentérico]]></kwd>
<kwd lng="es"><![CDATA[tumor quístico abdominal]]></kwd>
<kwd lng="es"><![CDATA[pediatría]]></kwd>
<kwd lng="en"><![CDATA[mesenteric lymphoangioma]]></kwd>
<kwd lng="en"><![CDATA[abdominal cystic tumor]]></kwd>
<kwd lng="en"><![CDATA[pediatrics.]]></kwd>
</kwd-group>
</article-meta>
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