<?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>0028-3746</journal-id>
<journal-title><![CDATA[Neumología y cirugía de tórax]]></journal-title>
<abbrev-journal-title><![CDATA[Neumol. cir. torax]]></abbrev-journal-title>
<issn>0028-3746</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Mexicana de Neumología y Cirugía de Tórax; Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas; Sociedad Cubana de Neumología; Sociedad Paraguaya de Neumología; Sociedad Boliviana de Neumología.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0028-37462018000100034</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Malformación adenomatoidea quística, reporte de caso y revisión de la literatura]]></article-title>
<article-title xml:lang="en"><![CDATA[Cystic adenomatoid malformation, a case reports and review of the literature]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ortega-Zhindón]]></surname>
<given-names><![CDATA[Diego Bernardo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Torres-Martínez]]></surname>
<given-names><![CDATA[Rogelio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Campos-Badillo]]></surname>
<given-names><![CDATA[Adán]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital General de México &#8220;Dr. Eduardo Liceaga&#8221;  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital General &#8220;Dr. Gustavo Baz Prada&#8221;  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2018</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2018</year>
</pub-date>
<volume>77</volume>
<numero>1</numero>
<fpage>34</fpage>
<lpage>37</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0028-37462018000100034&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0028-37462018000100034&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0028-37462018000100034&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen: La malformación adenomatoidea quística es una anormalidad rara del tracto respiratorio inferior, con alteración del desarrollo de estructuras endodérmicas y mesodérmicas, representando la coexistencia de cavidades quísticas con estructuras secretorias adenomatosas propias del aparato respiratorio. Los pacientes afectados pueden presentar dificultad respiratoria en el período perinatal o de forma tardía, que gracias a las nuevas técnicas de imagen nos permite un mejor acercamiento al diagnóstico y con esto a una resolución terapéutica oportuna. Presentamos el caso de un neonato que se resolvió a través del tratamiento quirúrgico, con un resultado exitoso y actualmente con buena evolución y pronóstico.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract: Cystic adenomatoid malformation is a rare abnormality of the lower respiratory tract, with altered development of endodermal and mesodermal structures, describes the coexistence of cystic cavities with adenomatous secretory structures, characteristic of the respiratory system. Affected patients may present respiratory distress in the perinatal, or late, period that thanks to the new imaging techniques allows us a better approach to the diagnosis and with this to a timely therapeutic resolution. We present the case of a neonate who was resolved through surgical treatment, with a successful outcome and currently with good evolution and prognosis.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Desarrollo alveolar]]></kwd>
<kwd lng="es"><![CDATA[diagnóstico prenatal]]></kwd>
<kwd lng="es"><![CDATA[malformación adenomatoidea quística]]></kwd>
<kwd lng="en"><![CDATA[Alveolar development]]></kwd>
<kwd lng="en"><![CDATA[cystic adenomatoid malformation]]></kwd>
<kwd lng="en"><![CDATA[prenatal diagnosis]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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