<?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>1817-7433</journal-id>
<journal-title><![CDATA[Revista Científica Ciencia Médica]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Cient Cienc Méd]]></abbrev-journal-title>
<issn>1817-7433</issn>
<publisher>
<publisher-name><![CDATA[Facultad de Medicina, Universidad Mayor de San Simón.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1817-74332021000100078</article-id>
<article-id pub-id-type="doi">10.51581/rccm.v24i1.348</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[AGENESIA PULMONAR COMO HALLAZGO INFRECUENTE EN ADULTOS: REPORTE DE CASO]]></article-title>
<article-title xml:lang="en"><![CDATA[PULMONARY AGENESIS AS A RARE FINDING IN ADULTS: CASE REPORT]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gradis Santos]]></surname>
<given-names><![CDATA[Olman Daniel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Degrandes Rodríguez]]></surname>
<given-names><![CDATA[Bayron Josué]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Aguilera Tercero]]></surname>
<given-names><![CDATA[Lucy Gabriela]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gutiérrez Villanueva]]></surname>
<given-names><![CDATA[Semma Julissa]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Católica de Honduras  ]]></institution>
<addr-line><![CDATA[Tegucigalpa ]]></addr-line>
<country>Honduras</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Instituto Nacional Cardiopulmonar  ]]></institution>
<addr-line><![CDATA[Tegucigalpa ]]></addr-line>
<country>Honduras</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Universidad Católica de Honduras  ]]></institution>
<addr-line><![CDATA[Tegucigalpa ]]></addr-line>
<country>Honduras</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2021</year>
</pub-date>
<volume>24</volume>
<numero>1</numero>
<fpage>78</fpage>
<lpage>81</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.bo/scielo.php?script=sci_arttext&amp;pid=S1817-74332021000100078&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.bo/scielo.php?script=sci_abstract&amp;pid=S1817-74332021000100078&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.bo/scielo.php?script=sci_pdf&amp;pid=S1817-74332021000100078&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN La agenesia pulmonar es una malformación infrecuente que se caracteriza por la ausencia de uno o ambos parénquimas pulmonares, estructuras bronquiales y vasculares. Posee una incidencia de un caso por cada 10 000 a 15 000 nacidos vivos. Generalmente, el diagnóstico es realizado durante la niñez, aunque puede llegar a presentarse asintomático hasta la edad adulta, lo cual su diagnóstico resulta un hallazgo incidental durante exámenes de rutina. Habiendo pocos casos descritos. Reportamos el caso de una paciente femenina 40 años de edad, quien fue referida al servicio de emergencia de nuestro &#8220;Hospital del Tórax&#8221; por presentar dolor torácico, disnea de medianos esfuerzos y fiebre de un mes de evolución.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT Pulmonary agenesis is a rare malformation characterized by the absence of one or both pulmonary parenchyma, bronchial and vascular structures. Has an incidence of one case per 10 000 to 15 000 live births. Generally, the diagnosis is made during childhood, although it can be asymptomatic until adulthood, which makes its diagnosis an incidental finding during routine examinations. Few cases have been described. We report the case of a 40-year- old female patient, who was referred to the emergency department of our &#8220;Hospital del Tórax&#8221; for presenting chest pain, dyspnea of medium efforts and fever of one month of evolution.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Anomalías Congénitas]]></kwd>
<kwd lng="es"><![CDATA[Anomalías del Sistema Respiratorio]]></kwd>
<kwd lng="es"><![CDATA[Informes de Casos]]></kwd>
<kwd lng="en"><![CDATA[Congenital Abnormalities]]></kwd>
<kwd lng="en"><![CDATA[Respiratory System Abnormalities]]></kwd>
<kwd lng="en"><![CDATA[Case Reports]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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