<?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>S0028-37462022000100061</article-id>
<article-id pub-id-type="doi">10.35366/105534</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síndrome de hiper-IgE y úlcera eosinofílica en mucosa oral]]></article-title>
<article-title xml:lang="en"><![CDATA[Hyper IgE syndrome and eosinophilic ulcer]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vinitzky-Brener]]></surname>
<given-names><![CDATA[Ilan]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Carrasco-Rueda]]></surname>
<given-names><![CDATA[Carlos Alberto]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ángeles-Gálvez]]></surname>
<given-names><![CDATA[Mariana]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Alejandre-García]]></surname>
<given-names><![CDATA[Alejandro]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2022</year>
</pub-date>
<volume>81</volume>
<numero>1</numero>
<fpage>61</fpage>
<lpage>64</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0028-37462022000100061&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0028-37462022000100061&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0028-37462022000100061&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen: El síndrome de hiper-IgE (SHIE) es una inmunodeficiencia primaria y trastorno poco frecuente, se caracteriza por un elevado nivel de IgE sérica, con manifestaciones cutáneas (eccema, abscesos o infecciones) e infecciones pulmonares recurrentes. Dicho trastorno se presenta en dos patrones genéticos: autosómica dominante (AD-SHIE) y autosómica recesiva (AR-SHIE). La úlcera eosinofílica (UE) de la mucosa oral se describe como una lesión benigna, autolimitada con alta predilección por la mucosa ventral de la lengua. Su diagnóstico se establece a partir del estudio histopatológico. Presentamos el caso de paciente masculino de 10 años de edad, diagnosticado con síndrome de hiper-IgE, con presencia de úlcera eosinofílica en la mucosa oral de dos meses de evolución.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract: Hyper-IgE syndrome is a rare disorder characterized by elevated serum IgE, with skin manifestations (abscessed, eczema and infections) and recurrent pulmonary infections. This disorder occurs in two genetic patterns: Autosomal dominant (AD-HIES) and Autosomal recessive (AR-HIES). Eosinophilic ulcer of the oral mucosa is described as a benign, self-limited lesion with high predilection for the ventral mucosa of the tongue. Its diagnosis is established by histopathological study. We report the case of a 10-year-old male patient diagnosed with Hyper IgE Syndrome, with presence of Eosinophilic Ulcer in the oral mucosa, with approximately two months of evolution.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Síndrome hiperinmunoglobulina E]]></kwd>
<kwd lng="es"><![CDATA[úlcera eosinofílica]]></kwd>
<kwd lng="es"><![CDATA[mucosa oral]]></kwd>
<kwd lng="en"><![CDATA[Hyper IgE syndrome]]></kwd>
<kwd lng="en"><![CDATA[eosinophilic ulcer]]></kwd>
<kwd lng="en"><![CDATA[oral mucosa]]></kwd>
</kwd-group>
</article-meta>
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