<?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>0026-1742</journal-id>
<journal-title><![CDATA[Revista de la Facultad de Medicina (México)]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Fac. Med. (Méx.)]]></abbrev-journal-title>
<issn>0026-1742</issn>
<publisher>
<publisher-name><![CDATA[Universidad Nacional Autónoma de México, Facultad de Medicina]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0026-17422018000600026</article-id>
<article-id pub-id-type="doi">10.22201.fm.24484865e.2018.61.6.04</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Oreja de Stahl y su manejo quirúrgico]]></article-title>
<article-title xml:lang="en"><![CDATA[Stahl ear and its surgical management]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Baldín]]></surname>
<given-names><![CDATA[André Víctor]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Telich Tarriba]]></surname>
<given-names><![CDATA[José E]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Íñigo Arroyo]]></surname>
<given-names><![CDATA[Federico]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Apellaniz Campo]]></surname>
<given-names><![CDATA[Armando]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital General Dr. Manuel Gea González  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital General Dr. Manuel Gea González  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2018</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2018</year>
</pub-date>
<volume>61</volume>
<numero>6</numero>
<fpage>26</fpage>
<lpage>28</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0026-17422018000600026&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0026-17422018000600026&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0026-17422018000600026&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN  Introducción: La oreja de Stahl presenta una baja incidencia, aún en centros especializados de reconstrucción auricular. Se caracteriza por presentar un remanente cartilaginoso anormal que se extiende desde el antihélix hasta el borde del hélix, formando una tercer crura.  Caso clínico: Varón de 17 años de edad, con deformidad auricular caracterizada por hipoplasia de la raíz del antihélix y presencia de una tercer crura, que comunica el antihélix al hélix. Se realiza resección de la tercer crura y reconstrucción cartilaginosa del pabellón auricular, logrando una adecuada reconstrucción, con buen resultado estético, sin alteración de tamaño en comparación con la oreja contralateral.  Conclusiones: Esta es una rara deformidad auricular, muchas veces subdiagnosticada, incluso en centros especializados. Puede acarrear trastornos y estigmas sociales importantes al paciente. El tratamiento quirúrgico es manejo preferencial, y se centra principalmente en la corrección de la tercer crura.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Introduction: Stahl's ear presents a low incidence, even in specialized ear reconstruction centers. It is characterized by an abno rmal cartilaginous remnant, extending from the antihelix to the edge of the helix, forming a third crura.  Case report: A 17-year-old man presented an ear deformity characterized by hypoplasia of the root of the antihelix and the presence of a third crura, which communicates the antihelix to the helix. A resection of third crura and cartilaginous reconstruction of the auricular pavilion was performed, achieving an adequate reconstruction, with good aesthetic results, without size alteration in comparison to the contralateral ear.  Conclusions: Stahl's deformity is a rare ear deformity that can lead to significant social disruption and stigma. Surgical treatment is the preferential option for handling this deformity, and focuses mainly on the correction of the third crura.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Oreja]]></kwd>
<kwd lng="es"><![CDATA[Stahl]]></kwd>
<kwd lng="es"><![CDATA[reconstrucción auricular]]></kwd>
<kwd lng="en"><![CDATA[Ear]]></kwd>
<kwd lng="en"><![CDATA[Stahl]]></kwd>
<kwd lng="en"><![CDATA[ear reconstruction]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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