<?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>1405-0099</journal-id>
<journal-title><![CDATA[Cirujano general]]></journal-title>
<abbrev-journal-title><![CDATA[Cir. gen]]></abbrev-journal-title>
<issn>1405-0099</issn>
<publisher>
<publisher-name><![CDATA[Asociación Mexicana de Cirugía General A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1405-00992017000100037</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síndrome de McCune-Albright en un adolescente. Informe de un paciente]]></article-title>
<article-title xml:lang="en"><![CDATA[McCune-Albright syndrome in an adolescent youngster]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Uribe González]]></surname>
<given-names><![CDATA[Guillermo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sigler Morales]]></surname>
<given-names><![CDATA[Luis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Asociación Mexicana de Cirugía General  ]]></institution>
<addr-line><![CDATA[Tijuana BC]]></addr-line>
<country>México</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,aff2  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2017</year>
</pub-date>
<volume>39</volume>
<numero>1</numero>
<fpage>37</fpage>
<lpage>40</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1405-00992017000100037&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1405-00992017000100037&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1405-00992017000100037&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen:  Introducción: Éste es un síndrome muy raro, no hereditario, aparente desde el nacimiento o juventud, identificado clínicamente por displasia ósea, manchas en la piel y pubertad precoz; es originado por alteración del cromosoma 20. El objetivo de este trabajo es presentar el caso de un adolescente que acudió a consulta por una úlcera en la planta de un pie; tenía, además, manifestaciones de este síndrome.  Caso clínico:  Joven de 16 años que radicaba en una población rural alejada; acudió a consulta por presentar una úlcera en la planta del pie derecho, de varios meses de evolución. Tenía acortamiento de la extremidad inferior derecha, manchas de color café con leche en diversas partes del cuerpo, evidencia de desarrollo anormal de las extremidades y una zona de alopecia areata en la cabeza. Se le dieron indicaciones respecto a la úlcera del pie con el uso de aseo, vendas, plantilla para elevar el pie, y se le ofreció una cita para indicar otros estudios y referencia a otros especialistas, pero no regresó. Posteriormente, con su familia, cambió de domicilio. Los hallazgos a la exploración permitieron establecer el diagnóstico clínico de síndrome de McCune-Albright.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract:  Introduction:  This is a non-hereditary, very rare syndrome, present since birth or youth; it is due to an alteration in the chromosome 20. The objective of this work is to present the case of a male adolescent who consulted because of an ulcer in the sole of the right foot; he also showed signs of this syndrome.  Case report: 16-year-old male who lived in a distant rural zone; he complained of an ulcer in the sole of the right foot for several months. There was shortness of the right lower extremity, cafe-au-lait pigmented skin lesions, abnormal development of limbs and alopecia areata of the scalp. Cleaning of the ulcer, bandages, sole protector, and rest were recommended. A future work-up with X rays and consultations was planned, but he never came back. Later, he changed his address. Clinical findings were the basis of the diagnosis of McCune-Albright syndrome.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Síndrome de McCune-Albright]]></kwd>
<kwd lng="es"><![CDATA[adolescente varón]]></kwd>
<kwd lng="es"><![CDATA[alopecia areata]]></kwd>
<kwd lng="en"><![CDATA[McCune-Albright syndrome]]></kwd>
<kwd lng="en"><![CDATA[adolescent male]]></kwd>
<kwd lng="en"><![CDATA[alopecia areata]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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