<?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>S0026-17422019000200043</article-id>
<article-id pub-id-type="doi">10.22201/fm.24484865e.2019.62.2.08</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Tumor de Askin]]></article-title>
<article-title xml:lang="en"><![CDATA[Askin&#8217;s tumor]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Argüello Ramírez]]></surname>
<given-names><![CDATA[Verónica]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rico Nava]]></surname>
<given-names><![CDATA[Araceli]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gutiérrez Ruiz]]></surname>
<given-names><![CDATA[Francisco]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Martínez Renteria]]></surname>
<given-names><![CDATA[Dalia Araceli]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pliego Maldonado]]></surname>
<given-names><![CDATA[Roberto]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Espinosa Soberanes]]></surname>
<given-names><![CDATA[Juan Armando]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Nacional Autónoma de México Facultad de Medicina ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital Central Norte Pemex  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Hospital Central Norte Pemex  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Hospital Central Norte Pemex  ]]></institution>
<addr-line><![CDATA[Ciudad de México ]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>04</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>04</month>
<year>2019</year>
</pub-date>
<volume>62</volume>
<numero>2</numero>
<fpage>43</fpage>
<lpage>47</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0026-17422019000200043&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0026-17422019000200043&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0026-17422019000200043&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen El tumor de Askin es una rara neoplasia de la pared torácica que pertenece al grupo de tumores neuroectodérmicos primitivos que incluyen desde el sarcoma de Ewing hasta el neuroepitelioma. Su principal característica es el dolor. Los tumores neuroectodérmicos primitivos (PNET) derivan de células pluripotenciales neuroectodérmicas de la cresta neural y pertenecen al grupo de tumores de células pequeñas redondas y azules que se caracterizan por un comportamiento agresivo, con manifestaciones clínicas diversas que dependen de su localización anatómica. La localización más común es la toracopulmonar, seguida por el área pélvica. Las metástasis normalmente afectan a los pulmones, huesos, hígado y cerebro. Su diagnóstico se basa en estudios imagenológicos y se confirma con el estudio de histopatología en biopsia o en la resección quirúrgica.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract The Askin&#8217;s tumor is a rare neoplasm of the chest wall that belongs to the group of primitive neuroectodermal tumors (PNETs), which are derivatives from neuroectodermal pluripotent neural crest cells. The range of this type of tumors covers from Ewing&#8217;s sarcoma to the neuroepithelioma and they belong to the group of small round blue cells tumors which are characterized for having an aggressive behavior with diverse clinical manifestations depending on their anatomical location. The most common location for the Askin&#8217;s tumor is the thoracopulmonary area followed by the pelvic area and in the case of metastases the lungs, bones, liver and brain are the most affected parts. In order to identify this disease, the diagnosis of this type of tumor consists on image studies and the confirmation is made through a hispathology biopsy or surgical resection.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Tumor de Askin]]></kwd>
<kwd lng="es"><![CDATA[enolasa]]></kwd>
<kwd lng="es"><![CDATA[tumores neuroectodérmicos]]></kwd>
<kwd lng="en"><![CDATA[Askin&#8217;s tumor]]></kwd>
<kwd lng="en"><![CDATA[enolasa]]></kwd>
<kwd lng="en"><![CDATA[neurodermal tumors (PNETs)]]></kwd>
</kwd-group>
</article-meta>
</front><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Llombart-Bosch]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Contesso]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Peydro-Olaya]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Histology, immunohistochemistry and electron microscopy of small round cell tumors of bone]]></article-title>
<source><![CDATA[Semin Diagn Pathol]]></source>
<year>1996</year>
<volume>13</volume>
<page-range>153-70</page-range></nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Suarez May]]></surname>
<given-names><![CDATA[MA]]></given-names>
</name>
<name>
<surname><![CDATA[Osorio Valero]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Tumor de Askin: Presentación de un caso clínico y revisión de literatura]]></article-title>
<source><![CDATA[Anales de Radiología]]></source>
<year>2008</year>
<volume>1</volume>
<page-range>55-60</page-range><publisher-loc><![CDATA[México ]]></publisher-loc>
</nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Potratz]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Dirksen]]></surname>
<given-names><![CDATA[U]]></given-names>
</name>
<name>
<surname><![CDATA[Jurgens]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Craft]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Ewing Sarcoma: Clinical State-of-the-Art]]></article-title>
<source><![CDATA[Pediatr Hematol Oncol]]></source>
<year>2012</year>
<volume>29</volume>
<page-range>111</page-range></nlm-citation>
</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bravo-Linares]]></surname>
<given-names><![CDATA[David]]></given-names>
</name>
<name>
<surname><![CDATA[Hernández-Verbel]]></surname>
<given-names><![CDATA[Katherine]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Tumor neuroectodérmico primitivo de la pared torácica: tumor de Askin en niño]]></article-title>
<source><![CDATA[Rev. Fac. Med]]></source>
<year>2013</year>
<volume>61</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>239-46</page-range></nlm-citation>
</ref>
<ref id="B5">
<label>5</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Davidoff]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Fernandez]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
<name>
<surname><![CDATA[Santana]]></surname>
<given-names><![CDATA[V]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[The role of neoadjuvant chemotherapy in children with malignant solid tumors]]></article-title>
<source><![CDATA[Semin Pediatr Surg]]></source>
<year>2012</year>
<volume>21</volume>
<page-range>88-99</page-range></nlm-citation>
</ref>
<ref id="B6">
<label>6</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Indelicato]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Keole]]></surname>
<given-names><![CDATA[SR]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Chest wall ewing sarcoma family of tumors: long-term outcomes]]></article-title>
<source><![CDATA[Int. J. Radiation Oncology Biol Phys]]></source>
<year>2011</year>
<volume>81</volume>
<page-range>158-66</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
