<?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>1025-0255</journal-id>
<journal-title><![CDATA[Revista Archivo Médico de Camagüey]]></journal-title>
<abbrev-journal-title><![CDATA[AMC]]></abbrev-journal-title>
<issn>1025-0255</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Ciencias Médicas de Camagüey]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1025-02552019000500681</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Tumores óseos en edad pediátrica]]></article-title>
<article-title xml:lang="en"><![CDATA[Bone tumor in the pediatric age]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rodríguez-Rodríguez]]></surname>
<given-names><![CDATA[Eugenio Isidro]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Taura-Suárez]]></surname>
<given-names><![CDATA[Leonardo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de Ciencias Médicas de Camagüey Hospital Pediátrico Universitario Eduardo Agramonte Piña Servicio de Ortopedia y Traumatología Pediátrica]]></institution>
<addr-line><![CDATA[Camagüey ]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>10</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>10</month>
<year>2019</year>
</pub-date>
<volume>23</volume>
<numero>5</numero>
<fpage>681</fpage>
<lpage>693</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S1025-02552019000500681&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S1025-02552019000500681&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S1025-02552019000500681&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN  Fundamento:  los tumores óseos algunas veces son difíciles de diagnosticar, estos se dividen en benignos y malignos, los benignos son lo más frecuente y entre de ellos el osteocondroma es el principal. Los malignos a pesar de su baja frecuencia tienen importancia por su alta mortalidad, que varía entre 80 a 95 %, y las graves secuelas físicas y emocionales que acarrea su tratamiento en los pacientes. Los tipos de tumor óseo maligno más frecuente son el sarcoma de Ewing y el sarcoma osteogénico.  Objetivo:  profundizar los conocimientos de los tumores óseos en edad pediátrica.  Métodos:  la búsqueda de la información se realizó en un periodo de cinco meses (primero de agosto de 2017 al 31 de diciembre de 2017) y se emplearon las siguientes palabras claves: bone neoplasms y Childhood, a partir de la información obtenida se realizó una revisión bibliográfica de un total de 246 artículos publicados en las bases de datos PubMed, Hinari, Medline y SciELO y mediante el gestor de búsqueda y administrador de referencias EndNote, de ellos se utilizaron 50 citas seleccionadas para realizar la revisión, 40 de ellas de los últimos cinco años, donde se incluyeron dos libros.  Resultados:  se abordan formas de presentación clínica de los tumores óseos y los estudios de tipo imagenológicos, de laboratorio e histológicos. Se describen modalidades de tratamiento tanto conservador como quirúrgico.  Conclusiones:  los tumores óseos benignos en edad pediátrica son más frecuente y en ellos predomina los osteocondroma y entre los malignos el tumor de Ewing y el sarcoma osteogénico.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Background:  bone tumors are sometimes difficult to diagnose, they are divided into benign and malignant, benign tumors are the most frequent and among them the Osteochondroma is the main one. The malignant ones in spite of their low frequency are important for their high mortality, which varies between 80 to 95%, and the serious physical and emotional consequences that their treatment brings to patients. The most common malignant bone tumor types are Ewing's sarcoma and osteogenic sarcoma.  Objective:  to deepen the knowledge of bone tumors in pediatric age.  Methods:  the search of the information was made in a period of five months (from August 1st, 2017 to December 31st, 2017) and the following key words were used: bone neoplasms and Childhood, from the information obtained a bibliographical review of a total of 246 articles published in PubMed, Hinari, Medline, and SciELO databases was made through the EndNote search manager and reference manager, of which 50 selected citations were used to perform the review, 40 of them from the last five years, where two books were included.  Results:  forms of clinical presentation of bone tumors and imaging, laboratory and histological studies are addressed. Both conservative and surgical treatment modalities are described.  Conclusions:  benign osseous tumors in the pediatric age are more frequent and osteochondroma predominates in them and malignant tumors include Ewing tumor and osteogenic sarcoma.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[NEOPLASIAS ÓSEAS/diagnóstico por imagen]]></kwd>
<kwd lng="es"><![CDATA[OSTEOCONDROMA/diagnóstico por imagen]]></kwd>
<kwd lng="es"><![CDATA[OSTEOSARCOMA/diagnóstico por imagen]]></kwd>
<kwd lng="es"><![CDATA[SARCOMA DE EWING/diagnóstico por imagen]]></kwd>
<kwd lng="es"><![CDATA[NIÑO]]></kwd>
<kwd lng="en"><![CDATA[BONE NEOPLASMS/diagnostic imaging]]></kwd>
<kwd lng="en"><![CDATA[OSTEOCHONDROMA/diagnostic imaging]]></kwd>
<kwd lng="en"><![CDATA[OSTEOSARCOMA/diagnostic imaging]]></kwd>
<kwd lng="en"><![CDATA[SARCOMA, EWING/diagnostic imaging]]></kwd>
<kwd lng="en"><![CDATA[CHILD]]></kwd>
</kwd-group>
</article-meta>
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