<?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>1996-3696</journal-id>
<journal-title><![CDATA[Revista del Instituto de Medicina Tropical]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Inst. Med. Trop.]]></abbrev-journal-title>
<issn>1996-3696</issn>
<publisher>
<publisher-name><![CDATA[Instituto de Medicina Tropical]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1996-36962018000200031</article-id>
<article-id pub-id-type="doi">10.18004/imt/201813231-38</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[PIODERMA GANGRENOSO EN PEDIATRÍA. A PROPÓSITO DE UN CASO]]></article-title>
<article-title xml:lang="en"><![CDATA[PYODERMA GANGRENOSUM IN PEDIATRICS. ABOUT A CASE]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Zárate]]></surname>
<given-names><![CDATA[Claudia]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Salas]]></surname>
<given-names><![CDATA[Iván]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cáceres]]></surname>
<given-names><![CDATA[Andrea]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Apodaca]]></surname>
<given-names><![CDATA[Silvio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Araya]]></surname>
<given-names><![CDATA[Soraya]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lovera]]></surname>
<given-names><![CDATA[Dolores]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Arbo]]></surname>
<given-names><![CDATA[Antonio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Instituto de Medicina Tropical Servicio de Pediatría ]]></institution>
<addr-line><![CDATA[Asunción ]]></addr-line>
<country>Paraguay</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>13</volume>
<numero>2</numero>
<fpage>31</fpage>
<lpage>38</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.iics.una.py/scielo.php?script=sci_arttext&amp;pid=S1996-36962018000200031&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.iics.una.py/scielo.php?script=sci_abstract&amp;pid=S1996-36962018000200031&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.iics.una.py/scielo.php?script=sci_pdf&amp;pid=S1996-36962018000200031&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN El pioderma gangrenoso (PG) es una ulceración cutánea poco común, generalmente idiopática, asociada o no a trastornos sistémicos. La etiopatogenia del PG aún no se conoce bien. Clínicamente se clasifica en tipos ulcerativo, pustular, bulloso y vegetativo. También se han descrito algunas variantes atípicas y raras. El diagnóstico clínico, apoyado en estudios auxiliares (laboratoriales, anatomopatológicos). Se han propuesto algunos criterios para el diagnóstico de PG. El tratamiento consiste principalmente en corticosteroides y agentes inmunosupresores. Caso clínico: adolescente, femenino, sin patología de base, con antecedente de lesión ulcerosa en pierna derecha de 6 meses de evolución, que aumenta de tamaño en el tiempo, consulta en varias oportunidades con tratamientos ambulatorios tórpidos. Ante aparición de fiebre, dolor e impotencia funcional se interna. En el transcurso de la internación presenta rectorragia importante con descenso de Hb. Se realiza colonoscopia de urgencias y se logra unidad diagnóstica egresando con tratamiento apropiado luego de 26 DDI.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT Pyoderma gangrenosum (PG) is an uncommon cutaneous ulceration, usually idiopathic, associated or not with systemic disorders. The etiopathogenesis of PG is still not well understood. Clinically, it is classified into ulcerative, pustular, bullous and vegetative types. Some atypical and rare variants have also been described. The clinical diagnosis, supported by auxiliary studies (laboratorial, anatomopathological). Some criteria have been proposed for the diagnosis of PG. The treatment consists mainly of corticosteroids and immunosuppressive agents. Clinical case: adolescent, female, without basic pathology, with a history of ulcerative lesion in the right leg of 6 months of evolution, which increases in size over time, consulting on several occasions with torpid ambulatory treatments. In the presence of fever, pain and functional impotence is internal. In the course of hospitalization, it presents significant rectorrhagia with a decrease in Hb. An emergency colonoscopy is performed and a diagnostic unit is achieved with appropriate treatment after 26 DDI.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Pioderma gangrenoso]]></kwd>
<kwd lng="es"><![CDATA[enfermedad de chron]]></kwd>
<kwd lng="es"><![CDATA[pediatría]]></kwd>
<kwd lng="en"><![CDATA[Pyoderma gangrenosum]]></kwd>
<kwd lng="en"><![CDATA[Crohn's disease]]></kwd>
<kwd lng="en"><![CDATA[pediatrics]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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