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<journal-meta>
<journal-id pub-id-type="pid">S1017-854620040001</journal-id>
<journal-title>Revista Médica del Hospital Nacional de Niños Dr. Carlos Sáenz Herrera</journal-title>
<abbrev-journal-title>Rev. méd. Hosp. Nac. Niños (Costa Rica)</abbrev-journal-title>
<issn>1017-8546</issn>
<publisher>
<publisher-name>Editorial Nacional de Salud y Seguridad Social</publisher-name>
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<article-meta>
<article-id>S1017-85462004000100001</article-id>
<title-group>
<article-title xml:lang="es">Síndrome de activación del macrófago</article-title>
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<given-names>Oscar</given-names>
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<xref ref-type="aff" rid="A01"/>
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<aff id="A01">
<institution>,Caja Costarricense de Seguro Social Hospital Nacional de Niños Dr. Carlos Sáenz Herrera </institution>
<addr-line> </addr-line>
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<pub-date pub-type="pub">
<year>2004</year>
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<pub-date pub-type="epub">
<year>2004</year>
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<volume>39</volume>
<fpage>05</fpage>
<lpage>11</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http:/www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S1017-85462004000100001&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S1017-85462004000100001&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S1017-85462004000100001&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p>El síndrome de activación del macrófago (SAM) en un proceso inflamatorio secundario a una activación del sistema mononuclear fagocítico, con proliferación de histiocitos y hemofagocitosis (HF). Se caracteriza por pancitopenia, insuficiencia hepática, coagulopatía y síntomas neurológicos. Es causado por la activación y proliferación sin control de linfocitos T y de macrófagos, que llevan a una sobreproducción de citoquinas. Se han descrito una forma primaria o familiar y una secundaria asociada a infección y enfermedades reumáticas principalmente (10) La característica más frecuente del síndrome es la presencia en médula ósea o tejidos de hemofagocitosis. Los estudios de laboratorio muestran citopenias, hipertrigliceridemia, aumento en la ferritina y una coagulopatía con hipofibrinogenemia. El tratamiento usual en el cuadro agudo es terapia con pulsos de metilprednisolona</p></abstract>
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<self-uri xlink:href="http:/www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S1017-85462004000100002&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S1017-85462004000100002&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S1017-85462004000100002&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p>La alergia al látex de hule natural, se ha convertido en un problema importante de salud en los trabajadores de la salud y en pacientes con espina bífida e intervenciones quirúrgicas múltiples. El tratamiento curativo con inmunoterapia no produce una solución al problema.Las medidas preventivas permiten reducir la incidencia de la alergia al látex y son una mejor estrategia para intervenir en este problema de salud pública. Con el objetivo de aumentar el conocimiento sobre el problema de alergia al látex, discutimos los aspectos relacionados con historia, epidemiología, diagnóstico, prevención y tratamiento. Se definen los términos sensibilización y alergia y se describen los aspectos químicos del látex de hule natural y de sus proteínas. La definición de grupos de riesgo permite desarrollar una estrategia en las intituciones de salud que disminuye la exposición y como consecuencia las manifestaciones clínicas de los individuos sensibilizados</p></abstract>
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