<?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>2176-6223</journal-id>
<journal-title><![CDATA[Revista Pan-Amazônica de Saúde]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Pan-Amaz Saude]]></abbrev-journal-title>
<issn>2176-6223</issn>
<publisher>
<publisher-name><![CDATA[Instituto Evandro Chagas. Secretaria de Vigilância em Saúde e Ambiente. Ministério da Saúde]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2176-62232016000100003</article-id>
<article-id pub-id-type="doi">10.5123/s2176-62232016000100003</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Linfoma de Hodgkin: aspectos epidemiológicos e subtipos diagnosticados em um hospital de referência no Estado do Pará, Brasil]]></article-title>
<article-title xml:lang="en"><![CDATA[Hodgkin lymphoma: epidemiológica! aspects and subtypes diagnosed in a reference hospital in Pará State, Brazil]]></article-title>
<article-title xml:lang="es"><![CDATA[Linfoma de Hodgkin: aspectos epidemiológicos y subtipos diagnosticados en un hospital de referencia en el Estado de Pará, Brasil]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Monteiro]]></surname>
<given-names><![CDATA[Talita Antonia Furtado]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Arnaud]]></surname>
<given-names><![CDATA[Maria Vanda Catão]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Monteiro]]></surname>
<given-names><![CDATA[José Luiz Furtado]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Costa]]></surname>
<given-names><![CDATA[Marcos Rogério Menezes da]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vasconcelos]]></surname>
<given-names><![CDATA[Pedro Fernando da Costa]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Instituto Evandro Chagas/SVS/MS Seção de Virologia ]]></institution>
<addr-line><![CDATA[Ananindeua Pará]]></addr-line>
<country>Brasil</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital Ophir Loyola Departamento de Patologia ]]></institution>
<addr-line><![CDATA[Belém Pará]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Centro Universitário do Estado do Pará  ]]></institution>
<addr-line><![CDATA[Belém Pará]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Universidade Federal do Pará Núcleo de Medicina Tropical ]]></institution>
<addr-line><![CDATA[Belém Pará]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="Af5">
<institution><![CDATA[,Instituto Evandro Chagas/SVS/MS Seção de Arbovirologia e Febres Hemorrágicas ]]></institution>
<addr-line><![CDATA[Ananindeua Pará]]></addr-line>
<country>Brasil</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2016</year>
</pub-date>
<volume>7</volume>
<numero>1</numero>
<fpage>27</fpage>
<lpage>31</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.iec.gov.br/scielo.php?script=sci_arttext&amp;pid=S2176-62232016000100003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.iec.gov.br/scielo.php?script=sci_abstract&amp;pid=S2176-62232016000100003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.iec.gov.br/scielo.php?script=sci_pdf&amp;pid=S2176-62232016000100003&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[RESUMO Os linfomas são neoplasias do sistema imunitário com origem em linfócitos B, T ou células natural killer que envolvem os tecidos linfoides que estão associados ao crescimento de massas tumorais. O linfoma de Hodgkin (LH) é uma neoplasia linfoproliferativa caracterizada histopatologicamente pela presença de células neoplásicas com variada morfologia denominadas Reed-Sternberg. O objetivo deste trabalho foi descrever o perfil epidemiológico e subtipos dos LH diagnosticados no período de 1996 a 2005 no Hospital Ophir Loyola em Belém, Estado do Pará, Brasil. Do total, 64,6% (42/65) dos pacientes com LH eram do sexo masculino e 35,4% (23/65) do feminino com faixa etária variando entre 2 e 84 anos. Os subtipos de LH registraram taxas de 50,8% (33/65), 26,2% (17/65), 15,4% (10/65) e 7,6% (5/65) para esclerose nodular, celularidade mista, depleção linfocitária e predominância linfocitária, respectivamente. Os LH, na década do estudo (1996-2005), foram mais expressivos na faixa infanto-juvenil, na qual prevaleceu o subtipo esclerose nodular nas amostras diagnosticadas no Estado do Pará.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT Lymphomas are neoplasias of the immune system originating from B and T cells or natural killer cells which involve lymphoid tissues that are associated with the growth of tumor masses. Hodgkin's lymphoma (HL) is a lymphoproliferative malignancy characterized pathologically by the presence of neoplastic cells with a different morphology called Reed-Sternberg. The aim of this study was to describe the epidemiological profile and subtypes of HL diagnosed from 1996 to 2005 at Ophir Loyola Hospital in Belém, Pará State, Brazil. Of the total, 64.6% (42/65) of patients with HL were male and 35.4% (23/65) of women with ages ranging from 2 to 84 years old. HL subtypes reported rates of 50.8% (33/65), 26.2% (17/65), 15.4% (10/65) and 7.6% (5/65) to nodular sclerosis, mixed cellularity, lymphocyte depletion and lymphocyte predominance, respectively. HL, in the period of the current study (1996-2005), it was more expressive in groups of children and teenagers which prevailed the nodular sclerosis subtype in samples diagnosed in the Pará State.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN Los linfomas son neoplasias del sistema inmunitario con origen en linfocitos B, T o células natural killer que envuelven los tejidos linfoides que están asociados al crecimiento de masas tumorales. El linfoma de Hodgkin (LH) es una neoplasia linfoproliferativa caracterizada histopatológicamente por la presencia de células neoplásicas con una morfología variada, denominadas Reed-Sternberg. El objetivo de este trabajo fue el de describir el perfil epidemiológico y los subtipos de los LH diagnosticados en el período de 1996 a 2005 en el Hospital Ophir Loyola en Belém, Estado de Pará, Brasil. Del total, 64,6% (42/65) de los pacientes con LH eran del sexo masculino y 35,4% (23/65) del femenino con una franja etaria variando entre 2 y 84 años. Los subtipos de LH registraron tasas de 50,8% (33/65), 26,2% (17/65), 15,4% (10/65) y 7,6% (5/65) para esclerosis nodular, celularidad mixta, depleción linfocitaria y predominancia linfocitaria, respectivamente. Los LH, en la década del estudio (1996-2005), fueron más expresivos en la franja infanto-juvenil, en la cual prevaleció el subtipo esclerosis nodular en las muestras diagnosticadas en el Estado de Pará.]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[Linfoma de Hodgkin]]></kwd>
<kwd lng="pt"><![CDATA[Perfil de Saúde]]></kwd>
<kwd lng="pt"><![CDATA[Células de Reed-Sternberg]]></kwd>
<kwd lng="en"><![CDATA[Hodgkin Lymphoma]]></kwd>
<kwd lng="en"><![CDATA[Health Profile]]></kwd>
<kwd lng="en"><![CDATA[Reed-Sternberg Cells]]></kwd>
<kwd lng="es"><![CDATA[Linfoma de Hodgkin]]></kwd>
<kwd lng="es"><![CDATA[Perfil de Salud]]></kwd>
<kwd lng="es"><![CDATA[Células de Reed-Sternberg]]></kwd>
</kwd-group>
</article-meta>
</front><back>
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