<?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>0101-5907</journal-id>
<journal-title><![CDATA[Revista Paraense de Medicina]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Para. Med.]]></abbrev-journal-title>
<issn>0101-5907</issn>
<publisher>
<publisher-name><![CDATA[Fundação Santa Casa de Misericórdia do Pará]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0101-59072006000400006</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Relação dos níveis séricos do CEA com o acometimento linfonodal regional no pré-operatório do câncer gástrico]]></article-title>
<article-title xml:lang="en"><![CDATA[Relation of serum levels of CEA whit the attack regional lymph in preoperative patients with gastric cancer]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pacheco]]></surname>
<given-names><![CDATA[Antônio Carlos Chalu]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lima]]></surname>
<given-names><![CDATA[Isamu Komatsu]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Conceição Júnior]]></surname>
<given-names><![CDATA[Vítor Moutinho da]]></given-names>
</name>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Mestre em Gastroenterologia cirúrgica pela UNIFESP-EPM/SP  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A02">
<institution><![CDATA[,Residente de Cancerologia cirúrgica do Hospital Ophir Loyola  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A03">
<institution><![CDATA[,Residente de Cirurgia geral do Hospital Ophir Loyola  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2006</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2006</year>
</pub-date>
<volume>20</volume>
<numero>4</numero>
<fpage>29</fpage>
<lpage>33</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.iec.gov.br/scielo.php?script=sci_arttext&amp;pid=S0101-59072006000400006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.iec.gov.br/scielo.php?script=sci_abstract&amp;pid=S0101-59072006000400006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.iec.gov.br/scielo.php?script=sci_pdf&amp;pid=S0101-59072006000400006&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Objetivo: analisar a relação entre os níveis séricos do antígeno carcino-embrionário CEA e o acometimento linfonodal regional no pré-operatório do câncer gástrico. Método: realizado estudo transversal de prevalência de 30 (trinta) doentes com diagnóstico histopatológico de adenocarcinoma gástrico, nos quais o estadiamento clínico não evidenciou doença disseminada ou irressecável. Com esses dados procedeu-se a coleta de amostras de sangue para dosagem do CEA; a seguir, os pacientes foram submetidos à laparotomia com estadiamento intra-operatório. Caso não houvesse sinais de irressecabilidade ou metástase, procedia-se à ressecção radical pretensamente curativa que consistia de gastrectomia subtotal ou total, omentectomia maior e menor e linfadenectomia a D2. Procedeu-se o exame microscópico de todos os linfonodos ressecados os quais foram, previamente, corados com hematoxilina-eosina. Resultado: CEA alterado no pré-operatório em 06 (seis) pacientes (20%). Observou-se metástase, em um ou mais linfonodos em 17 doentes (56,66%). Conclusão: não houve correlação significante entre níveis séricos pré-operatórios do CEA com acometimento linfonodal regional em pacientes com câncer gástrico submetidos à ressecção gástrica com intenção curativa (p>0,05).]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Objective: study a possible relation between serum levels of CEA and the lymph-node acess of the patient who have gastric adenocarcinoma. Method: transversalis analysis of 30 (thirty) patients carriers of gastric adenocarcinoma whose clinical and surgical stages have not showed disseminated or non-ressectable disease. With this data, blood samples were collected in order to perform the tumor markers dosage previously mentioned. Then, they were submitted to laparotomy with intraoperatory staging. Whether there were no sings of irressecability or metastases, a pretentiously curative gastrectomy, which could be total or subtotal, with major and minor omentectomy and D2 lyphadenectomy was performed. All lymph-nodes ressected from patients were submitted to hystopathological exam with hematoxilin-eosin preparation. Results and conclusions: CEA levels were above normal in six patients (20%). However, there were metastases in on or more lymph-nodes resected from seventeen patients (56,66%). In order to perform a statistical study of a possible relation between these markers serum levels and lymph-node metastases, Binominal, Kolmogorov-Smirnov and Fisher tests were used, according to the studied variables. Finally, there was no significant correlation between pre-operatory serum levels of the studied markers and regional lymphnodal metastases in gastric cancer patients submitted to gastric ressection with curative intention (p>0,05).]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[antígeno carcino-embrionário]]></kwd>
<kwd lng="pt"><![CDATA[CEA]]></kwd>
<kwd lng="pt"><![CDATA[marcadores tumorais]]></kwd>
<kwd lng="pt"><![CDATA[câncer gástrico]]></kwd>
<kwd lng="pt"><![CDATA[gastrectomia radical]]></kwd>
<kwd lng="en"><![CDATA[carcino-embrionic antigen]]></kwd>
<kwd lng="en"><![CDATA[radical gastrectomy]]></kwd>
<kwd lng="en"><![CDATA[tumor markers]]></kwd>
<kwd lng="en"><![CDATA[gastric cancer]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="right"><font size="2" face="Verdana"><b><a name="topo"></a>ARTIGO ORIGINAL</b></font></p>     <p>&nbsp;</p>     <p><font size="4" face="Verdana"><b>Rela&ccedil;&atilde;o dos n&iacute;veis s&eacute;ricos    do CEA com o acometimento linfonodal regional no pr&eacute;-operat&oacute;rio    do c&acirc;ncer g&aacute;strico<sup><a href="#nota"><font size="3">1</font></a></sup></b></font></p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><b>Relation of serum levels of CEA whit the attack    regional lymph in preoperative patients with gastric cancer.</b></font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font size="2" face="Verdana"><b>Ant&ocirc;nio Carlos Chalu Pacheco<sup>I</sup>;    Isamu Komatsu Lima<sup>II</sup>; V&iacute;tor Moutinho da Concei&ccedil;&atilde;o    J&uacute;nior<sup>III</sup></b></font></p>     <p><font size="2" face="Verdana"> <sup>I</sup>Mestre em Gastroenterologia cir&uacute;rgica    pela UNIFESP-EPM/SP    <br>   <sup>II</sup>Residente de Cancerologia cir&uacute;rgica do Hospital Ophir Loyola    ]]></body>
<body><![CDATA[<br>   <sup>III</sup>Residente de Cirurgia geral do Hospital Ophir Loyola</font></p>     <p><font size="2" face="Verdana"><a href="#endereco">Endere&ccedil;o para correspond&ecirc;ncia</a></font></p>     <p>&nbsp;</p>     <p>&nbsp;</p> <hr size="1" noshade>     <p><font size="2" face="Verdana"><b>RESUMO</b></font></p>     <p><font size="2" face="Verdana"><b><i>OBJETIVO:</i></b><i> analisar a rela&ccedil;&atilde;o    entre os n&iacute;veis s&eacute;ricos do ant&iacute;geno carcino-embrion&aacute;rio    CEA e o acometimento linfonodal regional no pr&eacute;-operat&oacute;rio do    c&acirc;ncer g&aacute;strico.    <br>   <b>M&Eacute;TODO:</b> realizado estudo transversal de preval&ecirc;ncia de 30    (trinta) doentes com diagn&oacute;stico histopatol&oacute;gico de adenocarcinoma    g&aacute;strico, nos quais o estadiamento cl&iacute;nico n&atilde;o evidenciou    doen&ccedil;a disseminada ou irressec&aacute;vel. Com esses dados procedeu-se    a coleta de amostras de sangue para dosagem do CEA; a seguir, os pacientes foram    submetidos &agrave; laparotomia com estadiamento intra-operat&oacute;rio. Caso    n&atilde;o houvesse sinais de irressecabilidade ou met&aacute;stase, procedia-se    &agrave; ressec&ccedil;&atilde;o radical pretensamente curativa que consistia    de gastrectomia subtotal ou total, omentectomia maior e menor e linfadenectomia    a D2. Procedeu-se o exame microsc&oacute;pico de todos os linfonodos ressecados    os quais foram, previamente, corados com hematoxilina-eosina.    <br>   <b>RESULTADO:</b> CEA alterado no pr&eacute;-operat&oacute;rio em 06 (seis)    pacientes (20%). Observou-se met&aacute;stase, em um ou mais linfonodos em 17    doentes (56,66%).    <br>   <b>CONCLUS&Atilde;O:</b> n&atilde;o houve correla&ccedil;&atilde;o significante    entre n&iacute;veis s&eacute;ricos pr&eacute;-operat&oacute;rios do CEA com    acometimento linfonodal regional em pacientes com c&acirc;ncer g&aacute;strico    submetidos &agrave; ressec&ccedil;&atilde;o g&aacute;strica com inten&ccedil;&atilde;o    curativa (p&gt;0,05).</i></font></p>     <p><font size="2" face="Verdana"><b>Descritores:</b> ant&iacute;geno carcino-embrion&aacute;rio,    CEA; marcadores tumorais; c&acirc;ncer g&aacute;strico; gastrectomia radical.</font></p> <hr size="1" noshade>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana"><b>SUMMARY</b></font></p>     <p><font size="2" face="Verdana"> <b>OBJECTIVE:</b> study a possible relation    between serum levels of CEA and the lymph-node acess of the patient who have    gastric adenocarcinoma.    <br>   <b> METHOD:</b> transversalis analysis of 30 (thirty) patients carriers of gastric    adenocarcinoma whose clinical and surgical stages have not showed disseminated    or non-ressectable disease. With this data, blood samples were collected in    order to perform the tumor markers dosage previously mentioned. Then, they were    submitted to laparotomy with intraoperatory staging. Whether there were no sings    of irressecability or metastases, a pretentiously curative gastrectomy, which    could be total or subtotal, with major and minor omentectomy and D2 lyphadenectomy    was performed. All lymph-nodes ressected from patients were submitted to hystopathological    exam with hematoxilin-eosin preparation.    <br>   <b>RESULTS AND CONCLUSIONS: </b>CEA levels were above normal in six patients    (20%). However, there were metastases in on or more lymph-nodes resected from    seventeen patients (56,66%). In order to perform a statistical study of a possible    relation between these markers serum levels and lymph-node metastases, Binominal,    Kolmogorov-Smirnov and Fisher tests were used, according to the studied variables.    Finally, there was no significant correlation between pre-operatory serum levels    of the studied markers and regional lymphnodal metastases in gastric cancer    patients submitted to gastric ressection with curative intention (p&gt;0,05).</font></p>     <p><font size="2" face="Verdana"><b>KEY-WORDS:</b> carcino-embrionic antigen,    radical gastrectomy, tumor markers, gastric cancer.</font></p> <hr size="1" noshade>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><b>INTRODU&Ccedil;&Atilde;O</b></font></p>     <p><font size="2" face="Verdana">O ant&iacute;geno carcino-embrion&aacute;rio    CEA &eacute; uma glicoprote&iacute;na de peso molecular de 200.000 daltons,    encontrada, normalmente, no tubo digestivo fetal, mas inicialmente identificada    em c&eacute;lulas tumorais de c&oacute;lon de um paciente adulto. Com amplia&ccedil;&atilde;o    da casu&iacute;stica, sabese, hoje, que o CEA pode estar alterado em pacientes    com diversos tipos de c&acirc;ncer, pois al&eacute;m do colorretal, os tumores    do pulm&atilde;o, mama, f&iacute;gado e est&ocirc;mago podem provocar eleva&ccedil;&atilde;o    dos n&iacute;veis s&eacute;ricos deste marcador<sup>1</sup>.</font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana">Desde a detec&ccedil;&atilde;o do CEA por GOLD    &amp; FREEDMAN, 1965, ficou provado ser este um marcador &uacute;til para tumores    malignos gastrintestinais<sup>2</sup>. No caso do c&acirc;ncer g&aacute;strico, aferi&ccedil;&otilde;es    pr&eacute;-operat&oacute;rias e p&oacute;soperat&oacute;rias seriadas dos n&iacute;veis    do CEA s&eacute;rico s&atilde;o &uacute;teis em prever o est&aacute;gio do c&acirc;ncer,    progress&atilde;o e recorr&ecirc;ncia<sup>3</sup>.</font></p>     <p><font size="2" face="Verdana">Os marcadores tumorais s&atilde;o subst&acirc;ncias    biol&oacute;gicas, pertencentes aos mais diversos grupos bioqu&iacute;micos,    produzidos pelo tumor ou liberadas pelo hospedeiro, que podem ser quantificadas    por meio de an&aacute;lise de material org&acirc;nico, tal como plasma, ascite,    suco g&aacute;strico e lavado peritoneal. Alguns tumores s&atilde;o produtores    eficientes de marcadores, enquanto outros n&atilde;o <sup>4</sup>.</font></p>     <p><font size="2" face="Verdana">Sua detec&ccedil;&atilde;o apenas na presen&ccedil;a    de c&acirc;ncer, permitiria correlacionar com o volume tumoral, taxa de crescimento    do tumor, estimar presen&ccedil;a de met&aacute;stases, e a resposta ao tratamento    preconizado, por&eacute;m, infelizmente, a maioria dessas subst&acirc;ncias    n&atilde;o &eacute; espec&iacute;fica e tampouco suficientemente sens&iacute;vel    para tais prop&oacute;sitos<sup>4</sup>. Embora se continue buscando marcadores    &uacute;teis para diagn&oacute;stico das neoplasias, este, ainda, &eacute; objetivo    a ser alcan&ccedil;ado. Sua maior aplica&ccedil;&atilde;o at&eacute; o presente,    ainda se restringe ao acompanhamento de pacientes com c&acirc;ncer, como instrumento    de monitora&ccedil;&atilde;o da efic&aacute;cia terap&ecirc;utica e/ou da recidiva    de doen&ccedil;a<sup>1</sup>.</font></p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><b>OBJETIVO</b></font></p>     <p><font size="2" face="Verdana">Analisar a rela&ccedil;&atilde;o entre os n&iacute;veis    s&eacute;ricos pr&eacute;operat&oacute;rios do CEA com o acometimento linfonodal    regional do c&acirc;ncer g&aacute;strico.</font></p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><b>M&Eacute;TODO</b></font></p>     <p><font size="2" face="Verdana"><b>Casu&iacute;stica</b></font></p>     <p><font size="2" face="Verdana">Estudo transversal de preval&ecirc;ncia em 30    pacientes, procedentes do Estado do Par&aacute;, de ambos os sexos, internados    no Hospital Ophir Loyola (HOL), em Bel&eacute;m-Par&aacute;, com diagn&oacute;stico    de c&acirc;ncer g&aacute;strico e submetidos, ap&oacute;s estadiamento, &agrave;    gastrectomia radical D2 em 1999.</font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana">Exclu&iacute;dos os pacientes fumantes, portadores    de afec&ccedil;&otilde;es benignas inflamat&oacute;rias intestinais e pancre&aacute;ticas,    cirrose hep&aacute;tica e de neoplasias de outros &oacute;rg&atilde;os.</font></p>     <p><font size="2" face="Verdana"><b>Procedimento</b></font></p>     <p><font size="2" face="Verdana">Submetidos os pacientes &agrave; coleta de sangue    para dosagem do CEA, em per&iacute;odo compreendido entre 24 e 48 horas antes    do ato operat&oacute;rio.</font></p>     <p><font size="2" face="Verdana">Para determina&ccedil;&atilde;o quantitativa    do CEA empregou - se <i>kit</i> de imunoensaio enzim&aacute;tico de micropart&iacute;culas    por imunofluorometria em aparelho IMX<sup>&reg;</sup> da Abbott. As dosagens    foram realizadas no Departamento de An&aacute;lises Cl&iacute;nicas do HOL.</font></p>     <p><font size="2" face="Verdana">A fluoresc&ecirc;ncia de cada amostra &eacute;    proporcional &agrave; concentra&ccedil;&atilde;o de CEA nela contida, sendo    estabelecido como valor de refer&ecirc;ncia para n&atilde;o fumantes aquele    inferior a 6,5 ng/ml, de acordo com os valores de refer&ecirc;ncia do kit empregado.</font></p>     <p><font size="2" face="Verdana">Durante a gastrectomia radical com dissec&ccedil;&atilde;o    linfonodal a D2, os linfonodos foram dissecados, separadamente, conforme identifica&ccedil;&atilde;o    do cirurgi&atilde;o, por topografia tumoral preconizada pela Classifica&ccedil;&atilde;o    Japonesa de C&acirc;ncer G&aacute;strico (1998).</font></p>     <p><font size="2" face="Verdana">O est&ocirc;mago ressecado, em conjunto com o    grande e pequeno omentos, foi aberto ao longo da grande curvatura expondo-se    toda sua mucosa para aferi&ccedil;&atilde;o e an&aacute;lise das margens cir&uacute;rgicas,    bem como, avalia&ccedil;&atilde;o macrosc&oacute;pica da les&atilde;o.</font></p>     <p><font size="2" face="Verdana">Catalogados os resultados obtidos a partir de    an&aacute;lise dos n&iacute;veis s&eacute;ricos pr&eacute;-operat&oacute;rios    de CEA, do acometimento num&eacute;rico linfonodal, em fichas de avalia&ccedil;&atilde;o    sorol&oacute;gica, macrosc&oacute;pica e histol&oacute;gica. Antes de estudar    a correla&ccedil;&atilde;o entre as vari&aacute;veis da pesquisa e a presen&ccedil;a    de altera&ccedil;&atilde;o dos n&iacute;veis s&eacute;ricos do CEA, foi realizada    an&aacute;lise estat&iacute;stica entre os pacientes que apresentavam n&iacute;veis    do CEA normais e alterados, a fim de realizar o cruzamento entre valores normais    e alterados, em cada vari&aacute;vel do estudo.</font></p>     <p><font size="2" face="Verdana">Comparadas as informa&ccedil;&otilde;es fornecidas    pela an&aacute;lise dos n&iacute;veis s&eacute;ricos pr&eacute;-operat&oacute;rios    do CEA com dados sobre o acometimento linfonodal de cada paciente.</font></p>     <p><font size="2" face="Verdana">Utilizado para an&aacute;lise estat&iacute;stica    o programa Bioestat<sup>&reg;</sup> vers&atilde;o 2-0, compreendendo o Teste    de Kolmogorov-Smirnov, de acordo com a natureza das vari&aacute;veis.</font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana">Estudo aprovado pelo Conselho de &Eacute;tica    deste Hospital e respeitando as normas vigentes do Minist&eacute;rio da Sa&uacute;de.</font></p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><b>RESULTADOS</b></font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p align="center"><img src="/img/revistas/rpm/v20n4/4a06t1.gif" border="0"></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p align="center"><img src="/img/revistas/rpm/v20n4/4a06f1.gif" border="0"></p>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p>&nbsp;</p>     <p align="center"><img src="/img/revistas/rpm/v20n4/4a06t2.gif" border="0"></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p align="center"><img src="/img/revistas/rpm/v20n4/4a06f2.gif" border="0"></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><b>DISCUSS&Atilde;O</b></font></p>     <p><font size="2" face="Verdana">A preval&ecirc;ncia do adenocarcinoma g&aacute;strico    no Estado do Par&aacute; &eacute; elevada e, particularmente, na cidade de Bel&eacute;m,    onde, em rela&ccedil;&atilde;o &agrave; taxa global mundial de incid&ecirc;ncia    ocupa o 19<sup>o</sup> lugar no sexo feminino e o 12<sup>o</sup> lugar no sexo masculino<sup>5</sup>.</font></p>     <p><font size="2" face="Verdana">A utilidade dos marcadores tumorais tem sido    avaliada em uma grande variedade de estudos para an&aacute;lise cl&iacute;nica    multivariada, abordando: est&aacute;gio, resposta &agrave; terapia neoadjuvante,    progress&atilde;o e recorr&ecirc;ncia do c&acirc;ncer<sup>6</sup>. Estes marcadores t&ecirc;m    sido estudados, especialmente, com objetivo de identificar os pacientes com    risco maior de recorr&ecirc;ncia, independentemente do car&aacute;ter curativo    aplicado e, portanto, candidatos &agrave; terapia adjuvante<sup>7</sup>.</font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana">Embora os marcadores tumorais sejam &uacute;teis    no acompanhamento do c&acirc;ncer g&aacute;strico com o intuito de identificar    a recorr&ecirc;ncia tumoral, n&atilde;o est&aacute; claro, atualmente, que papel    essas subst&acirc;ncias representam no pr&eacute;operat&oacute;rio, progn&oacute;stico    e, principalmente, no acometimento linfonodal de pacientes que ser&atilde;o    submetidos &agrave; ressec&ccedil;&atilde;o com inten&ccedil;&atilde;o curativa<sup>8</sup>.</font></p>     <p><font size="2" face="Verdana">Em virtude disso e associado ao fato de serem    escassos os trabalhos que correlacionam os n&iacute;veis s&eacute;ricos pr&eacute;-operat&oacute;rios    dos marcadores tumorais - CEA e o acometimento dos linfonodos regionais, foram    avaliados pacientes em uma &aacute;rea de alta incid&ecirc;ncia da neoplasia.</font></p>     <p><font size="2" face="Verdana">Al&eacute;m disso, a escassa literatura que estuda    o papel dos marcadores tumorais no progn&oacute;stico pr&eacute;-operat&oacute;rio,    no que tange ao acometimento dos linfonodos regionais, &eacute; conflitante    com a extensa fonte bibliogr&aacute;fica que estuda seu valor no acompanhamento    p&oacute;s-operat&oacute;rio.</font></p>     <p><font size="2" face="Verdana">Em rela&ccedil;&atilde;o ao CEA, foram inclu&iacute;dos    apenas os pacientes com n&iacute;veis elevados do mesmo, adotando como valores    de refer&ecirc;ncia, resultados superiores a 6,5 ng/ml, de acordo com o kit    utilizado no estudo. &Eacute; sabido que o fumo, algumas afec&ccedil;&otilde;es    benignas inflamat&oacute;rias intestinais e pancre&aacute;ticas, cirrose hep&aacute;tica,    neoplasias de outros &oacute;rg&atilde;os, o CEA pode ser encontrado de forma    elevada, e em virtude disso, pacientes com tais caracter&iacute;sticas foram    exclu&iacute;dos do estudo<sup>9</sup>.</font></p>     <p><font size="2" face="Verdana">Neste estudo, em conson&acirc;ncia com os dados    de MANOUKIAN, BLUM (1991)<sup>10</sup>, o CEA mostrou eleva&ccedil;&atilde;o s&eacute;rica    em porcentagem semelhante (20%), fato que refor&ccedil;a o baixo valor diagn&oacute;stico,    posto que, isoladamente, n&atilde;o se mostrou &uacute;til em determinar a presen&ccedil;a    de doen&ccedil;a.</font></p>     <p><font size="2" face="Verdana">No entanto, KIM <i>et a</i>l (1995)<sup>11</sup>    publicaram trabalho que mostrava eleva&ccedil;&atilde;o dos n&iacute;veis s&eacute;ricos    pr&eacute;operat&oacute;rios de CEA, em aproximadamente 25% dos pacientes com    c&acirc;ncer g&aacute;strico, potencialmente ressec&aacute;veis<sup>12</sup>.</font></p>     <p><font size="2" face="Verdana">Portanto, tais resultados sugerem que os n&iacute;veis    de CEA s&eacute;rico n&atilde;o aumentam, significativamente, nos portadores    de c&acirc;ncer g&aacute;strico prim&aacute;rio, sugerindo incapacidade em predizer    o diagn&oacute;stico.</font></p>     <p><font size="2" face="Verdana">Por outro lado, o CEA se mostrou bom preditor    de normalidade dos linfonodos, compat&iacute;vel com os achados de TACHIBANA    <i>et al</i> (1998)<sup>13</sup> que, em estudo de 209 pacientes japoneses submetidos    &agrave; gastrectomia D2, relataram que pacientes CEA positivos tinham envolvimento    linfonodal mais freq&uuml;ente que os CEA negativos.</font></p>     <p><font size="2" face="Verdana">Esses fatos sugerem que, al&eacute;m do conhecido    valor na avalia&ccedil;&atilde;o de recorr&ecirc;ncia locorregional e sobrevida    a longo prazo, livre de doen&ccedil;a<sup>14</sup>, o CEA s&eacute;rico, quando positivo,    demonstra ser de utilidade como preditor de presen&ccedil;a de comprometimento    linfonodal.</font></p>     <p><font size="2" face="Verdana">Com rela&ccedil;&atilde;o aos pacientes com CEA    normal, 24 pacientes, 12 doentes (50%) tinham linfonodos comprometidos, isso    que dizer que, em metade dos casos com CEA normal pode haver possibilidade de    comprometimento linfonodal. Entretanto, dos 6 pacientes com CEA alterado, cinco    doentes (83,33%) apresentaram linfonodos comprometidos.</font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana">Com rela&ccedil;&atilde;o aos n&iacute;veis s&eacute;ricos    pr&eacute;-operat&oacute;rios de CEA e a classifica&ccedil;&atilde;o adotada    (UICC, 1998), dos 17 pacientes com linfonodos positivos, 14 foram estadiados    como N1(1 a 6 linfonodos positivos) e 3 como N2 (7 a 15 linfonodos positivos).    N&atilde;o foi encontrada signific&acirc;ncia estat&iacute;stica entre a eleva&ccedil;&atilde;o    s&eacute;rica pr&eacute;-operat&oacute;ria do CEA e o n&uacute;mero de linfonodos    acometidos.</font></p>     <p><font size="2" face="Verdana">Todos os pacientes submetidos a este estudo tiveram    o esp&eacute;cime cir&uacute;rgico analisado histologicamente atrav&eacute;s    da colora&ccedil;&atilde;o pela hematoxilina-eosina. Todavia, este tipo de exame    histol&oacute;gico convencional pode n&atilde;o diagnosticar micromet&aacute;stases    linfonodais, em que o foco &eacute; composto somente de poucas c&eacute;lulas    menores do que 2 mm de tamanho, com rea&ccedil;&atilde;o estromal envolt&oacute;ria    no linfonodo<sup>15</sup>.</font></p>     <p><font size="2" face="Verdana">Da mesma maneira, linfonodos negativos corados    pela hematoxilina-eosina podem apresentar microenvolvimento, ou seja, presen&ccedil;a    de c&eacute;lulas tumorais individuais no sinus ou na medula dos linfonodos    sem rea&ccedil;&atilde;o estromal ao redor<sup>16</sup>.</font></p>     <p><font size="2" face="Verdana">Neste estudo, n&atilde;o foi encontrado signific&acirc;ncia    estat&iacute;stica entre os valores de CEA s&eacute;rico pr&eacute;-operat&oacute;rio    e acometimento linfonodal, o que pode ser relacionado ao pequeno n&uacute;mero    da casu&iacute;stica, ou estadiamentos menos avan&ccedil;ados da doen&ccedil;a,    vez que nestes pacientes com acometimento linfonodal nas esta&ccedil;&otilde;es    13, 14, 15 e 16 foram considerados como met&aacute;stases &agrave; dist&acirc;ncia    e exclu&iacute;dos destes estudos<sup>17</sup>.</font></p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><b>CONCLUS&Otilde;ES</b></font></p>     <p><font size="2" face="Verdana">1. N&atilde;o foi observada correla&ccedil;&atilde;o    significante entre os n&iacute;veis s&eacute;ricos pr&eacute;-operat&oacute;rios    do CEA com o acometimento linfonodal regional em pacientes com c&acirc;ncer    g&aacute;strico, bem como com o n&uacute;mero de linfonodos comprometidos.</font></p>     <p><font size="2" face="Verdana">2. O CEA normal n&atilde;o inviabiliza a possibilidade    de acometimento linfonodal e, alterado, favorece a possibilidade da exist&ecirc;ncia    de linfonodos comprometidos.</font></p>     <p>&nbsp;</p>     <p><font size="3" face="Verdana"><b>REFER&Ecirc;NCIAS</b></font></p>     ]]></body>
<body><![CDATA[<!-- ref --><p><font size="2" face="Verdana">1. BARBUTO, J. A. M. - Marcadores tumorais. In:    BRENTANI, M. M.; COELHO, F. R. G.; IYEYASU, H.; KOWALSKI, L. P. editores. <i>Bases    da Oncologia</i>. 2<sup>a</sup> ed. S&atilde;o Paulo: Mavina; pg. 351-69, 1998.</font><!-- ref --><p><font size="2" face="Verdana">2. GOLD, P.; FREEDMAN, S. O. &#8211; Demonstration    of tumour-specific antigens in human colonic carcinomata by immunologic tolerance    and absorption techniques. <i>J. Exp. Med.</i>, 439-441, 1965.</font><!-- ref --><p><font size="2" face="Verdana">3. IKEDA, Y.; MORI, M.; KAJIYAMA, K.; KAMAKURA,    T.; MAEHARA, Y.; HARAGUCHI, Y.; HARAGUCHI, F. - Indicative value of carcinoembryonic    Antigen (CEA) for liver recurrence following curative ressection of stage II    and III gastric cancer. <i>Hepatogastroenterol.</i>, 43:1283-7, 1996.</font><!-- ref --><p><font size="2" face="Verdana">4. NOGUEIRA-COSTA, R. &amp; DUARTE, R. C. - O    uso de marcadores tumorais s&eacute;ricos no diagn&oacute;stico e tratamento    do c&acirc;ncer. <i>S.B.O.C.</i>, 2(1):35-49, 2000.</font><!-- ref --><p><font size="2" face="Verdana">5. AIKO, T.; SASAKO, M. The New Japonese classification    of Gastric Carcinoma: Points to be revised. <i>Gastric Cancer</i> , v.1, p.    15-30, 1998.</font><!-- ref --><p><font size="2" face="Verdana">6. MARRELLI, D.; ROVIELLO, F.; DE STEFANO, A.;    FARNETANI, M.; GAROSI, L.; MESSANO, A.; PINTO, E. - Prognostic significance    of CEA, CA 19-9 and CA 72-4 preoperative serum levels in gastric carcinoma.    <i>Oncology</i>, 57(1):55-62, 1999.</font><!-- ref --><p><font size="2" face="Verdana">7. BOLD, R.; OTA, D. M.; AJANI, J. A.; MANSFIELD,    P. F. - Peritoneal and serum tumor markers predict recurrence and survival of    patients with resectable gastric cancer. <i>Gastric Cancer</i>, 2(1):1-7, 1999.</font><!-- ref --><p><font size="2" face="Verdana">8. TOCCHI, A.; COSTA, G.; LEPRE, L.; LIOTTA,    G., MAZZONI, G.; CIANETTI, A. - The role of serum and gastric juice levels of    carcinoembryonic antigen, CA 19.9 and CA 72.4 in patients with gastric cancer.    <i>J. Cancer. Res. Clin. Oncol.</i>, 124(8):450-5, 1998.</font><!-- ref --><p><font size="2" face="Verdana">9. ANDREOLLO, N. A.; MORIOKA, C. Y.; LOPES, L.    R.; BRANDALISE, N. A.; TREVISAN, M. A.; LEONARDI, L. S. - O valor do ant&iacute;geno    carcinoembri&ocirc;nico (CEA) no diagn&oacute;stico do c&acirc;ncer g&aacute;strico.    <i>Rev. Col. Bras. Cirur.</i>, 21(4):198-202, 1994.</font><!-- ref --><p><font size="2" face="Verdana">10. MANOUKIAN, N.; BLUM, V. F. - CEA nos tumores    colorretais e g&aacute;stricos. <i>GED</i>, 10(2):41-3, 1991.</font><!-- ref --><p><font size="2" face="Verdana">11. KIM, Y. H.; AJANI, J. A.; OTA, D. M.; LYNCH,    P.; ROTH, J. A. - Value of serial carcinoembryonic antigen levels in patients    with resectable adenocarcinoma of the esofagus and stomach. <i>Cancer</i>, 15(2):451-6,    1995.</font><!-- ref --><p><font size="2" face="Verdana">12. GUENDELMANN, R. A. K.; SILVA, M. R.; LOUREN&Ccedil;O,    L.; FALC&Atilde;O, J. B.; MACHADO, D.; FORONES, N. M. &#8211; CA 72-4, CA 19-9    e CEA no c&acirc;ncer g&aacute;strico. <i>Compac. Gastroenterol.</i>, (6):9-10,    1995.</font><!-- ref --><p><font size="2" face="Verdana">13. TACHIBANA, M.; TAKEMOTO, Y.; NAKASHIMA, Y.;    KINUGASA, S.; KOTOH, T.; DHAR, D. K. - Serum carcinoembryonic antigen as a prognostic    factor in resectable gastric cancer. <i>J. Am. Coll. Surg.</i>, 187(1):64-8,    1998.</font><!-- ref --><p><font size="2" face="Verdana">14. KOCHI, M.; FUJII, M.; LANAMORI, N.; KAIGA,    T.; KAWAKAMI, T.; AIZAKI, K. - Evaluation of serum CEA and CA 19-9 levels as    prognostic factors in patients with gastric cancer. <i>Gastric Cancer</i>, 3(4):177-86,    2000.</font><!-- ref --><p><font size="2" face="Verdana">15. HERMANEK, P.; SOBIN, L. J. &#8211; UICC TNM    classification of malignant tumours. 4. ed. Springer: Berlim, rev 2, 1992.</font><!-- ref --><p><font size="2" face="Verdana">16. SIEWERT, J. R.; KESTEMEIER, R.; BUSCH, R.;    BOTTCHER, K.; RODER, J. D.; MULLER. J.; FELLBAUM, C.; HOFLER, H. &#8211; Benefits    of D2 lymphnode dissection for patients with gastric cancer and pN0 and pN1    lymphnode metastases. <i>J. Surgery</i>.; 83, 1144-7, 1996.</font><!-- ref --><p><font size="2" face="Verdana">17. UNI&Atilde;O INTERNACIONAL CONTRA O C&Acirc;NCER.    TNM &#8211; Classifica&ccedil;&atilde;o dos Tumores Malignos. 5.ed. Minist&eacute;rio    da Sa&uacute;de/Secretaria de Assist&ecirc;ncia &agrave; Sa&uacute;de/Instituto    Nacional de C&acirc;ncer. Rio de Janeiro. Brasil. 1998. 235p.</font><p>&nbsp;</p>     <p><font size="2" face="Verdana"><b><a name="endereco" id="endereco"></a><a href="#topo"><img src="/img/revistas/rpm/v20n4/seta.gif" border="0"></a>Endere&ccedil;o    para correspond&ecirc;ncia:    <br>   </b></font><font size="2" face="Verdana">Ant&ocirc;nio Carlos CHALU PACHECO<sup>1</sup>,        ]]></body>
<body><![CDATA[<br>   End: AV. Jos&eacute; Malcher 2271-S&atilde;o Braz     <br>   Tel: 91-3246-7484    <br>   Cel: 91-9982-3249</font></p>     <p><font size="2" face="Verdana">Isamu KOMATSU LIMA<sup>2</sup>,    <br>   End: Tv Mariz e Barros, 1319-Pedreira    <br>   Tel: 91-3226-6627    <br>   Cel: 91-8852-0730    <br>   e-mail: <a href="mailto:isamukomatsu@hotmail.com">isamukomatsu@hotmail.com</a></font></p>     <p><font size="2" face="Verdana">V&iacute;tor Moutinho da CONCEI&Ccedil;&Atilde;O    J&Uacute;NIOR<sup>3</sup>    <br>   End: Tv. Nove de julho 1051, apt. 900- S&atilde;o Braz    ]]></body>
<body><![CDATA[<br>   Cel: 91-8162-1428    <br>   e-mail : <a href="mailto:vitormoutinho@uol.com.br">vitormoutinho@uol.com.br</a></font></p>     <p><font size="2" face="Verdana">Recebido em 04.09.2009    <br>   Aprovado em 22.12.2006</font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font size="2" face="Verdana"><sup><a name="nota"></a><a href="#topo">1</a></sup>Trabalho    realizado no Hospital Ophir Loyola (HOL)- Servi&ccedil;o de Cancerologia Cir&uacute;rgica    </font></p>      ]]></body><back>
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