<?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>1646-2122</journal-id>
<journal-title><![CDATA[Revista Portuguesa de Ortopedia e Traumatologia]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Port. Ortop. Traum.]]></abbrev-journal-title>
<issn>1646-2122</issn>
<publisher>
<publisher-name><![CDATA[Sociedade Portuguesa de Ortopedia e Traumatologia]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1646-21222016000300005</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Episódios de derrame articular de repetição e gonalgia anterior em adolescente: Relato de caso de sinovite vilonodular pigmentada do joelho]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pinheiro]]></surname>
<given-names><![CDATA[Ana Costa]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Oliveira]]></surname>
<given-names><![CDATA[Carolina]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pombo]]></surname>
<given-names><![CDATA[Bruno]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Areias]]></surname>
<given-names><![CDATA[Margarida]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sousa]]></surname>
<given-names><![CDATA[Cristina]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gonzalez]]></surname>
<given-names><![CDATA[Francisca]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Unidade Local de Saúde do Alto Minho Serviço de Ortopedia e Traumatologia ]]></institution>
<addr-line><![CDATA[Viana do Castelo ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2016</year>
</pub-date>
<volume>24</volume>
<numero>3</numero>
<fpage>189</fpage>
<lpage>197</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S1646-21222016000300005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S1646-21222016000300005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S1646-21222016000300005&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[A sinovite vilonodular pigmentada (SVNP) do joelho constitui uma lesão tumoral singular caracterizada pela proliferação de células sinoviais, devendo esta entidade ser incluída no diagnóstico diferencial da gonalgia anterior. A SVNP do joelho é difícil de diagnosticar devido à sua raridade e localização intra-articular, possuindo a ressonância magnética uma função relevante. Os autores apresentam um caso clínico de SVNP do joelho em adolescente seguida na consulta externa de Ortopedia por gonalgia direita e episódios de derrame articular de repetição. A paciente foi submetida a ressecção artroscópica das lesões e sinovectomia. A cirurgia e o pós-operatório decorreram sem intercorrências, verificando-se o alívio da gonalgia e do derrame articular. Após 2 anos de follow-up não se registou evidência de recidiva. O objetivo deste trabalho é alertar a comunidade médica de que apesar de rara e de difícil diagnóstico, a SVNP do joelho, deve ser incluída no diagnóstico diferencial da dor anterior do joelho associada a episódios de derrame articular de repetição, nomeadamente nas crianças e adolescentes em crescimento. Os pacientes não tratados adequadamente podem evoluir para destruição articular, dai a importância do diagnóstico e tratamento atempado.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[The anterior knee pain is a common problem and a diagnostic and therapeutic challenge. Pigmented villonodular synovitis(PVNS) is a rare tumor lesion characterized by the proliferation of synovial cells and whose differential diagnosis must be included in the anterior knee pain. The synovial tumors are difficult to diagnose due to their rarity and intraarticular location, presenting magnetic resonance imaging an important role in their detection. The authors present a case of pigmented villonodular synovitis of the knee in an adolescent followed in orthopedic outpatient by right knee pain and recurrent joint effusion. She was submitted to arthroscopic lesions excision and synovectomy. Surgery and postoperative elapsed uneventful and there was relief from knee pain and strokes and there were no signs of recurrence. The aim of this study is to alert the medical community that although rare and difficult to diagnose, the PVNS of the knee, should be included in the differential diagnosis of anterior knee pain associated with recurrent joint effusion, particularly among children and adolescents. Patients not adequately treated can develop into joint destruction, hence the importance of diagnosis and timely treatment.]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[Joelho]]></kwd>
<kwd lng="pt"><![CDATA[adolescente]]></kwd>
<kwd lng="pt"><![CDATA[sinovite vilonodular pigmentada]]></kwd>
<kwd lng="pt"><![CDATA[tratamento]]></kwd>
<kwd lng="pt"><![CDATA[Artroscopia]]></kwd>
<kwd lng="en"><![CDATA[Knee]]></kwd>
<kwd lng="en"><![CDATA[adolescent]]></kwd>
<kwd lng="en"><![CDATA[pigmented villonodular synovitis]]></kwd>
<kwd lng="en"><![CDATA[treatment]]></kwd>
<kwd lng="en"><![CDATA[Arthroscopy]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="right"><b><font face="Verdana" size="2">CASO CLÍNICO</font></b></p>    <p>&nbsp;</p>    <p><b><font face="Verdana" size="4">Episódios de derrame articular de repetição e gonalgia anterior em adolescente - Relato de caso de sinovite vilonodular pigmentada do joelho</font></b></p>    <p>&nbsp;</p>    <p><font face="Verdana" size="2"><b>Ana Costa Pinheiro<sup>I</sup></b>; <b>Carolina Oliveira<sup>I</sup></b>; <b>Bruno Pombo<sup>I</sup></b>; <b>Margarida Areias<sup>I</sup></b>; <b>Cristina Sousa<sup>I</sup></b>; <b>Francisca Gonzalez<sup>I</sup></b></font></p>    <p><font face="Verdana" size="2">I. Serviço de Ortopedia e Traumatologia da Unidade Local de Saúde do Alto Minho, Viana do Castelo. Viana do Castelo.<br /></font></p>    <p>&nbsp;</p>    <p><font face="Verdana" size="2"><a name="topc"></a><a href="#c">Endereço para correspondência</a></font></p>    <p>&nbsp;</p>    <p><b><font face="Verdana" size="2">RESUMO</font></b></p><font face="verdana" size="2">    ]]></body>
<body><![CDATA[<p>A sinovite vilonodular pigmentada (SVNP) do joelho constitui uma les&atilde;o tumoral singular caracterizada pela prolifera&ccedil;&atilde;o de c&eacute;lulas sinoviais, devendo esta entidade ser inclu&iacute;da no diagn&oacute;stico diferencial da gonalgia anterior.</p>     <p>A SVNP do joelho &eacute; dif&iacute;cil de diagnosticar devido &agrave; sua raridade e localiza&ccedil;&atilde;o intra-articular, possuindo a resson&acirc;ncia magn&eacute;tica uma fun&ccedil;&atilde;o relevante.</p>     <p>Os autores apresentam um caso cl&iacute;nico de SVNP do joelho em adolescente seguida na consulta externa de Ortopedia por gonalgia direita e epis&oacute;dios de derrame articular de repeti&ccedil;&atilde;o. A paciente foi submetida a ressec&ccedil;&atilde;o artrosc&oacute;pica das les&otilde;es e sinovectomia. A cirurgia e o p&oacute;s-operat&oacute;rio decorreram sem intercorr&ecirc;ncias, verificando-se o al&iacute;vio da gonalgia e do derrame articular. Ap&oacute;s 2 anos de follow-up n&atilde;o se registou evid&ecirc;ncia de recidiva.</p>     <p>O objetivo deste trabalho &eacute; alertar a comunidade m&eacute;dica de que apesar de rara e de dif&iacute;cil diagn&oacute;stico, a SVNP do joelho, deve ser inclu&iacute;da no diagn&oacute;stico diferencial da dor anterior do joelho associada a epis&oacute;dios de derrame articular de repeti&ccedil;&atilde;o, nomeadamente nas crian&ccedil;as e adolescentes em crescimento. Os pacientes n&atilde;o tratados adequadamente podem evoluir para destrui&ccedil;&atilde;o articular, dai a import&acirc;ncia do diagn&oacute;stico e tratamento atempado.</p></font>    <p><font face="verdana" size="2"><b>Palavras chave</b>: Joelho, adolescente, sinovite vilonodular pigmentada, tratamento, Artroscopia. </font></p>    <p>&nbsp;</p>    <p><b><font face="Verdana" size="2">ABSTRACT</font></b></p><font face="verdana" size="2">    <p>The anterior knee pain is a common problem and a diagnostic and therapeutic challenge.</p>     <p>Pigmented villonodular synovitis(PVNS) is a rare tumor lesion characterized by the proliferation of synovial cells and whose differential diagnosis must be included in the anterior knee pain.</p>     <p>The synovial tumors are difficult to diagnose due to their rarity and intraarticular location, presenting magnetic resonance imaging an important role in their detection.</p>     ]]></body>
<body><![CDATA[<p>The authors present a case of pigmented villonodular synovitis of the knee in an adolescent followed in orthopedic outpatient by right knee pain and recurrent joint effusion. She was submitted to arthroscopic lesions excision and synovectomy.</p>     <p>Surgery and postoperative elapsed uneventful and there was relief from knee pain and strokes and there were no signs of recurrence.</p>     <p>The aim of this study is to alert the medical community that although rare and difficult to diagnose, the PVNS of the knee, should be included in the differential diagnosis of anterior knee pain associated with recurrent joint effusion, particularly among children and adolescents.</p>     <p>Patients not adequately treated can develop into joint destruction, hence the importance of diagnosis and timely treatment.<br /><br /></p></font>    <p><font face="verdana" size="2"><b>Key words</b>: Knee, adolescent, pigmented villonodular synovitis, treatment, Arthroscopy. </font></p>    <p>&nbsp;</p>    <p><b><font face="Verdana" size="2">INTRODUÇÃO</font></b></p><font face="verdana" size="2">    <p>A dor anterior do joelho constitui uma queixa comum, apresentando-se ainda como um desafio diagn&oacute;stico e terap&ecirc;utico<sup>1</sup>.</p>
    <p>A sinovite vilonodular pigmentada (SVNP) &eacute; definida como uma les&atilde;o tumoral invulgar caracterizada pela prolifera&ccedil;&atilde;o de c&eacute;lulas sinoviais e cujo diagn&oacute;stico diferencial deve ser inclu&iacute;do na gonalgia anterior<sup>2,3</sup>. Os tumores sinoviais do joelho s&atilde;o dif&iacute;ceis de diagnosticar devido &agrave; sua raridade e localiza&ccedil;&atilde;o intra-articular, apresentando a resson&acirc;ncia magn&eacute;tica nuclear (RMN) uma fun&ccedil;&atilde;o relevante<sup>4,5</sup>.</p>
    <p>A SVNP, tenossinovite vilonodular pigmentada e a bursite vilonodular pigmentada constituem um espectro de uma patologia rara, representada pela prolifera&ccedil;&atilde;o benigna da membrana sinovial das articula&ccedil;&otilde;es, ba&iacute;nhas tendinosas e bursas, respectivamente<sup>2,6,7</sup>.</p>
    ]]></body>
<body><![CDATA[<p>A SVNP &eacute; rara em crian&ccedil;as e adolescentes, sendo mais habitual em pacientes entre os 20 e os 50 anos. Esta entidade apresenta leve predile&ccedil;&atilde;o pelo sexo feminino<sup>8-11</sup>.</p>
    <p>A etiologia da SVNP n&atilde;o est&aacute; ainda designada, podendo estar relacionada a epis&oacute;dios de hemartrose de repeti&ccedil;&atilde;o, processo neopl&aacute;sico benigno, resposta a est&iacute;mulos desconhecidos ou a epis&oacute;dios de trauma repetitivos<sup>2,12</sup>.</p>
    <p>A SVNP pode atingir diversas articula&ccedil;&otilde;es, atingindo o joelho em 80% dos casos<sup>2,3</sup>. Esta entidade pode afigurar-se sob dois padr&otilde;es desiguais: a forma localizada (SVNPL) e a difusa (SVNPD), na qual a membrana sinovial da articula&ccedil;&atilde;o afetada &eacute; atingida parcial ou totalmente, respectivamente<sup>2,3</sup>. De referir que a SVNPL afigura-se, frequentemente, menos intensamente pigmentada e com menor prolifera&ccedil;&atilde;o vilosit&aacute;ria<sup>2</sup>.</p>
    <p>Os sintomas cl&iacute;nicos da SVNP dependem da localiza&ccedil;&atilde;o intra-articular ou extra-articular. A dor e o edema constituem os sintomas cl&iacute;nicos mais frequentemente associados ao tipo intraarticular<sup>2-4,10</sup>.</p>
    <p>O tratamento da SVNP assenta na ressec&ccedil;&atilde;o da les&atilde;o por via artrosc&oacute;pica e/ou aberta, todavia a recidiva local pode ocorrer em 18-46% dos casos<sup>4,10,12</sup>.</p>
    <p>Os autores apresentam um caso cl&iacute;nico de SVNP do joelho em adolescente seguida em consulta externa de ortopedia por gonalgia direita e epis&oacute;dios de derrame articular de repeti&ccedil;&atilde;o.</p>
    <p>O objetivo deste trabalho &eacute; alertar a comunidade m&eacute;dica de que apesar de rara e de dif&iacute;cil diagn&oacute;stico, a SVNP do joelho, deve ser inclu&iacute;da no diagn&oacute;stico diferencial da dor anterior do joelho associada a epis&oacute;dios de derrame articular de repeti&ccedil;&atilde;o, nomeadamente nas crian&ccedil;as e adolescentes em crescimento.</p></font>    <p>&nbsp;</p>    <p><b><font face="Verdana" size="2">RELATO DO CASO</font></b></p><font face="verdana" size="2">    <p>Paciente do sexo feminino, 14 anos, sem antecedentes patol&oacute;gicos de relevo, enviada a consulta externa por gonalgia &agrave; direita e epis&oacute;dios de derrame articular de repeti&ccedil;&atilde;o, sem hist&oacute;ria traum&aacute;tica aparente. A paciente referia dor na regi&atilde;o anterior do joelho direito de car&aacute;cter mec&acirc;nico, na aus&ecirc;ncia de &ldquo;falhas&rdquo; ou bloqueios. No exame objetivo apresentava hidrartrose moderada do joelho direito e dor &agrave; palpa&ccedil;&atilde;o da interlinha articular externa.</p>
    ]]></body>
<body><![CDATA[<p>N&atilde;o foram observados desvios de eixos, cicatrizes ou atrofias musculares. Foi ainda constatada a preserva&ccedil;&atilde;o das mobilidades ativas e a estabilidade anteroposterior e varo/valgo do joelho direito. As provas meniscais foram negativas. A radiografia simples do joelho nas incid&ecirc;ncias anteroposterior e perfil n&atilde;o manifestava anomalias (<a name="topf1"></a><a href="#f1">Figura 1</a>).</p>    <p>&nbsp;</p><a name="f1"></a>     <p>    <center><img src="/img/revistas/rpot/v24n3/24n3a05f1.jpg" width="389" height="299" border="0" /></center></p>    
<p>&nbsp;</p>
    <p>A RMN do joelho revelou uma forma&ccedil;&atilde;o nodular na regi&atilde;o intercondiliana, com cerca de 1.6cm, de maior eixo axial, apresentando um sinal interm&eacute;dio em T1, interm&eacute;dio/baixo sinal em T2, com perda de sinal nas sequ&ecirc;ncias de eco de gradiente. Tratava-se de uma les&atilde;o inespec&iacute;fica, que dado o seu comportamento deveria levar a considerar um processo de sinovite focal, com alguns focos de hemossiderina (com comportamento vilonodular ou n&atilde;o). O facto de n&atilde;o existirem calcifica&ccedil;&otilde;es, demonstradas no estudo radiogr&aacute;fico complementar, desfavorecia a possibilidade de se tratar de um condroma (<a name="topf1"></a><a href="#f1">Figuras 1</a> e <a name="topf2"></a><a href="#f2">2</a>).</p>    <p>&nbsp;</p><a name="f2"></a>     <p>    <center><img src="/img/revistas/rpot/v24n3/24n3a05f2.jpg" width="391" height="510" border="0" /></center></p>    
<p>&nbsp;</p>
    ]]></body>
<body><![CDATA[<p>A paciente foi submetida a excis&atilde;o cir&uacute;rgica das les&otilde;es (macroscopicamente avermelhadas/acastanhadas, da&iacute; a denomina&ccedil;&atilde;o sinovite pigmentada, devido &agrave; presen&ccedil;a da hemossiderina intra e extracelular) e sinovectomia do joelho por artroscopia. Durante o procedimento artrosc&oacute;pico foi visualizado o acometimento dos ligamentos cruzado anterior e posterior, sendo que os meniscos n&atilde;o estavam envolvidos (<a href="/img/revistas/rpot/v24n3/24n3a05f3.jpg">Figura 3</a>).</p>    
<p>&nbsp;</p>    <p>    <center><a href="/img/revistas/rpot/v24n3/24n3a05f3.jpg">Figura 3</a></center></p>    
<p>&nbsp;</p>
    <p>As les&otilde;es excisadas foram enviadas para estudo anatomopatol&oacute;gico (<a name="topf4"></a><a href="#f4">Figura 4</a>), que revelou tratase de les&otilde;es correspondentes a SVNP do joelho. (<a href="/img/revistas/rpot/v24n3/24n3a05f5.jpg">Figura 5</a>).</p>    
<p>&nbsp;</p><a name="f4"></a>     <p>    <center><img src="/img/revistas/rpot/v24n3/24n3a05f4.jpg" width="395" height="254" border="0" /></center></p>    
<p>&nbsp;</p>    ]]></body>
<body><![CDATA[<p>    <center><a href="/img/revistas/rpot/v24n3/24n3a05f5.jpg">Figura 5</a></center></p>    
<p>&nbsp;</p>
    <p>O exame histol&oacute;gico com hematoxilina e eosina demonstrou &aacute;reas de fibrose hialina e &aacute;reas de celularidade histiocit&aacute;ria com hemossiderina e cristais de colesterol (<a href="/img/revistas/rpot/v24n3/24n3a05f5.jpg">Figura 5.1- x2</a>). Observaram-se ainda c&eacute;lulas histiocit&aacute;rias espumosas (<a href="/img/revistas/rpot/v24n3/24n3a05f5.jpg">Figura 5.2- x20</a>) e c&eacute;lulas gigantes multinucleadas e c&eacute;lulas histiocit&aacute;rias mononucleares, com focos de hemossiderina (<a href="/img/revistas/rpot/v24n3/24n3a05f5.jpg">Figura 5.3- x40</a>).</p>
    
<p>O per&iacute;odo p&oacute;s-operat&oacute;rio decorreu sem intercorr&ecirc;ncias, tendo a paciente cumprido programa de reabilita&ccedil;&atilde;o funcional. A paciente foi orientada para Consulta Externa de Ortopedia. Ap&oacute;s 2 anos de seguimento, a doente permanece assintom&aacute;tica, sem limita&ccedil;&otilde;es nas atividades de vida di&aacute;ria e a RMN de controlo n&atilde;o revelou recidiva da les&atilde;o.</p></font>    <p>&nbsp;</p>    <p><b><font face="Verdana" size="2">DISCUSSÃO</font></b></p><font face="verdana" size="2">    <p>A n&iacute;vel mundial, a SVNP manifesta uma incid&ecirc;ncia global de 1.8 casos por milh&atilde;o de habitantes/ano, sendo uma condi&ccedil;&atilde;o excecional em crian&ccedil;as<sup>2,3,13</sup>.</p>
    <p>O mecanismo etiopatog&eacute;nico subjacente da SVNP permanece ainda obscuro, sendo os fatores gen&eacute;ticos particularmente importantes nos casos que acometem a inf&acirc;ncia<sup>2,12</sup>.</p>
    <p>Como atentado neste relato de caso, a SVNP &eacute; uma patologia monoarticular e de car&aacute;cter progressivo, acometendo principalmente as grandes articula&ccedil;&otilde;es, sendo o joelho implicado em 80% dos casos na forma difusa<sup>2,3</sup>.</p>
    ]]></body>
<body><![CDATA[<p>A sintomatologia, devido &agrave; sua inespecificidade, contribui, frequentemente, para o atraso no estabelecimento do diagn&oacute;stico, constituindo um desafio ainda maior na crian&ccedil;a em crescimento. A dor local, tumefa&ccedil;&atilde;o articular, massa palp&aacute;vel, rigidez articular, diminui&ccedil;&atilde;o da amplitude de movimento e instabilidade articular representam os achados cl&iacute;nicos mais frequentes<sup>2-4,10</sup>.</p>
    <p>O diagn&oacute;stico diferencial desta les&atilde;o tumoral intra-articular do joelho inclui desde a patologia neoformativa benigna &agrave; maligna, mormente o lipoma arborescens, o hemangioma sinovial, o neuroma plexiforme, a osteocondromatose sinovial, o quisto sinovial, o condroma e o osteocondroma, a patologia reumatismal e ainda a patologia infeciosa<sup>5,14-16</sup>.</p>
    <p>O diagn&oacute;stico da SVNP &eacute; realizado atrav&eacute;s da conjuga&ccedil;&atilde;o da hist&oacute;ria cl&iacute;nica, exame f&iacute;sico, imagiologia e exame histol&oacute;gico<sup>17-19</sup>.</p>
    <p>Como aconteceu no caso descrito, a radiografia &eacute; normal na maioria dos casos<sup>2</sup>. A RMN constitui o exame complementar de elei&ccedil;&atilde;o para o diagn&oacute;stico e acompanhamento desta entidade, pois possibilita discriminar as variadas estruturas intra-articulares e esclarecer as caracter&iacute;sticas e a extens&atilde;o das les&otilde;es de tecidos moles<sup>4,5</sup>. Como observado no caso apresentado, na RMN observam-se regi&otilde;es espec&iacute;ficas de baixo sinal nas sequ&ecirc;ncias ponderadas em T1 e T2 que correspondem ao dep&oacute;sito de hemossiderina dentro da sinovial<sup>14-16,18</sup>. Contudo, &eacute; de ressaltar que o diagn&oacute;stico irrevog&aacute;vel da SVNP &eacute; celebrado apenas pelo estudo histol&oacute;gico do tecido sinovial<sup>12</sup>.</p>
    <p>A paciente apresentada foi submetida a artroscopia para esclarecimento diagn&oacute;stico e para realiza&ccedil;&atilde;o de sinovectomia completa e excis&atilde;o das les&otilde;es. A histopatologia confirmou o diagn&oacute;stico de SVNP.</p>
    <p>Apesar da SVNP do joelho ser uma doen&ccedil;a rara e de dif&iacute;cil diagn&oacute;stico, particularmente nas crian&ccedil;as e adolescentes em crescimento, devemos ter em considera&ccedil;&atilde;o esta patologia nos pacientes com gonalgia anterior associada a epis&oacute;dios de derrame articular de repeti&ccedil;&atilde;o.</p>
    <p>Apesar da raridade, est&atilde;o descritos na literatura v&aacute;rios relatos de casos semelhantes ao caso apresentado, podendo as les&otilde;es ocorrer em qualquer local no interior da articula&ccedil;&atilde;o do joelho revestido com membrana sinovial, nomeadamente no ligamento cruzado posterior e ligamento cruzado anterior<sup>20-24</sup>.</p>
    <p>O tratamento da SVNP na forma nodular consta da sinovectomia enquanto na forma difusa esta pode exibir alta taxa de recorr&ecirc;ncia<sup>25-29</sup>.</p>
    <p>Os pacientes n&atilde;o tratados adequadamente podem evoluir para destrui&ccedil;&atilde;o articular, dai a import&acirc;ncia do diagn&oacute;stico e tratamento atempado<sup>25-29</sup>.</p>
    <p>Apesar de n&atilde;o ter sido realizada no caso descrito, este trabalho visa ainda alertar para a import&acirc;ncia da realiza&ccedil;&atilde;o de uma bi&oacute;psia pr&eacute;via que confirme o diagn&oacute;stico de SVNP, pois um diagn&oacute;stico incorreto pode conduzir a um tratamento inadequado e a um consequente desfecho fatal, sendo necess&aacute;rio excluir o diagn&oacute;stico de sarcoma epitelial prim&aacute;rio da sinovial do joelho, que poderia exigir uma amputa&ccedil;&atilde;o<sup>30</sup>. Opt&aacute;mos por realizar uma artroscopia do joelho com componente diagn&oacute;stico e terap&ecirc;utico, na medida em que se se diagnosticasse outra patologia no exame histol&oacute;gico que exigisse um tratamento mais agressivo do que o realizado, tratar&iacute;amos a patologia de acordo a <em>posteriori</em>.</p>
    ]]></body>
<body><![CDATA[<p>Apesar da escassez dos estudos, decorrente da baixa incid&ecirc;ncia desta les&atilde;o, acreditamos que a excis&atilde;o artrosc&oacute;pica das les&otilde;es caracter&iacute;sticas da SVNP associadas &agrave; sinovectomia constitui um m&eacute;todo efetivo, de baixa morbilidade, proporcionando a remiss&atilde;o dos sintomas e apresentando baixo &iacute;ndice de recidiva, tal como verificado no caso em estudo.</p></font>    <p>&nbsp;</p>    <p><b><font face="Verdana" size="2">REFERÊNCIAS BIBLIOGRÁFICAS</font></b></p>    <p><font face="verdana" size="2">1. Post WR. Anterior Knee Pain: Diagnosis and Treatment. J Am Acad Orthop Surg. 2005 Dec; 13 (8): 534-543</font></p>    <p><font face="verdana" size="2">2. Bouali H, Deppert EJ, Leventhal LJ, Reeves B, Pope T. Pigmented villonodular synovitis: a disease in evolution. J Rheumatol. 2004 Aug; 31 (8): 1659-1662</font></p>    <p><font face="verdana" size="2">3. BBojanic I, Ivkovic A, Dotlic S, Ivkovic M, Manojlovic S. Localized pigmented villonodular synovitis of the knee: diagnostic challenge and arthroscopic treatment:a report of three cases. Knee Surg Sports Traumatol Arthrosc. 2001 Nov; 9 (6): 350-354</font></p>    <p><font face="verdana" size="2">4. Dürr HR, Stäbler A, Maier M, Refior HJ. Pigmented villonodular synovitis. Review of 20 cases. J Rheumatol. 2001 Jul; 28 (7): 1620-1630</font></p>    <p><font face="verdana" size="2">5. Goldman AB, DiCarlo EF. Pigmented villonodular synovitis. Diagnosis and differential diagnosis. Radiol Clin North Am. 1988 Nov; 26 (6): 1327-1347</font></p>    <p><font face="verdana" size="2">6. Granowitz SP, D'Antonio J, Mankin HL. The pathogenesis and long-term end results of pigmented villonodular synovitis. Clin Orthop Relat Res. 1976 Jan;  (114): 335-351</font></p>    <p><font face="verdana" size="2">7. Myers BW, Masi AT. Pigmented villonodular synovitis and tenosynovitis: a clinical epidemiologic study of 166 cases and literature review. Medicine (Baltimore). 1980 May; 59 (3): 223-238</font></p>    ]]></body>
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Chiffolot X, Ehlinger M, Bonnomet F, Kempf JF. Arthroscopic resection of pigmented villonodular synovitis pseudotumor of the shoulder: a case report with three year follow-up.. Rev Chir Orthop Reparatrice Appar Mot. 2005; 91 (5): 470-475</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1312846&pid=S1646-2122201600030000500029&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><font face="verdana" size="2">30. Chow LTC. Primary synovial epithelioid sarcoma of the knee: distinctly unusual location leading to its confusion with pigmented villonodular synovitis. APMIS. 2015; 123: 350-358</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1312847&pid=S1646-2122201600030000500030&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><p>&nbsp;</p>    <p><b><font face="Verdana" size="2">Conflito de interesse: </font></b></p><font face="verdana" size="2">    <p>Nada a declarar</p></font>    <p>&nbsp;</p><a name="c"></a>    <p><b><font face="Verdana" size="2"><a href="#topc">Endereço para correspondência</a></font></b></p>    <p><font face="Verdana" size="2">Ana Costa Pinheiro    <br>Serviço de Ortopedia e Traumatologia    ]]></body>
<body><![CDATA[<br>Unidade Local de Saúde do Alto Minho    <br>Estrada de Santa Luzia    <br>4901-858 Viana do Castelo    <br>Telefone: 91 433 58 60    <br><a href="mailto:ana.alexandra.pinheiro@gmail.com">ana.alexandra.pinheiro@gmail.com</a></font></p>    <p>&nbsp;</p>    <p><font face="verdana" size="2"><b>Data de Submissão: </b> 2015-12-03</font></p>    <p><font face="verdana" size="2"><b>Data de Revisão: </b> 2017-01-15</font></p>    <p><font face="verdana" size="2"><b>Data de Aceitação: </b> 2017-02-27</font></p>     ]]></body><back>
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