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<article xmlns:xlink="http://www.w3.org/1999/xlink" specific-use="sps-1.9" dtd-version="1.1" xml:lang="pt" article-type="case-report">
  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">abc</journal-id>
      <journal-title-group>
        <journal-title>Arquivos Brasileiros de Cardiologia</journal-title>
        <abbrev-journal-title abbrev-type="publisher">Arq. Bras. Cardiol.</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">0066-782X</issn>
      <issn pub-type="epub">1678-4170</issn>
      <publisher>
        <publisher-name>Sociedade Brasileira de Cardiologia - SBC</publisher-name>
        <publisher-loc>S&#227;o Paulo, SP, Brazil</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v3">PkqGGwvDQ7rX65xfXWzCRWj</article-id>
      <article-id pub-id-type="other">00017</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2011001500017</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(11)09700617</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2011001500017</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Relato de Caso</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Taquicardia ventricular associada com linfoma n&#227;o-Hodgkin</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Chemello</surname>
            <given-names>Diego</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Raupp-da-Rosa</surname>
            <given-names>Priscila</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Tel&#243;</surname>
            <given-names>Guilherme</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Clausell</surname>
            <given-names>Nadine</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="city">Porto Alegre</named-content>
          <named-content content-type="state">Rio Grande do Sul</named-content>
        </addr-line>
        <institution content-type="orgname">Universidade Federal do Rio Grande do Sul</institution>
        <institution content-type="orgdiv1">Hospital de Cl&#237;nicas de Porto Alegre </institution>
        <country country="BR">Brazil</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>12</month>
        <year>2011</year>
      </pub-date>
      <volume>97</volume>
      <issue>6</issue>
      <fpage>e132</fpage>
      <lpage>e134</lpage>
      <history>
        <date date-type="received">
          <day>01</day>
          <month>08</month>
          <year>2010</year>
        </date>
        <date date-type="rev-recd">
          <day>11</day>
          <month>10</month>
          <year>2010</year>
        </date>
        <date date-type="accepted">
          <day>10</day>
          <month>11</month>
          <year>2011</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/4.0/" xml:lang="en">
          <license-p>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</license-p>
        </license>
      </permissions>
      <abstract>
        <p>Linfoma n&#227;o-Hodgkin sist&#234;mico pode afetar o mioc&#225;rdio, particularmente em pacientes imunocomprometidos. Quando presentes, sinais e sintomas s&#227;o geralmente inespec&#237;ficos, tornando o diagn&#243;stico de envolvimento card&#237;aco muito dif&#237;cil antes da aut&#243;psia. Arritmias ventriculares tamb&#233;m s&#227;o pouco usuais nesse cen&#225;rio. Descrevemos um caso de linfoma n&#227;o-Hodgkin mioc&#225;rdico secund&#225;rio, que se apresentou com taquicardia ventricular monom&#243;rfica sustentada e espessamento do septo interventricular basal. Completa remiss&#227;o das les&#245;es mioc&#225;rdicas foi observada ap&#243;s o t&#233;rmino da quimioterapia de segunda linha, sem recorr&#234;ncias posteriores de arritmias em oito meses.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>Taquicardia ventricular</kwd>
        <kwd>neoplasias card&#237;acas</kwd>
        <kwd>doen&#231;a de Hodgkin</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>16</day>
        <month>01</month>
        <year>2012</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>
      <bold>RELATO DE CASO</bold>
    </p>
    <p>
      <bold>Taquicardia ventricular associada com linfoma n&#227;o-Hodgkin</bold>
    </p>
    <p>
      <bold>Diego Chemello; Priscila Raupp-da-Rosa; Guilherme Tel&#243;; Nadine Clausell</bold>
    </p>
    <p>Hospital de Cl&#237;nicas de Porto Alegre - Universidade Federal do Rio Grande do Sul, Porto Alegre, RS - Brasil</p>
    <p>
      <xref ref-type="corresp" rid="end">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p>Linfoma n&#227;o-Hodgkin sist&#234;mico pode afetar o mioc&#225;rdio, particularmente em pacientes imunocomprometidos. Quando presentes, sinais e sintomas s&#227;o geralmente inespec&#237;ficos, tornando o diagn&#243;stico de envolvimento card&#237;aco muito dif&#237;cil antes da aut&#243;psia. Arritmias ventriculares tamb&#233;m s&#227;o pouco usuais nesse cen&#225;rio. Descrevemos um caso de linfoma n&#227;o-Hodgkin mioc&#225;rdico secund&#225;rio, que se apresentou com taquicardia ventricular monom&#243;rfica sustentada e espessamento do septo interventricular basal. Completa remiss&#227;o das les&#245;es mioc&#225;rdicas foi observada ap&#243;s o t&#233;rmino da quimioterapia de segunda linha, sem recorr&#234;ncias posteriores de arritmias em oito meses.</p>
    <p><bold>Palavras-chave:</bold> Taquicardia ventricular, neoplasias card&#237;acas, doen&#231;a de Hodgkin.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>O envolvimento card&#237;aco secund&#225;rio &#224; met&#225;stase de tumores malignos &#233; relativamente incomum. Estudos de aut&#243;psias mostraram uma incid&#234;ncia de at&#233; 12% de envolvimento card&#237;aco em todos os pacientes com malignidade e maioria deles &#233; assintom&#225;tica. </p>
    <p>Linfoma n&#227;o-Hodgkin (LNH) sist&#234;mico &#233; uma doen&#231;a que pode afetar o mioc&#225;rdio, particularmente em pacientes imunocomprometidos. A apresenta&#231;&#227;o cl&#237;nica geralmente &#233; inespec&#237;fica. O diagn&#243;stico de envolvimento card&#237;aco pode ser dif&#237;cil e requer alto grau de suspeita cl&#237;nica. Arritmias ventriculares s&#227;o extremamente incomuns e apenas alguns casos foram descritos at&#233; hoje. Essas arritmias geralmente s&#227;o sintom&#225;ticas e est&#227;o associadas com instabilidade hemodin&#226;mica significativa. </p>
    <p>
      <bold>Relato de caso</bold>
    </p>
    <p>Uma paciente de 27 anos, do sexo feminino, apresentou-se ao pronto socorro com palpita&#231;&#245;es de in&#237;cio s&#250;bito e desconforto tor&#225;cico. A press&#227;o arterial (PA) era de 68 x 40 mmHg e a frequ&#234;ncia card&#237;aca (FC) era de 184 bpm. Ao exame f&#237;sico, a paciente apresentava aumento de volume da mama esquerda e massa abdominal difusa. O eletrocardiograma (ECG) de 12 deriva&#231;&#245;es realizado na admiss&#227;o revelou taquicardia de complexo alargado com padr&#227;o de bloqueio de ramo esquerdo e concord&#226;ncia negativa nos eletrodos precordiais (<xref ref-type="fig" rid="a17fig01">Figura 1A</xref>).</p>
    <p><fig id="a17fig01"/>&#13;
&#160;&#13;
</p>
    <p>
      <fig id="a17fig01a">
        <graphic xlink:href="1678-4170-abc-97-06-e132-00017-gf01.jpg"/></fig>
    </p>
    <p>&#13;
  <fig id="a17fig01xfig1b"/><fig id="a17fig01b"><graphic xlink:href="1678-4170-abc-97-06-e132-00017-gf02.jpg"/></fig></p>
    <p>Com base na apresenta&#231;&#227;o inicial, o diagn&#243;stico de taquicardia ventricular monom&#243;rfica foi estabelecido e a paciente foi submetida &#224; cardiovers&#227;o el&#233;trica resultando em ritmo sinusal normal. O ECG foi repetido e mostrou ritmo sinusal normal, sem altera&#231;&#245;es do segmento ST (<xref ref-type="fig" rid="a17fig01">Figura 1B</xref>). A paciente recebeu uma infus&#227;o intravenosa de amiodarona e ent&#227;o foi admitida na Unidade de Terapia Intensiva (UTI). A investiga&#231;&#227;o foi negativa para isquemia mioc&#225;rdica ou embolia pulmonar. Uma ecocardiografia transtor&#225;cica (ETT) revelou fun&#231;&#245;es ventriculares esquerda e direita normais, derrame peric&#225;rdico posterior difuso e espessamento do mioc&#225;rdio basal-septal, que n&#227;o estava presente em exame anterior realizado um ano antes, para investiga&#231;&#227;o de dispn&#233;ia durante atividade f&#237;sica (<xref ref-type="fig" rid="a17fig02m">Figura 2A</xref>). A investiga&#231;&#227;o cl&#237;nica revelou um hist&#243;rico m&#233;dico de s&#237;ndrome de imunodefici&#234;ncia adquirida (AIDS) devido &#224; infec&#231;&#227;o pelo v&#237;rus da imunodefici&#234;ncia humana (HIV) nos 12 meses anteriores e contagem inicial de CD4 de 39 c&#233;lulas/mm<sup>3</sup>. Imediatamente ap&#243;s esse diagn&#243;stico, a paciente iniciou tratamento com terapia antiretroviral altamente ativa (HAART), o que aumentou e estabilizou a contagem de CD4 em 89 c&#233;lulas/mm<sup>3</sup> ap&#243;s tr&#234;s meses de tratamento. Ela tamb&#233;m recebeu o diagn&#243;stico de linfoma difuso de grandes c&#233;lulas B (LDGCB), um linfoma n&#227;o-Hodgkin que foi inicialmente tratado com uma combina&#231;&#227;o de ciclofosfamida, adriamicina, vincristina e prednisona (CHOP). Devido &#224; neutropenia grave, o tratamento foi mudado para Etoposide, Vincristina, Doxorrubicina, Ciclofosfamida e Prednisona (EPOCH). Apesar do curso completo de tratamento, a remiss&#227;o do linfoma n&#227;o foi atingida (bi&#243;psia de tecido da mama e massa retroperitoneal foi positiva para (LDGCB). Na semana ap&#243;s a admiss&#227;o no pronto socorro, a paciente come&#231;ou a receber Ifosfamida, Carboplatina e Etoposide (ICE), um protocolo de quimioterapia de segunda linha. </p>
    <p content-type="asset">
      <fig id="a17fig02m">
        <graphic xlink:href="1678-4170-abc-97-06-e132-00017-gf03.jpg"/></fig>
    </p>
    <p>Ap&#243;s consulta com a Oncologia, a quimioterapia com o protocolo ICE para LDGCB foi mantido. A bi&#243;psia card&#237;aca foi considerada, o que a paciente recusou. Um novo ETT ap&#243;s 30 dias de quimioterapia revelou melhora acentuada, com diminui&#231;&#227;o do derrame peric&#225;rdico, bem como completa redu&#231;&#227;o do espessamento septal mioc&#225;rdico (<xref ref-type="fig" rid="a17fig02m">Figura 2B</xref>). Nenhuma arritmia adicional foi documentada nos oito meses seguintes. Nenhum medicamento anti-arr&#237;tmico cr&#244;nico foi prescrito. </p>
    <p>
      <bold>Discuss&#227;o</bold>
    </p>
    <p>O envolvimento metast&#225;tico do cora&#231;&#227;o &#233; descoberto na aut&#243;psia em 10 a 12% dos pacientes com malignidades, mais frequentemente de carcinoma pulmonar. A maioria desses casos envolve o peric&#225;rdio e o epic&#225;rdio, sugerindo uma invas&#227;o linf&#225;tica regional. O envolvimento mioc&#225;rdico &#233; menos frequente e geralmente associado com melanoma ou linfoma, sugerindo invas&#227;o hemat&#243;gena. Linfoma difuso de grandes c&#233;lulas B (LDGCB) &#233; um linfoma n&#227;o-Hodgkin (LNH) com incid&#234;ncia em indiv&#237;duos infectados pelo HIV de mais de 100 vezes a incid&#234;ncia na popula&#231;&#227;o em geral<sup>1</sup>. </p>
    <p>Em pacientes com LNH, sinais cl&#237;nicos de envolvimento card&#237;aco s&#227;o inespec&#237;ficos e frequentemente n&#227;o s&#227;o detectados antes da morte. Dor tor&#225;cica, insufici&#234;ncia card&#237;aca congestiva e derrame peric&#225;rdico foram relatados anteriormente, sendo o &#250;ltimo a apresenta&#231;&#227;o mais comum<sup>2</sup>. Embora v&#225;rios casos de arritmias tenham sido documentados, a maioria inclui bloqueio atrioventricular, provavelmente relacionado &#224; les&#227;o secund&#225;ria do sistema de condu&#231;&#227;o<sup>3</sup>. Arritmias ventriculares s&#227;o raramente diagnosticadas nessa popula&#231;&#227;o. Por raz&#245;es desconhecidas, a maioria dos casos foi relatada em pacientes com linfoma card&#237;aco prim&#225;rio<sup>4,5</sup>.</p>
    <p>Descrevemos um caso de envolvimento card&#237;aco de LNH, que apresentou taquicardia ventricular monom&#243;rfica, a qual &#233; uma manifesta&#231;&#227;o rara. O diagn&#243;stico foi realizado com base em estudos de imagem obtidos atrav&#233;s de ecocardiograma transtor&#225;cico, que &#233; um m&#233;todo barato e facilmente dispon&#237;vel. &#201; importante enfatizar que em tais casos, o envolvimento card&#237;aco pode ser melhor determinado com modalidades de estudo de imagem mais sens&#237;veis, como a resson&#226;ncia magn&#233;tica ou a tomografia computadorizada. Entretanto, esses m&#233;todos s&#227;o caros e nem sempre est&#227;o dispon&#237;veis em centros card&#237;acos. O mecanismo associado com a taquicardia ventricular (TV) poderia ser secund&#225;rio ao atraso na condu&#231;&#227;o ventricular causado por invas&#227;o mioc&#225;rdica localizada de c&#233;lulas do linfoma, embora a atividade desencadeada n&#227;o possa ser exclu&#237;da. Nesse cen&#225;rio, o estudo eletrofisiol&#243;gico pode ser uma ferramenta valiosa em casos selecionados para entender os mecanismos de arritmia e a resposta ao tratamento farmacol&#243;gico. Entretanto, nenhum estudo prospectivo testando o papel dessa modalidade est&#225; dispon&#237;vel nessa popula&#231;&#227;o. </p>
    <p>&#201; poss&#237;vel considerar a hip&#243;tese de que o recente tratamento quimioter&#225;pico causou a toxicidade mioc&#225;rdica e desencadeou a TV, j&#225; que dois casos de TV foram anteriormente documentados com o uso de Ifosfamida<sup>6</sup>. Entretanto, essa hip&#243;tese &#233; menos favorecida devido &#224; melhora dos implantes metast&#225;ticos nos dias subsequentes com o protocolo ICE. </p>
    <p>Em conclus&#227;o, relatamos um caso pouco usual de envolvimento card&#237;aco de LNH com TV. A ocorr&#234;ncia de arritmias nessa popula&#231;&#227;o sempre deve alertar para a possibilidade de envolvimento metast&#225;tico no mioc&#225;rdio. </p>
    <p>
      <bold>Potencial Conflito de Interesses</bold>
    </p>
    <p>Declaro n&#227;o haver conflito de interesses pertinentes.</p>
    <p>
      <bold>Fontes de Financiamento</bold>
    </p>
    <p>O presente estudo n&#227;o teve fontes de financiamento externas.</p>
    <p>
      <bold>Vincula&#231;&#227;o Acad&#234;mica</bold>
    </p>
    <p>Este artigo &#233; parte de tese de Doutorado de Diego Chemello pelo Hospital de Cl&#237;nicas de Porto Alegre - Universidade Federal do Rio Grande do Sul.</p>
    <p>
      <fn id="end" fn-type="corresp">
        <label>
          <bold>Correspond&#234;ncia:</bold>
        </label>
        <p> Nadine Clausell </p>
        <p> Rua Ramiro Barcelos 2350, Sala 2061 </p>
        <p> 90035-003 - Porto Alegre, RS - Brasil </p>
        <p> E-mail: </p>
        <p>
          <email xlink:href="clausell@portoweb.com.br">clausell@portoweb.com.br</email>
        </p>
      </fn>
    </p>
    <p>Artigo recebido em 01/08/10; revisado recebido em 11/10/10; aceito em 11/11/10.</p>
  </body>
  <back>
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          <article-title>High-dose ifosfamide is associated with severe, reversible cardiac dysfunction</article-title>
          <source>Ann Intern Med</source>
          <date>
            <year>1993</year>
          </date>
          <fpage>31</fpage>
          <lpage>6</lpage>
          <issue>1</issue>
          <volume>118</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Quezado</surname>
              <given-names>ZM</given-names>
            </name>
            <name>
              <surname>Wilson</surname>
              <given-names>WH</given-names>
            </name>
            <name>
              <surname>Cunnion</surname>
              <given-names>RE</given-names>
            </name>
            <name>
              <surname>Parker</surname>
              <given-names>MM</given-names>
            </name>
            <name>
              <surname>Reda</surname>
              <given-names>D</given-names>
            </name>
            <name>
              <surname>Bryant</surname>
              <given-names>G</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
    </ref-list>
  </back>
  <sub-article article-type="translation" id="TRes" xml:lang="es">
    <front-stub>
      <article-categories/>
      <title-group>
        <article-title xml:lang="es">Taquicardia ventricular asociada con linfoma no Hodgkin</article-title>
      </title-group>
      <abstract xml:lang="es">
        <p>Linfoma no Hodgkin sist&#233;mico puede afectar el miocardio, particularmente en pacientes inmunocomprometidos. Cuando est&#225;n presentes, se&#241;ales y s&#237;ntomas son generalmente inespec&#237;ficos, volviendo el diagn&#243;stico de compromiso card&#237;aco muy dif&#237;cil antes de la autopsia. Arritmias ventriculares tambi&#233;n son poco usuales en ese escenario. Describimos un caso de linfoma no Hodgkin mioc&#225;rdico secundario, que se present&#243; con taquicardia ventricular monom&#243;rfica sustentada y engrosamiento del septo interventricular basal. Completa remisi&#243;n de las lesiones mioc&#225;rdicas fue observada despu&#233;s del t&#233;rmino de la quimioterapia de segunda l&#237;nea, sin recurrencias posteriores de arritmias en ocho meses.</p>
      </abstract>
      <kwd-group xml:lang="es">
        <kwd>Taquicardia ventricular</kwd>
        <kwd>neoplasias card&#237;acas</kwd>
        <kwd>enfermedad de Hodgkin</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>CASO CL&#205;NICO</bold>
      </p>
      <p>
        <fn id="enda-body2">
          <label>
            <bold>Taquicardia ventricular asociada con linfoma no Hodgkin</bold>
          </label>
          <p>
            <bold>Diego Chemello; Priscila Raupp-da-Rosa; Guilherme Tel&#243;; Nadine Clausell</bold>
          </p>
        </fn>
      </p>
      <p>Hospital de Cl&#237;nicas de Porto Alegre - Universidade Federal do Rio Grande do Sul, Porto Alegre, RS - Brasil</p>
      <p>Correspondencia</p>
      <p>
        <bold>RESUMEN</bold>
      </p>
      <p>Linfoma no Hodgkin sist&#233;mico puede afectar el miocardio, particularmente en pacientes inmunocomprometidos. Cuando est&#225;n presentes, se&#241;ales y s&#237;ntomas son generalmente inespec&#237;ficos, volviendo el diagn&#243;stico de compromiso card&#237;aco muy dif&#237;cil antes de la autopsia. Arritmias ventriculares tambi&#233;n son poco usuales en ese escenario. Describimos un caso de linfoma no Hodgkin mioc&#225;rdico secundario, que se present&#243; con taquicardia ventricular monom&#243;rfica sustentada y engrosamiento del septo interventricular basal. Completa remisi&#243;n de las lesiones mioc&#225;rdicas fue observada despu&#233;s del t&#233;rmino de la quimioterapia de segunda l&#237;nea, sin recurrencias posteriores de arritmias en ocho meses.</p>
      <p><bold>Palabras clave:</bold> Taquicardia ventricular, neoplasias card&#237;acas, enfermedad de Hodgkin.</p>
      <p>
        <bold>Introducci&#243;n</bold>
      </p>
      <p>El compromiso card&#237;aco secundario a la met&#225;stasis de tumores malignos es relativamente infrecuente. Estudios de autopsias mostraron una incidencia de hasta 12% de compromiso card&#237;aco en todos los pacientes con malignidad y mayor&#237;a de ellos es asintom&#225;tica. </p>
      <p>Linfoma no Hodgkin (LNH) sist&#233;mico es una enfermedad que puede afectar el miocardio, particularmente en pacientes inmunocomprometidos. La presentaci&#243;n cl&#237;nica generalmente es inespec&#237;fica. El diagn&#243;stico de compromiso card&#237;aco puede ser dif&#237;cil y requiere alto grado de sospecha cl&#237;nica. Arritmias ventriculares son extremadamente infrecuentes y apenas algunos casos fueron descritos hasta hoy. Esas arritmias generalmente son sintom&#225;ticas y est&#225;n asociadas con inestabilidad hemodin&#225;mica significativa. </p>
      <p>
        <bold>Relato de caso</bold>
      </p>
      <p>Una paciente de 27 a&#241;os, del sexo femenino, se present&#243; en la Sala de Emergencias con palpitaciones de inicio s&#250;bito y disconfort tor&#225;cico. La presi&#243;n arterial (PA) era de 68 x 40 mmHg y la frecuencia card&#237;aca (FC) era de 184 lpm. Al examen f&#237;sico, la paciente presentaba aumento de volumen de la mama izquierda y masa abdominal difusa. El electrocardiograma (ECG) de 12 derivaciones realizado en la admisi&#243;n revel&#243; taquicardia de complejo ensanchado con est&#225;ndar de bloqueo de ramo izquierdo y concordancia negativa en los electrodos precordiales (<xref ref-type="fig" rid="es_a17fig01-body2">Figura 1A</xref>).</p>
      <p content-type="html"><fig id="es_a17fig01-body2"><graphic xlink:href="https://minio.scielo.br/documentstore/1678-4170/PkqGGwvDQ7rX65xfXWzCRWj/a5c0247b095f0b87f58df3010faf98ecb2bee79c.jpg"/><graphic xlink:href="1678-4170-abc-97-06-e132-00017-gf01-es.jpg"/></fig>&#13;
&#160;&#13;
</p>
      <p>Con base en la presentaci&#243;n inicial, el diagn&#243;stico de taquicardia ventricular monom&#243;rfica fue establecido y la paciente fue sometida a cardioversi&#243;n el&#233;ctrica para el ritmo sinusal normal. El ECG fue repetido y mostr&#243; ritmo sinusal normal, sin alteraciones del segmento ST (<xref ref-type="fig" rid="es_a17fig01-body2">Figura 1B</xref>). La paciente recibi&#243; una infusi&#243;n intravenosa de amiodarona y entonces fue admitida en la Unidad de Terapia Intensiva (UTI). La investigaci&#243;n fue negativa para isquemia mioc&#225;rdica o embolia pulmonar. Una ecocardiograf&#237;a transtor&#225;cica (ETT) revel&#243; funciones ventriculares izquierda y derecha normales, derrame peric&#225;rdico posterior difuso y engrosamiento del miocardio basal-septal, que no estaba presente en examen anterior realizado un a&#241;o antes para investigaci&#243;n de disnea durante actividad f&#237;sica (<xref ref-type="fig" rid="es_a17fig02m-body2">Figura 2A</xref>). La investigaci&#243;n cl&#237;nica revel&#243; un hist&#243;rico m&#233;dico de s&#237;ndrome de inmunodeficiencia adquirida (SIDA) debido a infecci&#243;n por virus de inmunodeficiencia humana (VIH) en los 12 meses anteriores y conteo inicial de CD4 de 39 c&#233;lulas/mm<sup>3</sup>. Inmediatamente despu&#233;s de ese diagn&#243;stico, la paciente inici&#243; tratamiento con terapia antiretroviral altamente activa (HAART), lo que aument&#243; y estabiliz&#243; el conteo de CD4 en 89 c&#233;lulas/mm<sup>3</sup> despu&#233;s de tres meses de tratamiento. Tambi&#233;n recibi&#243; el diagn&#243;stico de linfoma difuso de grandes c&#233;lulas B (LDGCB), un linfoma no Hodgkin que fue inicialmente tratado con una combinaci&#243;n de ciclofosfamida, adriamicina, vincristina y prednisona (CHOP). Debido a la neutropenia grave, el tratamiento fue cambiado a Etoposide, Vincristina, Doxorrubicina, Ciclofosfamida y Prednisona (EPOCH). A pesar del curso completo de tratamiento, la remisi&#243;n del linfoma no fue alcanzada (biopsia de tejido de la mama y masa retroperitoneal fue positiva para (LDGCB). En la semana despu&#233;s de la admisi&#243;n en Sala de Emergencia, la paciente comenz&#243; a recibir Ifosfamida, Carboplatina y Etoposide (ICE), un protocolo de quimioterapia de segunda l&#237;nea.</p>
      <p content-type="asset">
        <fig id="es_a17fig02m-body2">
          <graphic xlink:href="1678-4170-abc-97-06-e132-00017-gf02-es.jpg"/></fig>
      </p>
      <p>Despu&#233;s de consulta con Oncol&#243;g&#237;a, la quimioterapia con el protocolo ICE para LDGCB fue mantenida. La biopsia card&#237;aca fue considerada, lo que la paciente rechaz&#243;. Un nuevo ETT despu&#233;s de 30 d&#237;as de quimioterapia revel&#243; mejora acentuada, con disminuci&#243;n del derrame peric&#225;rdico, as&#237; como completa reducci&#243;n del engrosamiento septal mioc&#225;rdico (<xref ref-type="fig" rid="es_a17fig02m-body2">Figura 2B</xref>). Ninguna arritmia adicional fue documentada en los ocho meses siguientes. Ning&#250;n medicamento antiarr&#237;tmico cr&#243;nico fue prescripto. </p>
      <p>
        <bold>Discusi&#243;n</bold>
      </p>
      <p>El compromiso metast&#225;tico del coraz&#243;n es descubierto en la autopsia en 10 a 12% de los pacientes con malignidades, m&#225;s frecuentemente de carcinoma pulmonar. La mayor&#237;a de esos casos envuelve el pericardio y el epicardio, sugiriendo una invasi&#243;n linf&#225;tica regional. El compromiso mioc&#225;rdico es menos frecuente y generalmente asociado con melanoma o linfoma, sugiriendo invasi&#243;n hemat&#243;gena. Linfoma difuso de grandes c&#233;lulas B (LDGCB) es un linfoma no Hodgkin (LNH) con incidencia en individuos infectados por el VIH de m&#225;s de 100 veces la incidencia en la poblaci&#243;n en geral<sup>1</sup>. </p>
      <p>En pacientes con LNH, se&#241;ales cl&#237;nicos de compromiso card&#237;aco son inespec&#237;ficos y frecuentemente no son detectados antes de la muerte. Dolor tor&#225;cico, insuficiencia card&#237;aca congestiva y derrame peric&#225;rdico fueron relatados anteriormente, siendo el &#250;ltimo la presentaci&#243;n m&#225;s com&#250;n<sup>2</sup>. Aunque varios casos de arritmias hayan sido documentados, la mayor&#237;a incluye bloqueo atrioventricular, probablemente relacionado a la lesi&#243;n secundaria del sistema de conducci&#243;n<sup>3</sup>. Arritmias ventriculares son raramente diagnosticadas en esa poblaci&#243;n. Por razones desconocidas, la mayor&#237;a de los casos fue relatada en pacientes con linfoma card&#237;aco prim&#225;rio<sup>4,5</sup>.</p>
      <p>Describimos un caso de compromiso card&#237;aco de LNH, que present&#243; taquicardia ventricular monom&#243;rfica, la cual es una manifestaci&#243;n rara. El diagn&#243;stico fue realizado con base en estudios de imagen obtenidos a trav&#233;s de ecocardiograma transtor&#225;cico, que es un m&#233;todo barato y f&#225;cilmente disponible. Es importante enfatizar que en tales casos, el compromiso card&#237;aco puede ser mejor determinado con modalidades de estudio de imagen m&#225;s sensibles, como la resonancia magn&#233;tica o la tomograf&#237;a computada. Entre tanto, esos m&#233;todos son caros y no siempre est&#225;n disponibles en centros card&#237;acos. El mecanismo asociado con la taquicardia ventricular (TV) podr&#237;a ser secundario al atraso en la conducci&#243;n ventricular causado por invasi&#243;n mioc&#225;rdica localizada de c&#233;lulas del linfoma, aunque la actividad desencadenada no pueda ser excluida. En ese escenario, el estudio electrofisiol&#243;gico puede ser una herramienta valiosa en casos seleccionados para entender los mecanismos de arritmia y la respuesta al tratamiento farmacol&#243;gico. Entre tanto, ning&#250;n estudio prospectivo testando el papel de esa modalidad est&#225; disponible en esa poblaci&#243;n. </p>
      <p>Es posible considerar la hip&#243;tesis de que el reciente tratamiento quimioter&#225;pico caus&#243; la toxicidad mioc&#225;rdica y desencaden&#243; la TV, ya que dos casos de TV fueron anteriormente documentados con el uso de Ifosfamida<sup>6</sup>. Entre tanto, esa hip&#243;tesis es menos favorecida debido a la mejora de los implantes metast&#225;ticos en los d&#237;as subsecuentes con el protocolo ICE. </p>
      <p>En conclusi&#243;n, relatamos un caso poco usual de compromiso card&#237;aco de LNH con TV. La ocurrencia de arritmias en esa poblaci&#243;n siempre debe alertar sobre la posibilidad de compromiso metast&#225;tico en el miocardio.</p>
      <p>
        <bold>Potencial Conflicto de Intereses</bold>
      </p>
      <p>Declaro no haber conflicto de intereses pertinentes.</p>
      <p>
        <bold>Fuentes de Financiaci&#243;n</bold>
      </p>
      <p>El presente estudio no tuve fuentes de financiaci&#243;n externas.</p>
      <p>
        <bold>Vinculaci&#243;n Acad&#233;mica</bold>
      </p>
      <p>Este art&#237;culo forma parte de tesis de Doctorado de Diego Chemello, por <italic>Hospital de Cl&#237;nicas de Porto Alegre - Universidade Federal do Rio Grande do Sul</italic>.</p>
      <p>
        <bold>Referencias</bold>
      </p>
    </body>
  </sub-article>
  <sub-article article-type="translation" id="TRen" xml:lang="en">
    <front-stub>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Case Report</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title xml:lang="en">Ventricular tachycardia associated with non-Hodgkin's lymphoma</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>Systemic non-Hodgkin's lymphoma can affect the myocardium, particularly in immunocompromised patients. When present, symptoms and signs are usually nonspecific, making the diagnosis of cardiac involvement very difficult before an autopsy. Ventricular arrhythmias are also unusual in this setting. We describe a case of secondary myocardial non-Hodgkin's lymphoma presenting with sustained monomorphic ventricular tachycardia and thickening of the basal interventricular septum. Complete remission of myocardial lesions was observed after completion of second-line chemotherapy treatment, without further recurrences of arrhythmias in eight months.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Tachycardia, ventricular</kwd>
        <kwd>heart neoplasms</kwd>
        <kwd>Hodgkin disease</kwd>
        <kwd>linfoma</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>CASE REPORT</bold>
      </p>
      <p>
        <fn id="enda-body3">
          <label>
            <bold>Ventricular tachycardia associated with non-Hodgkin's lymphoma</bold>
          </label>
          <p>
            <bold>Diego Chemello; Priscila Raupp-da-Rosa; Guilherme Tel&#243;; Nadine Clausell</bold>
          </p>
        </fn>
      </p>
      <p>Hospital de Cl&#237;nicas de Porto Alegre - Universidade Federal do Rio Grande do Sul, Porto Alegre, RS - Brasil</p>
      <p>Mailing adress</p>
      <p>
        <bold>ABSTRACT</bold>
      </p>
      <p>Systemic non-Hodgkin's lymphoma can affect the myocardium, particularly in immunocompromised patients. When present, symptoms and signs are usually nonspecific, making the diagnosis of cardiac involvement very difficult before an autopsy. Ventricular arrhythmias are also unusual in this setting. We describe a case of secondary myocardial non-Hodgkin's lymphoma presenting with sustained monomorphic ventricular tachycardia and thickening of the basal interventricular septum. Complete remission of myocardial lesions was observed after completion of second-line chemotherapy treatment, without further recurrences of arrhythmias in eight months.</p>
      <p><bold>Keywords:</bold> Tachycardia, ventricular; heart neoplasms; Hodgkin disease; linfoma/quimioterapia.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>Clinical heart involvement secondary to metastasis of malignant tumors is relatively unusual. Autopsy studies have shown up to 12% of cardiac involvement in all patients with malignancy, and most of them are asymptomatic. Systemic non-Hodgkin's lymphoma is one disease that can affect the myocardium, particularly in immunocompromised patients. The clinical presentation is usually nonspecific. The diagnosis of cardiac involvement can be difficult and requires high clinical suspicion. Ventricular arrhythmias are extremely unusual and only few cases have been described so far. These arrhythmias usually are symptomatic and associated with significant hemodynamic instability. </p>
      <p>
        <bold>Case report</bold>
      </p>
      <p>A 27-year-old female patient presented to the emergency department with sudden-onset palpitations and chest discomfort. Blood pressure was 68 x 40 mmHg and heart rate was 184 bpm. Physical examination also revealed an increased volume in the left breast and a diffuse abdominal mass. The 12-lead electrocardiogram (ECG) performed on the admission revealed a wide-complex tachycardia with left-bundle branch block pattern and negative concordance in precordial leads (<xref ref-type="fig" rid="en_a17fig01-body3">Figure 1A</xref>).</p>
      <p content-type="html"><fig id="en_a17fig01-body3"><graphic xlink:href="https://minio.scielo.br/documentstore/1678-4170/PkqGGwvDQ7rX65xfXWzCRWj/35c48ed06d4ee91c7fc2c4ec13e8d15d3c0b2db4.jpg"/><graphic xlink:href="1678-4170-abc-97-06-e132-00017-gf01-en.jpg"/></fig>&#13;
&#160;&#13;
</p>
      <p>Based on the initial presentation, the diagnosis of monomorphic ventricular tachycardia was established and patient underwent electrical cardioversion to normal sinus rhythm. The ECG was repeated, showing normal sinus rhythm and no ST changes (<xref ref-type="fig" rid="en_a17fig01-body3">Figure 1B</xref>). She was started on intravenous amiodarone infusion and then admitted to the intensive care unit. Investigation was negative for myocardial ischemia or pulmonary embolism. A transthoracic echocardiography (TTE) revealed normal left and right ventricular functions, moderate posterior pericardial effusion and thickening of the basal-septal myocardium, which was not present in previous examination performed one year before for investigation of shortness of breath during physical activities (<xref ref-type="fig" rid="en_a17fig02m-body3">Figure 2A</xref>). Clinical investigation revealed a medical history of acquired immunodeficiency syndrome (AIDS) due to HIV infection in the previous 12 months and initial CD4 count of 39 cells/mm<sup>3</sup>. Immediately after this diagnosis she was started on highly active antiretroviral therapy (HAART), which increased and stabilized CD4 cell counts to 89 cells/mm<sup>3</sup> after three months of treatment. She also received the diagnosis of diffuse large B-cell lymphoma (DLCL), a non-Hodgkin's lymphoma which was initially treated with a combination of Cyclophosphamide, Adriamycin, Vincristine and Prednisone (CHOP). Due to severe neutropenia treatment was changed to Etoposide, Vincristine, Doxorubicin, Cyclophosphamide and Prednisone (EPOCH). Despite a complete course of treatment, lymphoma remission failed (breast and retroperitoneal mass tissue biopsy were positive for DLCL). In the week after the emergency admission, she was started on Ifosfamide, Carboplatin and Etoposide (ICE), a second-line chemotherapy protocol.</p>
      <p content-type="asset">
        <fig id="en_a17fig02m-body3">
          <graphic xlink:href="1678-4170-abc-97-06-e132-00017-gf02-en.jpg"/></fig>
      </p>
      <p>After an Oncology consultation, chemotherapy with ICE regimen for DLCL was continued. Cardiac biopsy was considered, which the patient refused. A new TTE after 30 days of chemotherapy revealed marked improvement, with a decrease in the pericardial effusion, as well as complete reduction in the myocardial septal thickening (<xref ref-type="fig" rid="en_a17fig02m-body3">Figure 2B</xref>). No further arrhythmias were documented in the subsequent eight months. No chronic antiarrhythmic medications were prescribed.</p>
      <p>
        <bold>Discussion</bold>
      </p>
      <p>Metastatic involvement of the heart is discovered at the autopsy in 10 to 12% of patients with malignancies, most frequently of lung carcinoma. The majority of these cases involve the pericardium and epicardium, suggesting a regional lymphatic invasion. Myocardial involvement is less frequent and usually associated with melanoma or lymphoma, suggesting hematogenous invasion. Diffuse large B-cell lymphoma is a NHL with an incidence in HIV-infected individuals over 100 times the incidence in the general population<sup>1</sup>.</p>
      <p>In patients with NHL, clinical signs of cardiac involvement are nonspecific and frequently undetected before death. Chest pain, congestive heart failure and pericardial effusion were previously reported, the latter being the most common presentation<sup>2</sup>. Although several cases of arrhythmias have been documented, most include atrioventricular block, probably related to secondary lesion to the conduction system<sup>3</sup>. Ventricular arrhythmias are rarely diagnosed in this population. For unknown reasons, most cases were reported in patients with primary cardiac lymphoma<sup>4,5</sup>.</p>
      <p>We describe a case of heart involvement in NHL presenting with monomorphic ventricular tachycardia, which is a rare manifestation. The diagnosis was performed based on images obtained from the transthoracic echocardiogram, which is an inexpensive and easily available method. It is important to emphasize that in such cases cardiac involvement can be better determined with more sensitive imaging modalities, such as magnetic resonance or computed tomography. However, these techniques are expensive and not always available in cardiac centers. </p>
      <p>The mechanism associated with ventricular tachycardia could be secondary to ventricular conduction delay caused by localized myocardial invasion of lymphoma cells, although triggered activity cannot be excluded. In this setting, the electrophysiological study can be a valuable tool in selected cases to understand the arrhythmia mechanisms and response to pharmacological treatment. However, no prospective studies testing the role of this modality are available in such population.</p>
      <p>One could hypothesize that the recent chemotherapy treatment caused myocardial toxicity and triggered VT, since two cases of ventricular arrhythmias were previously documents with Ifosfamide use<sup>6</sup>. However, this hypothesis is less favored due to the improvement in the metastatic implants in the following days with the ICE protocol.</p>
      <p>In conclusion, we report an unusual case of cardiac involvement of NHL presenting with VT. The occurrence of arrhythmias in this population should always alert for the possibility of metastatic involvement of the myocardium.</p>
      <p>
        <bold>Potential Conflict of Interest</bold>
      </p>
      <p>No potential conflict of interest relevant to this article was reported.</p>
      <p>
        <bold>Sources of Funding</bold>
      </p>
      <p>There were no external funding sources for this study.</p>
      <p>
        <bold>Study Association</bold>
      </p>
      <p>This article is part of the thesis of doctoral submitted by Diego Chemello , from <italic>Hospital de Cl&#237;nicas de Porto Alegre - Universidade Federal do Rio Grande do Sul</italic>.</p>
      <p>
        <bold>References</bold>
      </p>
    </body>
  </sub-article>
</article>
