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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">Y54knBrLsycTHnXJJq77zmg</article-id>
      <article-id pub-id-type="other">00011</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2007001400011</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(07)08900211</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2007001400011</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Correla&#231;&#227;o Cl&#237;nico-Radiogr&#225;fica</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Caso 4/2007: lactente de 16 meses com canal arterial</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Atik</surname>
            <given-names>Edmar</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="city">S&#227;o Paulo</named-content>
          <named-content content-type="state">SP</named-content>
        </addr-line>
        <institution content-type="orgname">FMUSP</institution>
        <institution content-type="orgdiv1">Hospital das Cl&#237;nicas </institution>
        <institution content-type="orgdiv2">Instituto do Cora&#231;&#227;o</institution>
        <country country="BR">Brasil</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>08</month>
        <year>2007</year>
      </pub-date>
      <volume>89</volume>
      <issue>2</issue>
      <fpage>135</fpage>
      <lpage>136</lpage>
      <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>
      <pub-date publication-format="electronic" date-type="pub">
        <day>05</day>
        <month>09</month>
        <year>2007</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>
      <bold>CORRELA&#199;&#195;O CL&#205;NICO-RADIOGR&#193;FICA</bold>
    </p>
    <p>Caso 4/2007 &#150; Lactente de 16 meses com canal arterial</p>
    <p>
      <bold>Edmar Atik</bold>
    </p>
    <p> Instituto do Cora&#231;&#227;o do Hospital das Cl&#237;nicas &#150; FMUSP &#150; S&#227;o Paulo, SP - Brasil</p>
    <p>
      <xref ref-type="corresp" rid="end">Correspond&#234;ncia</xref>
    </p>
    <p><bold>Palavras-chave:</bold> lactente, persist&#234;ncia do tronco arterial, cardiopatias cong&#234;nitas.</p>
    <p>
      <bold>Dados cl&#237;nicos</bold>
    </p>
    <p>Lactente de 16 meses de idade, do sexo feminino e de cor branca, apresentava cansa&#231;o &#224;s mamadas desde 30 dias de vida, de car&#225;ter progressivo. No primeiro ano houve epis&#243;dios repetidos de infec&#231;&#245;es de vias a&#233;reas superiores e h&#225; dois meses, broncopneumonia. Defeito card&#237;aco foi diagnosticado por ecocardiografia aos 11 meses de idade, tendo sido institu&#237;da, desde ent&#227;o, medica&#231;&#227;o anticongestiva. Ao exame f&#237;sico estava em bom estado geral, com taquipn&#233;ia discreta, acian&#243;tica e com pulsos amplos nos quatro membros. O peso era de 9.860 g; a altura, 76,5 cm; a satura&#231;&#227;o de oxig&#234;nio, 96%; a freq&#252;&#234;ncia card&#237;aca, 125 bpm; e a press&#227;o arterial, 100/50 mmHg. A aorta n&#227;o foi palpada. No prec&#243;rdio, havia impuls&#245;es discretas na borda esternal esquerda e o <italic>ictus cordis</italic> era localizado no 4&#186; espa&#231;o intercostal esquerdo, muscular, +/++, limitado por duas polpas digitais. As bulhas eram hiperfon&#233;ticas, sendo &#250;nica a 2&#170; bulha. Havia sopro cont&#237;nuo, ++, suave, no 2&#186;, no 3&#186; e no 1&#186; espa&#231;os intercostais esquerdos, com irradia&#231;&#227;o &#224; &#225;rea tric&#250;spide. O f&#237;gado foi palpado a 2 cm do rebordo costal direito.</p>
    <p>O eletrocardiograma demonstrou ritmo sinusal e sinais de sobrecarga ventricular esquerda, com ondas R amplas em V4 e V5, com &#237;ndice de Sokollof de 50 mm. S&#194;P: +60&#186;, S&#194;QRS: +20&#186;, S&#194;T: +60&#186;.</p>
    <p>
      <bold>Imagem radiogr&#225;fica</bold>
    </p>
    <p>Imagem demonstrando &#225;rea card&#237;aca aumentada, &#224; custa do arco ventricular esquerdo, acentuadamente desviado. O arco m&#233;dio &#233; retificado e a traqu&#233;ia &#233; desviada para a direita, em decorr&#234;ncia do aumento da aorta com arco a&#243;rtico &#224; esquerda e com trama vascular pulmonar nitidamente aumentada (<xref ref-type="fig" rid="fig01">fig. 1</xref>).</p>
    <fig id="fig01">
      <graphic xlink:href="1678-4170-abc-89-02-0135-00011-gf01.jpg"/></fig>
    <p>
      <bold>Impress&#227;o diagn&#243;stica</bold>
    </p>
    <p>Essa imagem sugere aumento do fluxo pulmonar por <italic>shunt</italic> de sangue a n&#237;vel arterial, pela persist&#234;ncia do canal arterial, decorrente do aumento de ambas as art&#233;rias e do ventr&#237;culo esquerdo. </p>
    <p>
      <bold>Diagn&#243;stico diferencial</bold>
    </p>
    <p>Cardiopatias afins ao canal arterial, como f&#237;stulas arteriovenosas e janela aortopulmonar, devem ser distinguidas.</p>
    <p>
      <bold>Confirma&#231;&#227;o diagn&#243;stica</bold>
    </p>
    <p>Os elementos cl&#237;nicos sugerem diagn&#243;stico de canal arterial, em decorr&#234;ncia da posi&#231;&#227;o alta na borda esternal esquerda do sopro cont&#237;nuo, raramente encontrada em outros tipos de comunica&#231;&#227;o sist&#234;mico-pulmonar. O ecocardiograma (<xref ref-type="fig" rid="fig02">fig. 2</xref>) demonstrou dilata&#231;&#227;o moderada das cavidades esquerdas, com canal arterial de 8 mm de di&#226;metro e grande fluxo cont&#237;nuo da esquerda para a direita. As medidas encontradas foram: ventr&#237;culo direito, 10 mm; di&#226;metro diast&#243;lico de ventr&#237;culo esquerdo, 39 mm; aorta, 15 mm; e septo e parede, 5 mm.</p>
    <fig id="fig02">
      <graphic xlink:href="1678-4170-abc-89-02-0135-00011-gf02.jpg"/></fig>
    <p>
      <bold>Conduta</bold>
    </p>
    <p>&#192; opera&#231;&#227;o, o canal arterial de 3 mm de di&#226;metro foi seccionado e suturado. A evolu&#231;&#227;o foi boa, com desaparecimento total do sopro card&#237;aco.</p>
    <p>
      <fn id="end" fn-type="corresp">
        <label>
          <bold>Correspond&#234;ncia:</bold>
        </label>
        <p> Edmar Atik </p>
        <p> InCor </p>
        <p> Av. Dr. En&#233;as de Carvalho Aguiar, 44 </p>
        <p> 05403-000 - S&#227;o Paulo, SP - Brasil </p>
        <p> E-mail: </p>
        <p>
          <email xlink:href="conatik@incor.usp.br">conatik@incor.usp.br</email>
        </p>
      </fn>
    </p>
  </body>
  <sub-article article-type="translation" id="TRen" xml:lang="en">
    <front-stub>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Clinicalradiological Session</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title xml:lang="en">Case 4/2007: a sixteen-month-old infant with patent ductus arteriosus</article-title>
      </title-group>
    </front-stub>
    <body>
      <p>
        <bold>CLINICORADIOLOGIAL SESSION</bold>
      </p>
      <p>Case 4/2007 &#150; A sixteen-month-old infant with patent <italic><bold>ductus arteriosus</bold></italic></p>
      <p>
        <bold>Edmar Atik</bold>
      </p>
      <p> Instituto do Cora&#231;&#227;o do Hospital das Cl&#237;nicas - FMUSP - S&#227;o Paulo, SP - Brazil</p>
      <p>
        <xref ref-type="corresp" rid="end-body2">Mailing address</xref>
      </p>
      <p><bold>Key words:</bold> Infant; <italic>truncus arteriosus</italic>, persistent; heart defects, congenital.</p>
      <p>
        <bold>Clinical data</bold>
      </p>
      <p>A sixteen-month-old white female infant with history of fatigue during feeding since she was 30 days old, which was progressive in nature. In the first year, she experienced recurrent upper respiratory tract infections, and two months ago had bronchopneumonia. At the age of eleven months, she was diagnosed with a heart defect, and since then had been taking anticongestive medication. On physical examination she was in good general condition, with mild tachypnea and wide pulse pressure in the upper and lower extremities. No cyanosis was observed. She weighed 9,860 g and was 76.5 cm tall. Oxygen saturation was 96%, heart rate was 125 bpm and blood pressure was 100/50 mm Hg. The aorta was not palpable. Chest examination showed mild impulses along the left sternal border, and a muscular apical impulse +/++ was located at the fourth left intercostal space limited by the breadth of two fingers. Heart sounds were very loud, and the second sound was single. A continuous, ++, mild murmur was heard at the 2<sup>nd</sup>, 3<sup>rd</sup>, and 1<sup>st</sup> left intercostal space that radiated to the tricuspid area. The liver was palpable 2 cm from the right costal margin.</p>
      <p>The electrocardiogram showed sinus rhythm and signs of left ventricular volume overload, with tall R waves in leads V4 and V5 and a Sokollof index of 50 mm.</p>
      <p>P-axis:+60&#186;, QRS-axis:+20&#186;, T-axis:+60&#186;.</p>
      <p>
        <bold>Radiographic examination</bold>
      </p>
      <p>Radiographic findings included an enlarged cardiac silhouette due to a markedly displaced left ventricular arch; a straight mid-arch; and a rightward deviation of the trachea, considering the aorta enlargement with the aortic arch to the left and clearly increased pulmonary vascularity. (<xref ref-type="fig" rid="fig01-body2">Fig. 1</xref>).</p>
      <fig id="fig01-body2">
        <graphic xlink:href="1678-4170-abc-89-02-0135-00011-gf01-en.jpg"/></fig>
      <p>
        <bold>Diagnostic impression</bold>
      </p>
      <p>This image suggests an increase in pulmonary shunt flow secondary to patent <italic>ductus arteriosus</italic>, as shown by the enlargement of both arteries and the left ventricle.</p>
      <p>
        <bold>Differential diagnosis</bold>
      </p>
      <p><italic>Ductus arteriosus</italic>-related heart diseases, such as arteriovenous fistula and aortopulmonary window, must be recognized.</p>
      <p>
        <bold>Diagnostic confirmation</bold>
      </p>
      <p>Clinical findings are consistent with <italic>ductus arteriosus</italic>, based on the continuous murmur heard at the high left sternal border and rarely found in other types of systemic-to-pulmonary communication. The echocardiogram (<xref ref-type="fig" rid="fig02-body2">Fig. 2</xref>) showed moderately dilated left chambers with an 8-mm patent <italic>ductus arteriosus</italic> and a large, continuous, left-to-right flow. The following measurements were found: right ventricle 10 mm, left ventricular diastolic diameter 39 mm, aorta 15 mm, and septal and wall thickness 5 mm.</p>
      <fig id="fig02-body2">
        <graphic xlink:href="1678-4170-abc-89-02-0135-00011-gf02-en.jpg"/></fig>
      <p>
        <bold>Management</bold>
      </p>
      <p>During surgery, the 3-mm <italic>ductus arteriosus</italic> was sectioned and sutured. The baby girl evolved favorably, and the heart murmur disappeared completely.</p>
      <p>
        <fn id="end-body2" fn-type="corresp">
          <p>Mailing address:</p>
          <p> Edmar Atik</p>
          <p> InCor</p>
          <p> Av. Dr En&#233;as de Carvalho Aguiar, 44</p>
          <p> 05403-000 - S&#227;o Paulo, SP - Brazil </p>
          <p> E-mail: </p>
          <p>
            <email xlink:href="conatik@incor.usp.br">conatik@incor.usp.br</email>
          </p>
        </fn>
      </p>
    </body>
  </sub-article>
</article>
