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<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" article-type="case-report" dtd-version="1.0" specific-use="sps-1.3" xml:lang="en">
  <front>
    <journal-meta>
      <journal-id journal-id-type="nlm-ta">Arq Bras Cardiol</journal-id>
      <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>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v3">sVQL3xTLpq7bYxN7grKW7mv</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2016000200153</article-id>
      <article-id pub-id-type="doi">10.5935/abc.20160023</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Clinicoradiological Session</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Case 2/2016 - Scimitar Sign with Right Pulmonary Vein Drainage into the Right Atrium</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="aff1"/>
          <xref ref-type="corresp" rid="c1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Arrieta</surname>
            <given-names>Raul</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Kalil</surname>
            <given-names>Roberto</given-names>
            <suffix>Filho</suffix>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <aff id="aff1">
          <institution content-type="orgname">Hospital S&#237;rio Liban&#234;s</institution>
          <addr-line>
            <named-content content-type="city">S&#227;o Paulo</named-content>
            <named-content content-type="state">SP</named-content>
          </addr-line>
          <country country="BR">Brazil</country>
          <institution content-type="original">Hospital S&#237;rio Liban&#234;s, S&#227;o Paulo, SP - Brazil</institution>
          <institution content-type="normalized">Hospital S&#237;rio-Liban&#234;s</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="c1"><bold>Mailing Address: Edmar Atik</bold>, Office. Rua Dona Adma Jafet, 74, conj.73, Bela Vista. Postal Code 01308-050, S&#227;o Paulo, SP - Brasil. E-mail: <email>edmaratik@uol.com.br</email>
					</corresp>
      </author-notes>
      <pub-date pub-type="epub-ppub">
        <month>02</month>
        <year>2016</year>
      </pub-date>
      <volume>106</volume>
      <issue>2</issue>
      <fpage>153</fpage>
      <lpage>155</lpage>
      <history>
        <date date-type="received">
          <day>14</day>
          <month>07</month>
          <year>2015</year>
        </date>
        <date date-type="rev-recd">
          <day>16</day>
          <month>09</month>
          <year>2015</year>
        </date>
        <date date-type="accepted">
          <day>16</day>
          <month>09</month>
          <year>2015</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0">
          <license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
        </license>
      </permissions>
      <kwd-group xml:lang="en">
        <title>Keywords</title>
        <kwd>Scimitar Syndrome / surgery</kwd>
        <kwd>Pulmonary Veins / abnormalities</kwd>
        <kwd>Radiography, Thoracic</kwd>
        <kwd>Cardiac Catheterization</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <p><bold>Clinical data:</bold> the characteristic signs of the scimitar syndrome with right pulmonary hypoplasia were discovered in an asymptomatic patient through routine chest X-ray, in the presence of dengue.</p>
    <p>On physical examination, the patient was in good general health status, eupneic, normal skin color, with normal pulses. His weight was 54 kg, height 155 cm, blood pressure of 100/60 mmHg, heart rate of 88 bpm.</p>
    <p>The aorta was not palpable at the sternal notch. In the precordium, there were mild impulses at the left and right sternal borders and the apex beat was not palpable. Heart sounds were normal, with constant splitting of the second heart sound, with discreet and rough ejection systolic murmur in the pulmonary area.</p>
    <p>The liver was not palpable and in the lungs, breath sounds were less audible in the right lower pulmonary lobe.</p>
    <sec>
      <title>Complementary tests</title>
      <p><bold>The Electrocardiogram</bold> showed sinus rhythm and signs of final conduction disturbance in the right branch with rSr' complex in V1. There were no signs of cavity overload. AP: +70, AQRS: + 80&#186;, AT: + 10 (<xref ref-type="fig" rid="f1">Figure 1</xref>).</p>
      <p>
        <fig id="f1">
          <label>Figure 1</label>
          <caption>
            <title>Chest X-ray showed heart dextroposition due to right lung hypoplasia and the scimitar sign (arrows) of the dilated and anomalous right pulmonary vein. Electrocardiogram showed the classic signs of right ventricular volume overload with rSR' complex in V1.</title>
          </caption>
          <graphic xlink:href="1678-4170-abc-106-02-0153-60023-gf01.jpg"/></fig>
      </p>
      <p><bold>The Chest X-ray</bold> disclosed right lung hypoplasia, dextroposition of the heart as a result of it and the classic sign of anomalous pulmonary vein drainage to the right, with scimitar aspect. The pulmonary vasculature to the left was slightly more prominent (<xref ref-type="fig" rid="f1">Figure 1</xref>).</p>
      <p><bold>The Echocardiogram</bold> showed enlargement of the right heart chambers, pulmonary arteries and right pulmonary vein drainage into the right atrium at its lower portion, near the inferior vena cava.</p>
      <p><bold>The CT angiography</bold> disclosed the same aspect, in addition to the obvious systemic-pulmonary collateral circulation from the descending aorta into the right lower pulmonary lobe (<xref ref-type="fig" rid="f2">Figure 2</xref>).</p>
      <p>
        <fig id="f2">
          <label>Figure 2</label>
          <caption>
            <title>CT angiography in A showing the right pulmonary vein (RPV, arrow) draining into the right atrium (RA); angiography shows the scimitar sign (arrows) of the RPV in B and draining into the RA in C; systemic-pulmonary collateral vessel emerging from the descending aorta into the right lower lobe (pulmonary sequestration) in D and after its embolization in E.</title>
          </caption>
          <graphic xlink:href="1678-4170-abc-106-02-0153-60023-gf02.jpg"/></fig>
      </p>
      <p><bold>Diagnosis:</bold> Scimitar syndrome with right pulmonary vein drainage into the right atrium with moderate repercussion and pulmonary sequestration in systemic-pulmonary circulation of the descending aorta into the right lower lobe.</p>
      <p><bold>Clinical reasoning:</bold> the scimitar syndrome, due to the anomalous right pulmonary vein drainage, is clinically manifested as a simple atrial septal defect, with the described classic signs, few symptoms, ejection murmur in the pulmonary area, splitting of the second heart sound and right ventricular diastolic overload on the electrocardiogram. The scimitar sign on the chest X-ray easily characterizes the diagnosis of the syndrome, as this diagnosis had been established in this case. Hence, the importance of this complementary radiographic assessment, simple and definitive, to achieve a diagnostic conclusion of this defect.</p>
      <p><bold>Differential diagnosis:</bold> the scimitar syndrome shows no diagnostic difficulties in comparison to other defects, as it has a characteristic and unique radiographic sign.</p>
      <p><bold>Conduct:</bold> the diagnostic confirmation by cardiac catheterization was scheduled, in addition to the embolization of the systemic-pulmonary vessel, and subsequently, the surgical repair of the anomalous right pulmonary vein drainage was performed. The hemodynamic study showed normal pressures in the heart chambers and arteries (RA = 8, RV = 25/8, PT = 25 / 15-20, Ao = 98 / 58-70 mmHg). Arterial saturation was 100% in the aorta. The angiography showed a large pulmonary venous vessel to the right, quite dilated, which drained into the low right atrium. The injection of contrast into the descending aorta showed an arterial vessel going into the right lower lobe after mild stenosis in its proximal third. It was totally occluded after the placement of three coils (<xref ref-type="fig" rid="f2">Figure 2</xref>).</p>
      <p>At the cardiac surgery, after starting the cardiopulmonary bypass, the interatrial septum was partially resected and the right pulmonary vein flow was redirected into the left atrium using a bovine pericardium patch.</p>
      <p>The postoperative course was uneventful, with disappearance of the heart murmur.</p>
      <p><bold>Comments:</bold> In classic scimitar syndrome, it is known that drainage of the anomalous pulmonary veins of the right lung in the shape of a scimitar (curved Turkish sword) is directed into the inferior vena cava, with a higher or lower degree of right lung hypoplasia, with or without pulmonary sequestration by the systemic-pulmonary vessel of the aorta to the right lower lobe, as well as dextroposition of the heart. <xref ref-type="bibr" rid="B1">1</xref><sup>,</sup><xref ref-type="bibr" rid="B2">2</xref> Most cases are not associated with other defects (75%) and this syndrome shows two different types: the one identified in children (with dynamic repercussions) and the adult type (with less impact of volume overload, related to the degree of right pulmonary hypoplasia). However, the drainage into the right atrium of the right pulmonary veins, while maintaining the scimitar shape is little known. After searching the literature since 1966, we did not find any similar cases to the one described here, with drainage of the anomalous vein directly into the right atrium and the classic scimitar sign. This peculiarity of the scimitar shape persists due to the proximity of the drainage in the lower right atrium, near the inferior vena cava. In this context, there have been reported cases of the scimitar sign, but with normal drainage of the right pulmonary vein into the left atrium itself.<xref ref-type="bibr" rid="B3">3</xref> Thus, we currently know the "characteristic scimitar syndrome" and the "scimitar sign" - the latter not associated with the anomalous pulmonary vein drainage or associated with anomalous drainage at another site, such as in the right atrium, for instance.</p>
    </sec>
  </body>
  <back>
    <ref-list>
      <title>References</title>
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          <article-title>Eponym. Scimitar syndrome</article-title>
          <source>Eur J Pediatr</source>
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        <mixed-citation>3 Holt PD, Berdon WE, Marans Z, Griffiths S, Hsu D. Scimitar vein draining to the left atrium and a historical review of the scimitar syndrome. Pediatr Radiol. 2004;34(5):409-13.</mixed-citation>
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  </back>
  <sub-article article-type="translation" id="s1" xml:lang="pt">
    <front-stub>
      <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 2/2016 - Sinal de Cimitarra em Drenagem de Veias Pulmonares Direitas no &#193;trio Direito</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="aff2"/>
          <xref ref-type="corresp" rid="c2"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Arrieta</surname>
            <given-names>Raul</given-names>
          </name>
          <xref ref-type="aff" rid="aff2"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Kalil</surname>
            <given-names>Roberto</given-names>
            <suffix>Filho</suffix>
          </name>
          <xref ref-type="aff" rid="aff2"/>
        </contrib>
        <aff id="aff2">
          <institution content-type="orgname">Hospital S&#237;rio Liban&#234;s</institution>
          <addr-line>
            <named-content content-type="city">S&#227;o Paulo</named-content>
            <named-content content-type="state">SP</named-content>
          </addr-line>
          <country country="BR">Brasil</country>
          <institution content-type="original">Hospital S&#237;rio Liban&#234;s, S&#227;o Paulo, SP - Brasil</institution>
          <institution content-type="normalized">Hospital S&#237;rio-Liban&#234;s</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="c2"><bold>Correspond&#234;ncia: Edmar Atik</bold>, Consult&#243;rio privado. Rua Dona Adma Jafet, 74, conj.73, Bela Vista. CEP: 01308-050, S&#227;o Paulo, SP - Brasil. E-mail: <email>edmaratik@uol.com.br</email>
					</corresp>
      </author-notes>
      <kwd-group xml:lang="pt">
        <title>Palavras-chave</title>
        <kwd>S&#237;ndrome de Cimitarra / cirurgia</kwd>
        <kwd>Veias Pulmonares / anormalidades</kwd>
        <kwd>Radiografia Tor&#225;cica</kwd>
        <kwd>Cateterismo Card&#237;aco</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p><bold>Dados cl&#237;nicos:</bold> descoberto de rotina por radiografia de t&#243;rax os sinais caracter&#237;sticos da s&#237;ndrome da cimitarra com hipoplasia pulmonar direita, em vig&#234;ncia de dengue, em paciente assintom&#225;tico.</p>
      <p>No exame f&#237;sico, estava em bom estado geral, eupn&#233;ico, corado, com pulsos normais. Peso de 54 kg, altura de 155 cm, press&#227;o arterial de 100/60 mmHg, frequ&#234;ncia card&#237;aca de 88 bpm.</p>
      <p>Aorta n&#227;o era palpada na f&#250;rcula. No prec&#243;rdio, havia impuls&#245;es discretas na borda esternal direita e esquerda, e o <italic>ictus</italic> n&#227;o era palpado. As bulhas eram normofon&#233;ticas, e a segunda bulha, desdobrada constante com sopro sist&#243;lico de eje&#231;&#227;o, discreto e rude, na &#225;rea pulmonar.</p>
      <p>O f&#237;gado n&#227;o era palpado e, nos pulm&#245;es, o murm&#250;rio vesicular era menos aud&#237;vel no ter&#231;o pulmonar inferior direito.</p>
      <sec>
        <title>Exames complementares</title>
        <p><bold>Eletrocardiograma</bold> salientava ritmo sinusal e sinais de dist&#250;rbio final de condu&#231;&#227;o pelo ramo direito com complexo rSr' em V1. N&#227;o havia sinais de sobrecarga cavit&#225;ria. AP: +70&#186;, AQRS: +80&#186;, AT: +10&#186; (<xref ref-type="fig" rid="f3">Figura 1</xref>).</p>
        <p>
          <fig id="f3">
            <label>Figura 1</label>
            <caption>
              <title>Radiografia de t&#243;rax mostra cora&#231;&#227;o dextroposto por hipoplasia do pulm&#227;o direito e o sinal de cimitarra (setas) da veia pulmonar direita dilatada e an&#244;mala. Eletrocardiograma com os sinais cl&#225;ssicos da sobrecarga de volume do ventr&#237;culo direito com complexo rSR'em V1.</title>
            </caption>
            <graphic xlink:href="1678-4170-abc-106-02-0153-60023-gf01-pt.jpg"/></fig>
        </p>
        <p><bold>Radiografia de t&#243;rax</bold> mostra a hipoplasia do pulm&#227;o direito, o cora&#231;&#227;o dextroposto em decorr&#234;ncia e o sinal cl&#225;ssico da drenagem an&#244;mala de veias pulmonares &#224; direita, com aspecto de cimitarra. A trama vascular pulmonar &#224; esquerda era ligeiramente mais proeminente (<xref ref-type="fig" rid="f3">Figura 1</xref>)</p>
        <p><bold>Ecocardiograma</bold> mostrava aumento das cavidades card&#237;acas direitas, das art&#233;rias pulmonares e drenagem da veia pulmonar direita no &#225;trio direito em sua por&#231;&#227;o inferior, pr&#243;ximo &#224; veia cava inferior.</p>
        <p><bold>Angiotomografia</bold> salientou o mesmo aspecto, al&#233;m da evidente circula&#231;&#227;o colateral sist&#234;mico-pulmonar, partindo da aorta descendente em dire&#231;&#227;o ao lobo pulmonar inferior direito (<xref ref-type="fig" rid="f4">Figura 2</xref>).</p>
        <p>
          <fig id="f4">
            <label>Figura 2</label>
            <caption>
              <title>Angiotomografia em A mostra a veia pulmonar direita (VPD, seta) drenando no &#225;trio direito (AD); angiografia salienta o sinal da cimitarra (setas) da VPD em B e drenando no AD em C; vaso colateral sist&#234;mico-pulmonar emerge da aorta descendente em dire&#231;&#227;o ao lobo inferior direito (sequestro pulmonar) em D e ap&#243;s emboliza&#231;&#227;o do mesmo em E.</title>
            </caption>
            <graphic xlink:href="1678-4170-abc-106-02-0153-60023-gf02-pt.jpg"/></fig>
        </p>
        <p><bold>Diagn&#243;stico:</bold> s&#237;ndrome da cimitarra com drenagem de veias pulmonares direitas no &#225;trio direito com repercuss&#227;o moderada e sequestro pulmonar em circula&#231;&#227;o sist&#234;mico-pulmonar da aorta descendente em lobo inferior direito.</p>
        <p><bold>Racioc&#237;nio cl&#237;nico:</bold> a s&#237;ndrome da cimitarra, em decorr&#234;ncia da drenagem an&#244;mala das veias pulmonares direitas, expressa-se clinicamente como se fosse uma comunica&#231;&#227;o interatrial simples, com os sinais cl&#225;ssicos descritos, com poucos sintomas, sopro de eje&#231;&#227;o na &#225;rea pulmonar, segunda bulha desdobrada e sobrecarga diast&#243;lica de ventr&#237;culo direito no eletrocardiograma. O sinal da cimitarra, na radiografia de t&#243;rax, caracteriza facilmente o diagn&#243;stico da s&#237;ndrome, como ali&#225;s esse diagn&#243;stico havia sido estabelecido no caso presente. Da&#237; a import&#226;ncia desse exame radiogr&#225;fico complementar, simples e definitivo, para a conclus&#227;o diagn&#243;stica deste defeito.</p>
        <p><bold>Diagn&#243;stico diferencial:</bold> a s&#237;ndrome de cimitarra n&#227;o encontra dificuldades diagn&#243;sticas em rela&#231;&#227;o a outros defeitos, por ser um sinal radiogr&#225;fico caracter&#237;stico e singular.</p>
        <p><bold>Conduta:</bold> programada a confirma&#231;&#227;o diagn&#243;stica por cateterismo card&#237;aco, al&#233;m da interven&#231;&#227;o de emboliza&#231;&#227;o do vaso sist&#234;mico-pulmonar para, em seguida, realizar-se a corre&#231;&#227;o cir&#250;rgica da drenagem an&#244;mala das veias pulmonares direitas. O estudo hemodin&#226;mico revelou press&#245;es normais nas cavidades card&#237;acas e vasos arteriais (AD = 8, VD = 25/8, TP = 25/15-20, Ao = 98/58-70 mmHg). A satura&#231;&#227;o arterial era de 100% na aorta. A angiografia revelou grande vaso venoso pulmonar &#224; direita, bastante dilatado, que drenava no &#225;trio direito baixo. Inje&#231;&#227;o de contraste na aorta descendente evidenciou um vaso arterial, que se dirigia para o lobo inferior direito ap&#243;s discreta estenose no ter&#231;o proximal. A coloca&#231;&#227;o de tr&#234;s molas o ocluiu totalmente (<xref ref-type="fig" rid="f4">Figura 2</xref>).</p>
        <p>Na cirurgia card&#237;aca, ap&#243;s entrada em circula&#231;&#227;o extracorp&#243;rea, foi ressecado parcialmente o septo interatrial e feito o redirecionamento do fluxo da veia pulmonar direita para o &#225;trio esquerdo com remendo de peric&#225;rdio bovino.</p>
        <p>A evolu&#231;&#227;o p&#243;s-operat&#243;ria transcorreu sem intercorr&#234;ncias, com desaparecimento do sopro card&#237;aco.</p>
        <p><bold>Coment&#225;rios:</bold> na s&#237;ndrome da cimitarra cl&#225;ssica, sabe-se que a drenagem das veias pulmonares an&#244;malas do pulm&#227;o direito em forma de cimitarra (espada curva turca) se dirige para a veia cava inferior, em maior ou menor grau de hipoplasia do pulm&#227;o direito, com ou sem sequestro pulmonar por vaso sist&#234;mico-pulmonar da aorta ao lobo inferior direito, al&#233;m da dextroposi&#231;&#227;o card&#237;aca.<xref ref-type="bibr" rid="B1">1</xref><sup>,</sup><xref ref-type="bibr" rid="B2">2</xref> A maioria n&#227;o &#233; associada a outros defeitos (75%) e se distinguem nessa s&#237;ndrome dois tipos, o infantil (com repercuss&#227;o din&#226;mica) e o adulto (de menor repercuss&#227;o da sobrecarga de volume, relacionada ao grau da hipoplasia pulmonar direita). No entanto, a drenagem em &#225;trio direito das veias pulmonares direitas com manuten&#231;&#227;o da forma de cimitarra &#233; pouco conhecida. Na procura da literatura, ali&#225;s, desde 1966, n&#227;o foi encontrado nenhum caso semelhante a este descrito, com drenagem da veia an&#244;mala diretamente no &#225;trio direito e com sinal cl&#225;ssico de cimitarra. Essa particularidade da forma de cimitarra persiste pela proximidade da drenagem no &#225;trio direito inferior, pr&#243;ximo da veia cava inferior. Nesse contexto, h&#225; casos descritos do sinal de cimitarra mas com drenagem normal da veia pulmonar direita no pr&#243;prio &#225;trio esquerdo.<xref ref-type="bibr" rid="B3">3</xref> Da&#237; que conhece-se hoje a "s&#237;ndrome caracter&#237;stica de cimitarra" e o "sinal de cimitarra" - este n&#227;o associado &#224; drenagem an&#244;mala de veia pulmonar ou ainda associado &#224; drenagem an&#244;mala em outro s&#237;tio, como no &#225;trio direito, por exemplo.</p>
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