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<article article-type="abstract" dtd-version="1.0" xml:lang="en" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML">
<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">CC</journal-id>
<journal-id journal-id-type="nlm-ta">Cardiol Croat</journal-id>
<journal-title-group>
<journal-title>Cardiologia Croatica</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Cardiol. Croat.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="ppub">1848-543X</issn>
<issn pub-type="epub">1848-5448</issn>
<publisher><publisher-name>Croatian Cardiac Society</publisher-name></publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">CC 2022 17_9-10_226-7</article-id>
<article-id pub-id-type="doi">10.15836/ccar2022.226</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Extended Abstract</subject></subj-group>
<subj-group subj-group-type="subheading"><subject>Echocardiography, MSCT, MRI</subject></subj-group>
</article-categories>
<title-group>
<article-title>Coronary sinus septal defect (unroofed coronary sinus): a case report</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0608-3962</contrib-id><name><surname>Bili&#x0107;-Pavlinovi&#x0107;</surname><given-names>Matea</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1">*</xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8359-637X</contrib-id><name><surname>Rumora</surname><given-names>Tony</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6674-6735</contrib-id><name><surname>Bakovi&#x0107;</surname><given-names>Drago</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3490-5505</contrib-id><name><surname>Do&#x0161;en</surname><given-names>Denis</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6910-9720</contrib-id><name><surname>Vrane&#x0161;i&#x0107;</surname><given-names>Irena Ivanac</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7378-944X</contrib-id><name><surname>Ani&#x0107;</surname><given-names>Darko</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4004-7271</contrib-id><name><surname>Mari&#x0107;-Be&#x0161;i&#x0107;</surname><given-names>Kristina</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib>
<aff id="aff1"><label>1</label><institution>University of Zagreb</institution>, <institution content-type="dept">School of Medicine</institution>, <addr-line>Zagreb</addr-line>, <country country="hr">Croatia</country></aff>
<aff id="aff2"><label>2</label><institution>University Hospital Centre Zagreb</institution>, <addr-line>Zagreb</addr-line>, <country country="hr">Croatia</country></aff>
</contrib-group>
<author-notes>
<corresp id="cor1"><label>*</label>ADDRESS FOR CORRESPONDENCE: Matea Bili&#x0107;-Pavlinovi&#x0107;, Medicinski Fakultet Sveu&#x010D;ili&#x0161;ta u Zagrebu, &#x0160;alata 3, HR-10000 Zagreb, Croatia. / Phone: +385-91-448-8722 / E-mail: <email xlink:href="bilicka161@gmail.com">bilicka161@gmail.com</email></corresp></author-notes>
<pub-date pub-type="epub-ppub"><month>11</month><year>2022</year></pub-date>
<volume>17</volume>
<issue>9-10</issue>
<fpage>226</fpage>
<lpage>227</lpage>
<history>
<date date-type="received"><day>03</day><month>11</month><year>2022</year></date>
<date date-type="accepted"><day>10</day><month>11</month><year>2022</year></date>
</history>
<permissions>
<copyright-year>2022</copyright-year>
<copyright-holder>Croatian Cardiac Society</copyright-holder>
</permissions>
<kwd-group kwd-group-type="author"><title>KEYWORDS: </title><kwd>pulmonary hypertension</kwd><kwd>coronary sinus septal defect</kwd><kwd>unroofed coronary sinus</kwd><kwd>echocardiography</kwd></kwd-group>
</article-meta>
</front>
<body>
<p><bold>Introduction</bold>: Coronary sinus (CS) atrial septal defect (ASD) is a congenital abnormality of both the atrial septum and the CS that falls within a wide spectrum of unroofed coronary sinus syndrome (URCS) (<xref ref-type="bibr" rid="r1"><italic>1</italic></xref>). The rarest type of ASD called &#x2018;isolated CS ASD&#x2019; can be found in less than 1% of all ASDs. This case report aims to highlight the symptoms and diagnostic approach in an elderly patient with CS ASD.</p>
<p><bold>Case report:</bold> We present a 60-year-old man who complained of moderate effort dyspnea lasting more than 12 months. He was treated for arterial hypertension, atrial fibrillation and had a history of pulmonary hypertension of unknown etiology. Physical examination showed an accentuated second heart sound over the pulmonary ostium with a systolic murmur. Transthoracic echocardiography showed pulmonary hypertension, right ventricular hypertrophy and dilatation, enlargement of both atria, a dilated coronary sinus and no visible atrial septal defects. Right heart catheterization revealed postcapillary pulmonary hypertension, with mean pulmonary artery pressure (mPA = 48 mmHg), pulmonary capillary wedge pressure (PCWP) of 25 mmHg, a significant left-to-right shunt (Qp/Qs = 2.5:1) and pulmonary vascular resistance (PVR) of 2 Wood units. Cardiac CT (<xref ref-type="fig" rid="f1"><bold>Figure 1</bold></xref>) showed a large communication around 3.3 cm in diameter between both atria as well as a dilated CS of 1.1 cm diameter. Transesophageal echocardiography (<xref ref-type="fig" rid="f2"><bold>Figure 2</bold></xref>, <xref ref-type="fig" rid="f3"><bold>Figure 3</bold></xref>) with bubble test disclosed a communication between the left atrium and the CS consistent with diagnosis of CS ASD without a persistent left superior vena cava (PLSVC). After intensification of diuretic therapy, follow-up catheterization 2 months later showed a reduction of PCWP (10mmHg) and mPA (25 mmHg) leading to successful surgical repair.</p>
<fig id="f1" position="float" fig-type="figure"><label>FIGURE 1</label><caption><p>Heart computed tomography.</p></caption><graphic xlink:href="CC202217_9-10_226-7-f1"></graphic></fig>
<fig id="f2" position="float" fig-type="figure"><label>FIGURE 2</label><caption><p>Transesophageal echocardiography.</p></caption><graphic xlink:href="CC202217_9-10_226-7-f2"></graphic></fig>
<fig id="f3" position="float" fig-type="figure"><label>FIGURE 3</label><caption><p>Transesophageal echocardiograph &#x2013; color Doppler.</p></caption><graphic xlink:href="CC202217_9-10_226-7-f3"></graphic></fig>
<p><bold>Conclusion</bold>: Patients with left-to-right shunts due to CS ASD are usually asymptomatic throughout adulthood. However, once symptoms occur, this congenital heart malformation remains often misdiagnosed. Therefore, we emphasize the importance of multimodal imaging in these patients (<xref ref-type="bibr" rid="r2"><italic>2</italic></xref>).</p>
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<ref-list>
<title>LITERATURE</title>
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