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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 2024 19_11-12_441</article-id>
<article-id pub-id-type="doi">10.15836/ccar2024.441</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Extended Abstract</subject></subj-group>
<subj-group subj-group-type="subheading"><subject>Heart failure</subject></subj-group>
</article-categories>
<title-group>
<article-title>Isolated cardiac sarcoidosis: a failed diagnosis?</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4842-7156</contrib-id><name><surname>Radi&#x0107;</surname><given-names>Petra</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/0000-0003-4719-4634</contrib-id><name><surname>Gabri&#x0107;</surname><given-names>Ivo 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/0000-0002-9707-6946</contrib-id><name><surname>Kordi&#x0107;</surname><given-names>Kre&#x0161;imir</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/0000-0002-0390-8466</contrib-id><name><surname>Hrabak-Paar</surname><given-names>Maja</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7116-2360</contrib-id><name><surname>Deli&#x0107;-Brklja&#x010D;i&#x0107;</surname><given-names>Diana</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib>
<contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9428-454X</contrib-id><name><surname>Trbu&#x0161;i&#x0107;</surname><given-names>Matias</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="aff" rid="aff3"><sup>3</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib>
<aff id="aff1"><label>1</label><institution>University Hospital Centre &#x201C;Sestre milosrdnice&#x201D; Zagreb</institution>, <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>
<aff id="aff3"><label>3</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>
</contrib-group>
<author-notes>
<corresp id="cor1"><label>*</label>ADDRESS FOR CORRESPONDENCE: Matias Trbu&#x0161;i&#x0107;, Klini&#x010D;ki bolni&#x010D;ki centar Sestre milosrdnice, Vinogradska cesta 29, HR-10000 Zagreb, Croatia. / Phone: +385-915062986 / E-mail: <email xlink:href="matias.trbusic@gmail.com">matias.trbusic@gmail.com</email></corresp></author-notes>
<pub-date date-type="pub" publication-format="electronic"><month>11</month><year>2024</year></pub-date>
<pub-date date-type="pub" publication-format="print"><month>11</month><year>2024</year></pub-date>
<volume>19</volume>
<issue>11-12</issue>
<fpage>441</fpage>
<lpage>441</lpage>
<history>
<date date-type="received"><day>13</day><month>10</month><year>2024</year></date>
<date><day>31</day><month>10</month><year>2024</year></date>
</history>
<permissions>
<copyright-statement>Croatian Cardiac Society</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Croatian Cardiac Society</copyright-holder>
</permissions>
<kwd-group kwd-group-type="author"><title>KEYWORDS: </title><kwd>cardiac sarcoidosis</kwd><kwd>heart failure</kwd><kwd>ventricular arrhythmias</kwd></kwd-group>
</article-meta>
</front>
<body>
<p><bold>Introduction:</bold> Isolated cardiac sarcoidosis (iCS) is an infiltrative cardiomyopathy that is the result of granulomatous inflammation that manifests predominantly in the myocardium. The annual incidence of sarcoidosis varies between 1 and 15 per 100,000 depending on the region (<xref ref-type="bibr" rid="r1"><italic>1</italic></xref>). The prevalence of iCS among patients with systemic sarcoidosis varies widely (23&#x2013;54%) because of differences in the definitions used (<xref ref-type="bibr" rid="r2"><italic>2</italic></xref>). Establishing a diagnosis of iCS is extremely difficult, since there is no unique echocardiographic, radiological or laboratory test to confirm the diagnosis. iCS may present with symptoms of heart failure, sudden cardiac death, ventricular arrhythmia, myocardial infarction or atrioventricular block (<xref ref-type="bibr" rid="r3"><italic>3</italic></xref>).</p>
<p><bold>Case report:</bold> 60-year-old female patient was recently hospitalized in our institution who presented with symptoms of heart failure without a history of previous cardiac diseases. Echocardiography showed a dilated left ventricle with hypokinesia of the basal segments of the septum, posterior, inferior and lateral walls with a reduced ejection fraction (EF) of 30%. Obstructive coronary artery disease was ruled out with coronary angiography. Cardiac magnetic resonance imaging (CMRI) was performed, which suspected the diagnosis of iCS. Positron emission tomography (PET) computed tomography (CT) showed increased metabolism of glucose analogues in the greater part of the left ventricle, which is consistent with iCS. Corticosteroid therapy was also introduced into the therapy in addition to the optimal medical therapy of heart failure. As part of the primary prevention of sudden cardiac death, a two-chamber ICD device was implanted.</p>
<p><bold>Conclusion:</bold> Patients with iCS have poor prognosis. If left untreated, iCS leads to progressive failure of the left ventricle with frequent ventricular arrhythmias and sudden cardiac death. iCS is a frequently misdiagnosed due its rarity and high index of suspicion needed to make the diagnosis. It should be noted that this is the only diagnosed case of iCS in the last 5 years in our institution, which, considering the incidence, leads us to the question of an adequate diagnosis confirmation. It is of utmost importance to increase the use of non-invasive diagnostic methods such as PET CT scan and CMRI to detect all patients with iCS.</p>
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<ref-list>
<title>LITERATURE</title>
<ref id="r1"><label>1</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Rossides</surname><given-names>M</given-names></name><name><surname>Darlington</surname><given-names>P</given-names></name><name><surname>Kullberg</surname><given-names>S</given-names></name><name><surname>Arkema</surname><given-names>EV</given-names></name></person-group>. <article-title>Sarcoidosis: Epidemiology and clinical insights.</article-title> <source>J Intern Med</source>. <year>2023</year>;<volume>293</volume>:<fpage>668</fpage>&#x2013;<lpage>80</lpage>. <pub-id pub-id-type="doi">10.1111/joim.13629</pub-id><pub-id pub-id-type="pmid">36872840</pub-id></mixed-citation></ref>
<ref id="r2"><label>2</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Okada</surname><given-names>DR</given-names></name><name><surname>Bravo</surname><given-names>PE</given-names></name><name><surname>Vita</surname><given-names>T</given-names></name><name><surname>Agarwal</surname><given-names>V</given-names></name><name><surname>Osborne</surname><given-names>MT</given-names></name><name><surname>Taqueti</surname><given-names>VR</given-names></name><etal/></person-group> <article-title>Isolated cardiac sarcoidosis: a focused review of an under&#x2010;recognized entity.</article-title> <source>J Nucl Cardiol</source>. <year>2018</year>;<volume>25</volume>:<fpage>1136</fpage>&#x2013;<lpage>46</lpage>. <pub-id pub-id-type="doi">10.1007/s12350-016-0658-1</pub-id><pub-id pub-id-type="pmid">27613395</pub-id></mixed-citation></ref>
<ref id="r3"><label>3</label><mixed-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Birnie</surname><given-names>DH</given-names></name><name><surname>Nery</surname><given-names>PB</given-names></name><name><surname>Ha</surname><given-names>AC</given-names></name><name><surname>Beanlands</surname><given-names>RS</given-names></name></person-group>. <article-title>Cardiac Sarcoidosis.</article-title> <source>J Am Coll Cardiol</source>. <year>2016</year> July 26;<volume>68</volume>(<issue>4</issue>):<fpage>411</fpage>&#x2013;<lpage>21</lpage>. <pub-id pub-id-type="doi">10.1016/j.jacc.2016.03.605</pub-id><pub-id pub-id-type="pmid">27443438</pub-id></mixed-citation></ref>
</ref-list>
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