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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_572</article-id>
<article-id pub-id-type="doi">10.15836/ccar2024.572</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Extended Abstract</subject></subj-group>
<subj-group subj-group-type="subheading"><subject>Intensive and acute cardiac care</subject></subj-group>
</article-categories>
<title-group>
<article-title>Right atrial myxoma in a patient with Carney syndrome: a case report</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5441-0900</contrib-id><name><surname>Hr&#x017E;i&#x0107;</surname><given-names>Biljana</given-names></name><xref ref-type="corresp" rid="cor1">*</xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2975-8793</contrib-id><name><surname>Slamek</surname><given-names>Nikolina</given-names></name></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6421-6471</contrib-id><name><surname>Grandavec</surname><given-names>Katarina</given-names></name></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0006-1973-8509</contrib-id><name><surname>Vidak</surname><given-names>Martina</given-names></name></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0008-8617-9932</contrib-id><name><surname>Ku&#x0161;eni&#x0107;</surname><given-names>Petra</given-names></name></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7402-8135</contrib-id><name><surname>Kuni&#x0107;</surname><given-names>Magdalena</given-names></name></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1878-0880</contrib-id><name><surname>Benko</surname><given-names>Ivica</given-names></name></contrib>
<aff id="aff1"><institution>Dubrava University Hospital</institution>, <addr-line>Zagreb</addr-line>, <country country="hr">Croatia</country></aff>
</contrib-group>
<author-notes>
<corresp id="cor1"><label>*</label>ADDRESS FOR CORRESPONDENCE: Biljana Hr&#x017E;i&#x0107;, Klini&#x010D;ka bolnica Dubrava, Avenija Gojka &#x0160;u&#x0161;ka 6, HR-10000 Zagreb, Croatia. / Phone: +385-1-5540-677 / E-mail: <email xlink:href="bhrzic@kbd.hr">bhrzic@kbd.hr</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>572</fpage>
<lpage>572</lpage>
<history>
<date date-type="received"><day>20</day><month>09</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>Carney complex</kwd><kwd>cardiac myxomas</kwd></kwd-group>
</article-meta>
</front>
<body>
<p><bold>Introduction</bold>: Carney Complex (CNC) is a rare, autosomal dominant genetic syndrome characterized by the development of benign connective tissue tumors (myxomas), skin pigmentation changes, endocrine abnormalities, and tumors in other tissues. This syndrome is associated with mutations in the PRKAR1A gene, which plays a crucial role in the regulation of cellular growth. Cardiac myxomas are rare in the general population, with an incidence of 0.5&#x2013;1 per million people per year, but they are frequently observed in patients with Carney Complex, appearing in 20&#x2013;40% of cases. These myxomas are a leading cause of death among CNC patients, often being multiple and sometimes present at birth. Recurrence of myxomas in these patients is linked to the excessive secretion of growth hormone. Surgical treatment is the primary therapeutic approach for atrial myxomas, and regular follow-up is essential for preventing complications and managing the risk of recurrence. (<xref ref-type="bibr" rid="r1"><italic>1</italic></xref>, <xref ref-type="bibr" rid="r2"><italic>2</italic></xref>)</p>
<p><bold>Case report</bold>: This case involves a 46-year-old female patient who was hospitalized due to a tumor in the left atrium. She had a history of Hashimoto&#x2019;s thyroiditis, iron deficiency anemia, and mild allergic asthma. The tumor, measuring 37x47 mm, was attached by a stalk to the interatrial septum, and was diagnosed at another healthcare facility. Clinical signs and symptoms raised suspicion of Carney Complex, leading to a thorough endocrinological evaluation. After a cardiology and cardiothoracic surgery consultation, surgical intervention was deemed the optimal treatment approach. The surgery was successfully performed, and the patient was discharged in good condition with recommendations for ongoing follow-up.</p>
<p><bold>Conclusion</bold>: Nursing care for patients with atrial myxomas and Carney Complex requires a specialized, individualized approach due to the complexity of the condition. It is crucial to recognize symptoms early, provide necessary support, and ensure a safe recovery. The focus is on continuous assessment, multidisciplinary collaboration, and patient support to minimize the risk of complications and achieve optimal treatment outcomes.</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>Pitsava</surname><given-names>G</given-names></name><name><surname>Zhu</surname><given-names>C</given-names></name><name><surname>Sundaram</surname><given-names>R</given-names></name><name><surname>Mills</surname><given-names>JL</given-names></name><name><surname>Stratakis</surname><given-names>CA</given-names></name></person-group>. <article-title>Predicting the risk of cardiac myxoma in Carney complex.</article-title> <source>Genet Med</source>. <year>2021</year> January;<volume>23</volume>(<issue>1</issue>):<fpage>80</fpage>&#x2013;<lpage>5</lpage>. <pub-id pub-id-type="doi">10.1038/s41436-020-00956-3</pub-id><pub-id pub-id-type="pmid">32893266</pub-id></mixed-citation></ref>
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