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									<identifier>oai:www.peertechzpublications.org:10.17352/2455-5452.000013</identifier>
									<datestamp>2016-06-29</datestamp>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										An Atypical Giant Right Atrial Myxoma Presented with Minimal Symptoms
										</dc:title><dc:creator>Huseyın Goksuluk</dc:creator><dc:creator> Orhan Veli Doğan</dc:creator><dc:creator> Barbaros Dokumacı</dc:creator><dc:creator>Ilker Ozer</dc:creator><dc:description>&lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;Primary tumours of the heart are not common and the prevalence of cardiac tumors ranges from 0,001% to 0,3% at autopsy [1]. Over 70% of primary cardiac tumors are benign and the most common form of these primary tumours are myxomas. Most of the myxomas are located in the left atrium (%75–80), arising from the interatrial septum at the border of the fossa ovalis [2]. Larger tumors are more likely to be associated with cardiovascular symptoms [3]. Commonly observed symptoms and signs are dyspnea, pulmonary edema, cough, peripheral edema and fatigue. Constitutional symptoms (fever, weight loss) are seen in around 30% of patients. Laboratory abnormalities (anemia and elevations in the erythrocyte sedimentation rate, C-reactive protein) are present in 35 % of patients [4].&lt;/p&gt;&lt;p&gt;This case report show us discrepancy between giant right atrial myxoma and atypical symptom of patient. Once a cardiac myxoma is diagnosed, surgical excision should be performed without delays because of the risk of thromboembolic events [5-7], syncope and sudden cardiac death. Generally, surgical treatment is definitive and recurrence is uncommon.&lt;/p&gt;</dc:description>
										<dc:publisher>International Journal of Vascular Surgery and Medicine - Peertechz Publications</dc:publisher>
										<dc:date>2016-06-29</dc:date>
										<dc:type>Case Report</dc:type>
										<dc:identifier>https://doi.org/10.17352/2455-5452.000013</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Huseyın Goksuluk et al.</dc:rights>
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