<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>30(26)</volume><submitter>Kim DY</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Paragangliomas are rare neuroendocrine tumors arising from chromaffin cells, often associated with excess catecholamine production. Cardiac paragangliomas are particularly uncommon, accounting for &lt;1% of all cardiac tumors.&lt;h4>Case summary&lt;/h4>We report a case of a right ventricular mass that was initially misidentified as a pericardial cyst on imaging but was ultimately diagnosed as a benign paraganglioma deriving from hereditary paraganglioma and pheochromocytoma syndrome after further diagnostic evaluation and treatment.&lt;h4>Discussion&lt;/h4>This case highlights how rare pathologies may mimic other conditions, emphasizing the complexity and importance of a thorough diagnostic work-up in identifying cardiac paragangliomas.&lt;h4>Take-home messages&lt;/h4>Cardiac paragangliomas </pubmed_abstract><journal>JACC. Case reports</journal><pagination>104892</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12426667</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Right Ventricular Paraganglioma Mimicking Coronary Artery Aneurysm: A Diagnostic Conundrum.</pubmed_title><pmcid>PMC12426667</pmcid><pubmed_authors>Jenkins WT</pubmed_authors><pubmed_authors>Kim DY</pubmed_authors><pubmed_authors>Shah P</pubmed_authors><pubmed_authors>Prasad R</pubmed_authors><pubmed_authors>Anand U</pubmed_authors><pubmed_authors>Alkhatib D</pubmed_authors><pubmed_authors>Azarkhail R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Right Ventricular Paraganglioma Mimicking Coronary Artery Aneurysm: A Diagnostic Conundrum.</name><description>&lt;h4>Background&lt;/h4>Paragangliomas are rare neuroendocrine tumors arising from chromaffin cells, often associated with excess catecholamine production. Cardiac paragangliomas are particularly uncommon, accounting for &lt;1% of all cardiac tumors.&lt;h4>Case summary&lt;/h4>We report a case of a right ventricular mass that was initially misidentified as a pericardial cyst on imaging but was ultimately diagnosed as a benign paraganglioma deriving from hereditary paraganglioma and pheochromocytoma syndrome after further diagnostic evaluation and treatment.&lt;h4>Discussion&lt;/h4>This case highlights how rare pathologies may mimic other conditions, emphasizing the complexity and importance of a thorough diagnostic work-up in identifying cardiac paragangliomas.&lt;h4>Take-home messages&lt;/h4>Cardiac paragangliomas </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-04-08T19:12:36.973Z</modification><creation>2026-04-08T12:04:42.595Z</creation></dates><accession>S-EPMC12426667</accession><cross_references><pubmed>40912844</pubmed><doi>10.1016/j.jaccas.2025.104892</doi></cross_references></HashMap>