{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,11]],"date-time":"2026-05-11T13:15:05Z","timestamp":1778505305695,"version":"3.51.4"},"reference-count":15,"publisher":"SAGE Publications","license":[{"start":{"date-parts":[[2019,1,1]],"date-time":"2019-01-01T00:00:00Z","timestamp":1546300800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["SAGE Open Medical Case Reports"],"published-print":{"date-parts":[[2019,1]]},"abstract":"<jats:p> Functional paragangliomas are rare neuroendocrine tumours that secrete catecholamines and are infrequently found in the mediastinum. We report a case of a young male with symptoms of catecholamine excess and a personal and family history of the paraganglioma predisposing succinate dehydrogenase subunit B mutation. The lesion had anatomical intrapericardial juxtaposition to important cardiac anatomy and posed the significant challenge of dissection at surgery. The lesion was successfully resected via sternotomy on cardiopulmonary bypass and confirmed histopathologically as paraganglioma. Intrapericardial paraganglioma is rare and treatment is difficult and time critical considering the proximity of cardiac anatomy as well as malignant potential. <\/jats:p>","DOI":"10.1177\/2050313x19839530","type":"journal-article","created":{"date-parts":[[2019,4,1]],"date-time":"2019-04-01T09:57:48Z","timestamp":1554112668000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":5,"title":["Resection of a functioning intrapericardial paraganglioma associated with succinate dehydrogenase B mutation"],"prefix":"10.1177","volume":"7","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-1080-4451","authenticated-orcid":false,"given":"Dylan A","family":"Siejka","sequence":"first","affiliation":[{"name":"Tasmanian Cardiothoracic Unit, Royal Hobart Hospital, Hobart, TAS, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alexander F","family":"Vittorio","sequence":"additional","affiliation":[{"name":"Tasmanian Cardiothoracic Unit, Royal Hobart Hospital, Hobart, TAS, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sameer","family":"Thakur","sequence":"additional","affiliation":[{"name":"Tasmanian Cardiothoracic Unit, Royal Hobart Hospital, Hobart, TAS, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John R","family":"Burgess","sequence":"additional","affiliation":[{"name":"Department of Endocrinology, Royal Hobart Hospital, Hobart, TAS, Australia"},{"name":"School of Medicine, University of Tasmania, Hobart, TAS, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ashutosh","family":"Hardikar","sequence":"additional","affiliation":[{"name":"Tasmanian Cardiothoracic Unit, Royal Hobart Hospital, Hobart, TAS, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2019,4,1]]},"reference":[{"issue":"3","key":"bibr1-2050313X19839530","first-page":"276","volume":"13","author":"Michalowska I","year":"2016","journal-title":"Kardiochir Torakochirurgia Pol"},{"key":"bibr2-2050313X19839530","doi-asserted-by":"publisher","DOI":"10.1186\/1749-8090-8-22"},{"key":"bibr3-2050313X19839530","doi-asserted-by":"publisher","DOI":"10.1111\/jocs.12455"},{"key":"bibr4-2050313X19839530","doi-asserted-by":"publisher","DOI":"10.1002\/hed.23098"},{"key":"bibr5-2050313X19839530","doi-asserted-by":"crossref","unstructured":"Samuel N, Ejaz R, Silver J, et al. 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