Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/41956
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dc.contributor.authorMarshall, D.-
dc.contributor.authorGilbert, J.-
dc.contributor.authorByard, R.-
dc.date.issued2007-
dc.identifier.citationForensic Science Medicine and Pathology, 2007; 3(1):53-56-
dc.identifier.issn1547-769X-
dc.identifier.issn1556-2891-
dc.identifier.urihttp://hdl.handle.net/2440/41956-
dc.description.abstractA 26-year-old man who presented with a 2-year history of intermittent gynecomastia with recent onset of fever, night sweats, and abdominal distension was found to have a left-sided adrenocortical carcinoma with metastases to the liver and spine. Sudden death occurred 1 month after his presentation. At autopsy a saddle pulmonary thromboembolus was found occluding the pulmonary outflow tract, with smaller more peripheral pulmonary thromboemboli. No tumor deposits were identified in the thromboemboli. The thromboemboli had arisen from a tongue of tumor that had grown through the left adrenal vein into the inferior vena cava. Despite a high rate of angio-invasion there are very few reports of sudden death resulting from this phenomenon in patients with adrenocortical carcinoma.-
dc.description.statementofresponsibilityDrew T. Marshall, John D. Gilbert and Roger W. Byard-
dc.language.isoen-
dc.publisherHumana Press, Inc.-
dc.titleAdrenocortical carcinoma and sudden death-
dc.typeJournal article-
dc.identifier.doi10.1385/FSMP:3:1:53-
pubs.publication-statusPublished-
dc.identifier.orcidByard, R. [0000-0002-0524-5942]-
Appears in Collections:Aurora harvest 6
Pathology publications

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