| Literature DB >> 17389210 |
Andres Beiras-Fernandez1, Peter Uberfuhr, Ingo Kaczmarek, Konstantinou Nikolaou, Florian Weis, Theodor Ramp, Peter Lamm, Eckart Kreuzer, Bruno Reichart.
Abstract
Primary pheochromocytomas located outside the adrenal glands account for only 10% of all pheochromocytomas. Mediastinal pheochromocytomas are even rarer and usually represent a therapeutic challenge as they often infiltrate adjacent structures. We report the case of a large primary mediastinal pheochromocytoma in a 65-year-old patient presenting with a sudden angina-like chest pain and dyspnea. Thoracic multislice computed tomography showed an 8 x 5 x 6-cm retrocardiac mass causing compression of both atria and infiltrating the left superior pulmonary vein. The tumor was highly vascularized and presented a blood supply derived from the circumflex artery. The mass was successfully removed by open heart surgery, and the patient was discharged 10 days postoperatively.Entities:
Mesh:
Year: 2007 PMID: 17389210 DOI: 10.1532/HSF98.20071008
Source DB: PubMed Journal: Heart Surg Forum ISSN: 1098-3511 Impact factor: 0.676