| Literature DB >> 12848802 |
Ertan Okmen1, Izzet Erdinler, Enis Oguz, Ahmet Akyol, Nese Cam.
Abstract
Vagal paraganglioma is one of the rare tumors of the neuroendocrine system. We are reporting a vagal paraganglioma case presented with uncommon features of the disease: asystole and syncope. Syncope episodes occurred 3 years before the major symptoms of the disease. Dual chamber pacemaker failed to prevent syncope attacks because of the vasodepressor component. The patient was treated successfully with en bloc removal of tumor and vagal nerve. Syncope episodes disappeared after operation.Entities:
Mesh:
Year: 2003 PMID: 12848802 PMCID: PMC6932380 DOI: 10.1046/j.1542-474x.2003.08215.x
Source DB: PubMed Journal: Ann Noninvasive Electrocardiol ISSN: 1082-720X Impact factor: 1.468