| Literature DB >> 19571766 |
Stelios Lampropoulos1, Efstratios K Theofilogiannakos, Argiris Gkontopoulos, Nikos P Kadoglou, Vassilis Mamalis, Theodosia Kontaki, George Kottas.
Abstract
Dissection of the innominate artery is extremely rare and is associated with a high in-hospital mortality rate. We present the case of a 44-year-old man who presented with syncope and cardiovocal syndrome as the result of a spontaneous innominate artery dissection with an extension to the right common carotid.Entities:
Mesh：
Year: 2009 PMID： 19571766 DOI： 10.2459/JCM.0b013e32832d2f31
Source DB: PubMed Journal: J Cardiovasc Med (Hagerstown) ISSN： 1558-2027 Impact factor: 2.160