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Syncope and cardiovocal syndrome as the result of a spontaneous innominate artery dissection
Stelios Lampropoulos1, Efstratios K Theofilogiannakos, Argiris Gkontopoulos
1aDepartment of Cardiology, Mamatseio General Hospital, Kozani, Greece.
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.
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