Acute Coronary Syndrome Combined with Aortic Dissection Type A

Case Report

Austin J Clin Case Rep. 2022; 9(6): 1262.

Acute Coronary Syndrome Combined with Aortic Dissection Type A

Simoglou C¹* and Bertus I²

¹Cardiothoracic Department Hippocratio General Hospital Athens, Greece

²Department of Cardiothoracic Surgery, University of Bristol, School of Medicine, UK

*Corresponding author: Christos Simoglou, Cardiothoracic Department Hippocratio General Hospital Athens, Greece

Received: September 05, 2022; Accepted: October 06, 2022; Published: October 13, 2022

Abstract

We are presenting a case of Stanford Type a aortic dissection in a 58 year old male patient with history hypertension. He arrived at Emergency Department (ED) with diagnosis acute coronary syndrome a few hours after he developed sudden, severe worsening of his epigastric pain. Interesting case where the separation starts from the orifice of the right coronary artery, occupies the aortic valve.

Keywords: Stanford A; Aneurysm; Cardiothoracic diseases; Marfan’s syndrome; De Bakey classification

Introduction

Aortic dissection is one of the acute aortic syndromes and a type of arterial dissection. It occurs when blood enters the medial layer of the aortic wall through a tear or penetrating ulcer in the intima and tracks along the media, forming a second blood-filled channel within the wall [1]. Thoracic dissection is commonly divided according to the Stanford classification into type A (involving the descending thoracic aorta only) and type B (involving the descending thoracic aorta only). The main cause of dissection are hypertension, atherosclerosis, Marfan’s syndrome, Ehlers-Danlos syndrome, vasculitis, pregnancy and iatrogenic (aortic catheterization). The separation of the layers of the aortic wall produces a false channel, which spirals throughout a portion or commonly, the entire length of the aorta. In the United States, the prevalence of aortic dissection ranges from 0.2 to 0.8 per 100,000 per year or roughly 2,000 to 3,000 new cases per year [2].

Complications

Complications of aortic dissection include dissection and occlusion of branch vessels, distal thromboembolism, aneurismal dilatation and aortic rupture. Type A dissection may also result in coronary artery occlusion, aortic regurgitation and pericardial tamponade and therefore management of this type of dissection is usually emergency surgical repair. Type B dissections are usually managed with aggressive blood pressure control unless there are complications. An acute aortic dissection usually causes a severe sharp, tearing pain in the chest and upper back. In certain patients, the pain may develop or concentrate in the abdomen. In a very small number of patients, they may have little to no symptoms or flu-like symptoms (Figure 1). The weakening of the aortic wall can lead to aortic rupture within minutes or hours of the acute event [3]. The presence of the false channel in the ascending aorta can result in regurgitation of the aortic valve and myocardial infarction (heart attack). If the disturbance of aortic valve is significant this can lead to sudden symptoms of heart failure secondary to severe aortic valve regurgitation [4].