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Spontaneous coronary artery dissection associated with Leriche syndrome
C Y Karabay1, M M Can, I H Tanboga
1Cardiology Clinic, Kartal Kosuyolu Heart and Research Hospital, Istanbul, Turkey. karabaymd@yahoo.com
Insights
Spontaneous coronary artery dissection (SCAD) is a rare cause of acute coronary syndrome. This case highlights SCAD occurring alongside Leriche syndrome in a middle-aged man.
Area of Science:
- Cardiology
- Vascular Medicine
Background:
- Spontaneous coronary artery dissection (SCAD) is an uncommon cause of acute coronary syndrome.
- SCAD typically affects patients with coronary atherosclerosis, women in the peripartum period, or those with idiopathic causes.
Observation:
- A 44-year-old male patient presented with SCAD.
- The patient also had Leriche syndrome, a rare condition involving the blockage of the abdominal aorta and iliac arteries.
Findings:
- This case report details the rare concurrence of SCAD and Leriche syndrome in a male patient.
- SCAD can be associated with other vascular conditions beyond its typical patient profiles.
Implications:
- The findings suggest a potential link between SCAD and other forms of arterial disease.
- Further research is warranted to understand the underlying mechanisms and associations of SCAD with conditions like Leriche syndrome.
Abstract:
Spontaneous coronary artery dissection (SCAD) is a rare cause of acute coronary syndrome. SCAD has been observed in three groups of patients; those with coronary atherosclerosis, women in the peripartum period, and those with an idiopathic cause. SCAD may also be associated with other conditions. Herein, we present a 44-year-old man who developed SCAD concomitant with Leriche syndrome.
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