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Spontaneous Coronary Artery Dissection in a Young Women: A Case Report and Literature Review
Jiong Xiao1, Chaoyong He1, Yiyan Wang1
1Department of Cardiology, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, China.
Insights
Spontaneous coronary artery dissection (SCAD) involving the left main coronary artery (LMCA) is a critical condition. Prompt recognition and management are vital for patients presenting with SCAD, especially those experiencing severe symptoms.
Area of Science:
- Cardiology
- Vascular Medicine
Background:
- Spontaneous coronary artery dissection (SCAD) is a rare cause of acute coronary syndrome.
- Left main coronary artery (LMCA) SCAD is a particularly severe presentation.
- SCAD is defined by its non-atherosclerotic, non-traumatic, and non-iatrogenic origins.
Abstract:
Spontaneous coronary artery dissection (SCAD) is an infrequent etiology of acute coronary syndrome, characterized by its non-atherosclerotic, non-traumatic, and non-iatrogenic nature. SCAD involving the left main coronary artery (LMCA) constitutes an especially severe manifestation of this condition. This report details a complex and critical case of LMCA SCAD in a 38-year-old female patient who presented with chest pain, syncope, cardiogenic shock, severe hypokalemia, and electrocardiographic changes consistent with De Winter syndrome. Initial urgent coronary angiography (CAG) revealed LMCA stenosis of 40%-50%. Subsequent CAG, supplemented by intravascular ultrasound, demonstrated a progression of LMCA stenosis to 70%-80% and the presence of a diffuse intramural hematoma within the LMCA. Patients with LMCA SCAD are at a heightened risk for short-term complications. Therefore, prompt recognition and the implementation of appropriate management strategies are crucial.
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