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Spontaneous Coronary Artery Dissection With Systemic Lupus Erythematosus
Nourhan Chaaban1, Shilpa Kshatriya1,2
1Department of Internal Medicine, University of Kansas School of Medicine, Wichita, KS.
Spontaneous coronary artery dissection (SCAD) is a rare cause of heart attack, often linked to autoimmune conditions like systemic lupus erythematosus (SLE). Early diagnosis and treatment are crucial for better patient outcomes.
Area of Science:
- Cardiology
- Immunology
- Vascular Medicine
Background:
- Spontaneous coronary artery dissection (SCAD) is an uncommon cause of acute coronary syndrome (ACS) and sudden cardiac death.
- SCAD presentation ranges from asymptomatic to fatal, with associations noted for pregnancy and autoimmune diseases like systemic lupus erythematosus (SLE).
Observation:
- A 37-year-old female with hypertension, SLE, a history of preeclampsia, and smoking presented with chest pain.
- Elevated antiphospholipid antibodies (anti-β2-glycoprotein 1 IgG and positive lupus anticoagulant) were detected.
- Cardiac catheterization revealed spontaneous dissection with subintimal hematoma in the left anterior descending artery.
Findings:
- The patient experienced an acute coronary syndrome with elevated troponin levels.
- Successful stent placement was achieved via angioplasty.
- The case underscores the diagnostic challenges and the link between SCAD and SLE.
Implications:
- High index of suspicion is necessary for timely SCAD diagnosis.
- Recognizing the association between SCAD and autoimmune diseases like SLE can improve patient management.
- Early diagnosis and intervention in SCAD cases lead to improved clinical outcomes.
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