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Spontaneous coronary artery dissection in a 27-year-old woman
Bart R Besinger1, Stephanie Gardner
1Department of Emergency Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Insights
Spontaneous coronary artery dissection (SCAD) is a critical cause of heart attacks in young adults. Systemic inflammatory diseases, like lupus, are increasingly recognized as potential risk factors for this condition.
Area of Science:
- Cardiology
- Rheumatology
Background:
- Spontaneous coronary artery dissection (SCAD) is a significant cause of acute coronary syndromes and sudden death, particularly in young individuals without traditional cardiovascular risk factors.
- Systemic inflammatory and connective tissue diseases are emerging as potential contributing factors to SCAD.
Observation:
- A case study details a 27-year-old woman with inflammatory arthropathy presenting with ST-elevation myocardial infarction.
- Coronary angiography confirmed SCAD; percutaneous coronary intervention was unsuccessful.
- The patient's recovery was achieved through medical management, followed by a diagnosis of systemic lupus erythematosus.
Findings:
- SCAD is an uncommon yet serious cause of acute coronary syndromes and sudden death.
- Young women are disproportionately affected by SCAD.
- While pregnancy is a known risk factor, systemic inflammatory and connective tissue diseases are also implicated.
Implications:
- Highlights the importance of considering systemic inflammatory and connective tissue diseases in the differential diagnosis of SCAD, especially in young women.
- Suggests a need for further research into the link between autoimmune conditions and SCAD.
- Emphasizes the role of medical management in SCAD cases where interventional procedures are not feasible or successful.
Background:
Spontaneous coronary artery dissection (SCAD) causes acute coronary syndromes or sudden death in young patients who are often lacking classic coronary disease risk factors. Systemic inflammatory and connective tissue diseases have been suggested as risk factors for SCAD.
Objective:
To review the risk factors, diagnosis, and management of this uncommon but life-threatening disease.
Case Report:
We report a case of a 27-year-old woman with a history of an ill-defined inflammatory arthropathy who presented with an acute ST-elevation myocardial infarction. SCAD was diagnosed by coronary angiography. Percutaneous coronary intervention was attempted but was unsuccessful. The patient recovered uneventfully with medical management and was ultimately diagnosed with systemic lupus erythematosus.
Conclusions:
SCAD is a rare but important cause of acute coronary syndromes and sudden death. It commonly occurs in young women. Although pregnancy is the most well-established risk factor, systemic inflammatory and connective tissue diseases have also been suggested as risk factors.
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