Spontaneous Coronary Artery Dissection: An Under-recognized Cause of Acute Coronary Syndromes
Hanan Al Naabi1, Hatim Al Lawati2
1Internal Medicine Residency Program, Oman Medical Specialty Board, Muscat, Oman.
Insights
Spontaneous coronary artery dissection (SCAD) is a rare condition. This case study shows complete resolution of type 2 SCAD after conservative management, highlighting SCAD
Area of Science:
- Cardiology
- Vascular Medicine
Background:
- Spontaneous coronary artery dissection (SCAD) is a rare cause of acute coronary syndrome.
- Diagnosis is challenging due to limitations of conventional angiography.
- Management strategies for SCAD are not well-established.
Observation:
- A 55-year-old woman presented with acute coronary syndrome.
- Coronary angiography revealed type 2 SCAD.
- The patient was managed conservatively.
Findings:
- Repeat angiography three months later showed complete resolution of the SCAD.
- Cross-sectional imaging ruled out underlying fibromuscular dysplasia (FMD).
- The patient experienced no recurrence during follow-up.
Implications:
- Conservative management can lead to SCAD resolution.
- SCAD may occur independently of fibromuscular dysplasia.
- This case contributes to understanding SCAD natural history and management.
Abstract:
Spontaneous coronary artery dissection (SCAD) is a rare condition that is often underdiagnosed given limitations of conventional cineangiography. In addition to the diagnostic challenge, the condition poses a major therapeutic dilemma given paucity of literature to guide management. We report the case of a 55-year-old woman, who presented with acute coronary syndrome. Coronary angiography at the time of the index hospitalization revealed type 2 SCAD. She was managed conservatively. Repeat coronary angiography three months later showed complete resolution of the previously noted dissection. Because of the high association between SCAD and fibromuscular dysplasia (FMD), a cross-sectional imaging was performed in this case, which ruled out underlying FMD. The patient has been followed longitudinally since her index event and has had no reported recurrences.
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