An Unusual Case of Chronic Total Occlusion Secondary to Late-Diagnosed Recurrent Spontaneous Coronary Dissection
Gianluca Castaldi1, Yves de Greef1, Alice Benedetti1
1Hartcentrum, Ziekenhuis Netwerk Antwerpen (ZNA) Middelheim, Antwerp, Belgium.
Insights
Spontaneous coronary artery dissection (SCAD) is a rare cause of acute coronary syndrome, particularly in men. High suspicion is crucial for early diagnosis and effective treatment, as missed diagnoses can lead to severe outcomes.
Area of Science:
- Cardiology
- Vascular Medicine
Background:
- Spontaneous coronary artery dissection (SCAD) is an uncommon cause of acute coronary syndrome (ACS).
- SCAD is even rarer in male patients compared to females.
- A high index of suspicion is necessary for timely diagnosis in patients presenting with ACS, especially younger individuals without traditional cardiovascular risk factors.
Observation:
- A 44-year-old male with a history of revascularization procedures presented with worsening exertional angina.
- Initial assessment revealed a "dynamic total occlusion" of the left circumflex coronary artery.
- This finding was ultimately diagnosed as an unrecognized spontaneous coronary artery dissection.
Findings:
- The case underscores that SCAD can present atypically, even in patients with prior cardiac interventions.
- Missed or delayed diagnosis of SCAD can result in significant adverse cardiovascular events.
- Intravascular imaging modalities are vital for confirming the diagnosis of SCAD.
Implications:
- This case highlights the importance of considering SCAD in the differential diagnosis of ACS, irrespective of patient demographics or history.
- Prompt and accurate diagnosis of SCAD is essential for appropriate management and to prevent complications.
- The utility of intravascular imaging in diagnosing SCAD, particularly in complex cases, is emphasized.
Abstract:
We report a case of a male patient, aged 44 years, with a long history of percutaneous and surgical revascularizations, who presented with progressive effort angina and a "dynamic total occlusion" of the left circumflex coronary artery, which turned out to be an unrecognized spontaneous coronary artery dissection. In conclusion, spontaneous coronary artery dissection is a rare cause of acute coronary syndrome and it is even less frequent in male patients; therefore, a high level of suspicion, especially in the case of young patients without major cardiovascular risk factors, is mandatory for prompt diagnosis and adequate strategy. Our case highlights how a missed proper initial diagnosis can dramatically evolve. Furthermore, intravascular imaging can be crucial for confirming the diagnosis.
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