Percutaneous coronary intervention guided by CCTA successfully revascularized a rare anomalous LAD originating from the right coronary cusp, with the patient remaining free of MACE at 6 months.
Case Report (n=1)
No
This case highlights the procedural challenges of PCI in patients with rare coronary anomalies and the utility of CCTA in defining the coronary course to guide safe intervention.
Abstract Coronary artery anomalies are rare congenital conditions with a prevalence of <1% in the general population. We describe a 61-year-old male who presented with acute coronary syndrome (ACS) and Type A Wellens syndrome. Coronary angiography demonstrated an extremely rare anomaly in which all three coronary arteries originated from the right coronary cusp with separate ostia. Coronary computed tomography angiography (CCTA) further delineated a benign retroaortic course of the left anterior descending artery (LAD). Percutaneous coronary intervention was performed via a right transfemoral approach using a Judkins Right 7F catheter, achieving successful revascularization of the culprit LAD lesion. The patient recovered uneventfully and remained free of major adverse cardiac events at 6-month follow-up. This case underscores the procedural challenges posed by anomalous coronary anatomy and highlights the critical role of computed tomography imaging in defining the coronary course and guiding safe intervention. When an anomalous coronary origin is suspected during ACS evaluation, urgent CCTA may be useful to define the coronary course before revascularization in selected cases. The combination of all three coronary arteries arising from the right coronary cusp, along with a retroaortic LAD course, emphasizes the rarity and clinical relevance of this presentation.
Hesarur et al. (Thu,) conducted a case report in Acute coronary syndrome and coronary artery anomaly (n=1). Percutaneous coronary intervention and CCTA was evaluated on Major adverse cardiac events. Percutaneous coronary intervention guided by CCTA successfully revascularized a rare anomalous LAD originating from the right coronary cusp, with the patient remaining free of MACE at 6 months.