Anomalous origin of the left coronary artery from pulmonary artery mimicking antero-lateral ST-elevation myocardial infarction: a case report
2024
Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery: A Case Report
Sample size: 1
publication
Evidence: low
Author Information
Author(s): Ziad Arow, Liaz Zilberman, Edward Koifman, Abid Assali, Yoav Arnson
Primary Institution: Meir Medical Center, Israel
Conclusion
ALCAPA in adulthood is a rare congenital anomaly that can be treated effectively with direct re-implantation of the LCA to the aorta.
Supporting Evidence
- ALCAPA is a rare congenital abnormality associated with early infant mortality.
- Only 10% of undiagnosed patients survive into adulthood.
- The average age of diagnosis in adulthood is 41 years.
- Advanced cardiac imaging can facilitate the diagnosis of ALCAPA.
Takeaway
A 25-year-old man had a rare heart problem where a main artery was connected to the wrong place, but doctors fixed it, and he is doing better now.
Methodology
The case involved a 25-year-old male diagnosed with ALCAPA through various imaging techniques including echocardiography, coronary angiography, and cardiac MRI.
Limitations
The study is based on a single case report, limiting generalizability.
Participant Demographics
25-year-old Arab male with no past medical history.
Digital Object Identifier (DOI)
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