Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery: A Case Report
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 successfully treated 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 patient presented with sudden cardiac arrest and was diagnosed using advanced imaging techniques.
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 who underwent various diagnostic tests including echocardiography, coronary angiography, and cardiac magnetic resonance imaging, followed by surgical repair.
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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