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Echocardiographic Assessment of the Right Heart in Mice
Published on: November 27, 2013
Five chambered heart: a case report and brief review of literature
Ozer Badak1, Bahri Akdeniz, Ozhan Goldeli
1Department of Cardiology, School of Medicine, Dokuz Eylul University, 35340, Inciralti, Izmir, Turkey. ozer.badak@deu.edu.tr
Insights
A rare congenital heart anomaly presented as chest pain and suspicious ischemia findings. Diagnostic imaging revealed a dilated left anterior descending coronary artery with an unusual fistulous connection to a septal chamber.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Medical Imaging
Background:
- Myocardial ischemia can present with diverse etiologies.
- Congenital coronary artery anomalies are uncommon but clinically significant.
- Diagnostic challenges arise in identifying complex cardiac malformations.
Observation:
- A patient presented with chest pain and initial findings suggestive of myocardial ischemia.
- Electrocardiography and myocardial perfusion scintigraphy indicated potential coronary artery issues.
- Further investigations included coronary angiography, echocardiography, and magnetic resonance imaging.
Findings:
- A dilated left anterior descending coronary artery was identified.
- This artery demonstrated a fistulous communication with a distinct chamber.
- The anomalous chamber was located within the infero-apical interventricular septum.
Implications:
- This case highlights a complex congenital anomaly requiring careful diagnostic evaluation.
- Understanding such anomalies is crucial for accurate diagnosis and management.
- The report discusses the clinical challenges posed by this rare cardiac malformation.
Abstract:
We present a patient with chest pain and suspicious findings in electrocardiography and myocardial perfusion scintigraphy for myocardial ischemia. Coronary angiography and then echocardiography and magnetic resonance imaging revealed a dilated left anterior descending coronary artery, which has fistulous communication with a large, separate chamber that occupies the infero-apical interventricular septum. This is a challenging congenital anomaly for a clinician in many aspects, which are discussed in the report.
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