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A young female with an unusual cause of dyspnea
Insights
Coronary artery fistulas (CAFs) are abnormal connections between coronary arteries and heart chambers or vessels. This case highlights an unusual cause of dyspnea due to a right coronary artery fistula to the right atrium.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Medical Imaging
Background:
- Coronary artery fistulas (CAFs) are rare congenital or acquired abnormalities.
- They represent abnormal communications between a coronary artery and a heart chamber or systemic/pulmonary vessel.
- CAF prevalence is estimated at 0.08-0.4% of congenital cardiac anomalies.
Observation:
- A female patient presented with dyspnea and a continuous heart murmur.
- Cardiac catheterization revealed a fistula originating from the right coronary artery.
- The fistula showed flow directed towards the right atrium and right atrial appendage.
Findings:
- The identified fistula represents an unusual cause of dyspnea.
- Right coronary artery fistulas are common, but this specific termination is noteworthy.
- The continuous murmur indicated abnormal blood flow, consistent with a fistula.
Implications:
- Accurate diagnosis of CAFs is crucial, as some can be life-threatening.
- Understanding fistula termination is key to predicting clinical outcomes.
- This case underscores the importance of thorough cardiac evaluation for unexplained symptoms.
Abstract:
Within the context of coronary artery anomalies, coronary fistulas are classified by termination. A coronary artery fistula (CAF) involves a sizable communication between a coronary artery and a heart chamber (coronary-cameral fistula) or a segment of the systemic or pulmonary system (coronary artery arteriovenous fistula). These are often due to deviations from normal embryological development. CAF may be present in patients at any age, but is usually suspected in early childhood and accounts for 0.08-0.4% of congenital cardiac anomalies. They may also be acquired by trauma or from invasive cardiac procedures. The majority of CAF arises from the right coronary artery (55%) and the left anterior descending coronary artery, with the circumflex rarely involved. The outcome of these connections depends upon the termination site. The pathophysiology of these lesions is identical. Coronary artery anomalies are difficult to detect clinically. Most are benign but some may produce symptoms that can be life threatening. We present a female with an unusual cause of dyspnea found to have a continuous heart murmur, cardiac catheterization showed an evidence of a long tract arising from the origin of the right coronary artery with flow directed towards the right atrium and the right atrial appendage.
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