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A Novel Murine Model of Arteriovenous Fistula Failure: The Surgical Procedure in Detail
Published on: February 3, 2016
Prenatal diagnosis of isolated coronary arteriovenous fistula
Uisoo Chae1, Mi-Young Lee1, Hyerim Kim1
1Department of Obstetrics and Gynecology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
Insights
A rare coronary arteriovenous fistula (CAVF) was diagnosed prenatally using fetal echocardiography. This early detection enabled timely surgical intervention, leading to a healthy outcome for the neonate.
Area of Science:
- Cardiology
- Fetal Medicine
- Pediatric Surgery
Background:
- Coronary arteriovenous fistula (CAVF) is a rare anomaly of coronary artery termination.
- Etiologies include congenital and acquired causes, with iatrogenic origins common post-cardiac procedures.
- Prenatal diagnosis of CAVF is infrequent, often associated with complex congenital heart disease.
Observation:
- An isolated coronary arteriovenous fistula was successfully diagnosed via fetal echocardiography at 25.3 weeks of gestation.
- This case represents a rare instance of an isolated CAVF identified prenatally.
Findings:
- Accurate prenatal diagnosis of isolated CAVF was achieved.
- The diagnosis facilitated prompt surgical planning and intervention.
Implications:
- Early and accurate prenatal diagnosis of CAVF is crucial for timely management.
- Successful surgical correction postnatally leads to favorable outcomes in neonates.
- This case highlights the importance of fetal echocardiography in identifying rare cardiac anomalies.
Abstract:
Coronary arteriovenous fistula (CAVF) is a rare condition defined as an anomalous termination of the coronary arteries. The etiology of CAVF is either congenital or acquired, and iatrogenic CAVF is most commonly caused by cardiovascular surgery or percutaneous intervention. Most of the prenatally diagnosed CAVFs were related to complex heart disease, and only few cases of an isolated CAVF have been reported to date. We successfully diagnosed an isolated CAVF by fetal echocardiography at 25.3 weeks of gestation. Accurate prenatal diagnosis resulted in the prompt decision for postnatal surgical correction, and the neonate thrived well without any complications.
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