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Updated: Jan 24, 2026

A New Murine Model of Endovascular Aortic Aneurysm Repair
Published on: July 7, 2013
A Successful Repair of Pseudocoarctation With Associated Aortic Arch Aneurysm in an Eight-Month-Old Infant
Roman Sekelyk1, Zufar Abdurakhmanov1, Andrii Kurkevych2
1Department of Cardiac Surgery of Newborns and Early Childhood, Ukrainian Children's Cardiac Center, Kyiv, Ukraine.
Insights
This study presents a rare case of pseudocoarctation of the aorta in an infant, successfully treated with surgical aortic arch reconstruction. The procedure avoided prosthetic use, ensuring a favorable outcome.
Area of Science:
- Cardiovascular Surgery
- Pediatric Cardiology
- Medical Imaging
Background:
- Pseudocoarctation of the aorta is a rare congenital anomaly.
- Characterized by aortic arch elongation and tortuosity, often associated with aneurysms.
Purpose of the Study:
- To report a successful surgical management of pseudocoarctation of the aorta in a pediatric patient.
- To highlight the use of advanced imaging and a prosthesis-free reconstruction technique.
Main Methods:
- Prenatal diagnosis using magnetic resonance imaging.
- Postnatal confirmation with computed tomography angiography.
- Surgical resection of the aneurysmal aorta with extended end-to-end reconstruction and left subclavian artery reimplantation.
Main Results:
- The infant underwent successful aortic arch reconstruction without prosthetic material.
- Postoperative imaging confirmed no residual stenosis at six months.
- The patient experienced an uneventful recovery.
Conclusions:
- Surgical repair of pseudocoarctation of the aorta is feasible and effective in infants.
- Prosthesis-free reconstruction is a viable option for managing this condition.
- Early diagnosis and timely intervention are crucial for optimal outcomes.
Abstract:
Pseudocoarctation of the aorta is an uncommon congenital entity characterized by juxtaductal elongation and tortuosity of the aortic arch. It is known to be associated with aneurysm formation. Our patient is a 7.7-month-female infant followed prenatally by magnetic resonance imaging that detected this anomaly. Subsequently, postnatal preoperative computed tomography angiography was confirmatory. The operation comprised resection of the aneurysmal portion of the aorta and extended end-to-end reconstruction, without prosthesis usage. The left subclavian artery was reimplanted into the left carotid artery. The postoperative course was uneventful. Computed tomography aortography and transthoracic echocardiography demonstrated no residual stenosis at six months of follow-up.
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