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Abdominal aorta aneurysms in children: single-center experience of six patients
Caisheng Ye1, Henghui Yin, Ying Lin
1Department of Vascular Surgery, First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Insights
Pediatric abdominal aortic aneurysms (AAA) are rare but serious. Prompt diagnosis and surgical repair using prosthetic grafts offer good outcomes in children, though recurrence is possible.
Area of Science:
- Vascular Surgery
- Pediatric Cardiology
- Medical Case Studies
Background:
- Abdominal aortic aneurysms (AAA) are uncommon in pediatric patients.
- AAA in children is associated with high morbidity and mortality.
- This study reviews the diagnosis and management of AAA in 6 pediatric cases.
Purpose of the Study:
- To summarize the institutional experience in diagnosing and managing pediatric abdominal aortic aneurysms.
- To evaluate the outcomes of surgical intervention for AAA in children.
Main Methods:
- Retrospective analysis of clinical data from 6 pediatric patients with AAA.
- Diagnostic tools included color Doppler ultrasonography and CT angiography.
- Surgical reconstruction involved aneurysm resection and prosthetic graft placement.
Main Results:
- Mean age at diagnosis was 8 years; all presented with pulsatile abdominal masses.
- Infrarenal AAAs were identified in all patients; causes were varied, including tuberous sclerosis and Takayasu's arteritis.
- Successful surgical reconstruction was achieved in all 6 cases with no immediate complications; one late recurrence led to mortality.
Conclusions:
- Prompt and accurate diagnosis is crucial for managing pediatric AAA.
- Surgical management with prosthetic grafts can yield favorable outcomes in children.
- Long-term surveillance is necessary due to the potential for aneurysm recurrence.
Background:
Abdominal aortic aneurysms (AAA) are rare in children and are associated with significant morbidity and mortality as in adults. We summarize our experience in the diagnosis and management of AAAs in 6 children at a single institution.
Methods:
The clinical data of 6 pediatric patients with AAAs treated at our hospital from November 2005 to November 2008 were retrospectively analyzed.
Results:
There were 4 males and 2 females with a mean age at diagnosis of 8 years (range, 17 months to 18 years). All patients presented with pulsatile abdominal masses. Color Doppler ultrasonography and computed tomography angiography were the primary diagnostic tools. One patient has a history of tuberous sclerosis, and 1 had Takayasu's arteritis; no risk factors or identifiable causes were found in the other patients. All of the AAAs identified were infrarenal. Surgical reconstruction with aneurysm resection and prosthetic graft placement was performed successfully in all 6 cases. No intraoperative or postoperative complications occurred. Mean follow-up has been 48 months (range, 32 to 69). In 1 patient, recurrence was noted at 3 years postoperatively. The patient's family declined further surgery, and the patient died, likely of rupture of the aneurysm at 41 months postoperatively. All other patients are currently alive and well.
Conclusions:
Our experience indicates that good outcomes can be obtained in children with AAAs with prompt and accurate diagnosis and surgical management with artificial grafts.
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