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Mycotic Saccular Abdominal Aortic Aneurysm in an Infant after Cardiac Catheterization: A Case Report
Ehsan Benrashid1, Christopher C McCoy1, Henry E Rice2
1Division of Vascular Surgery, Department of Surgery, Duke University Medical Center, Durham, NC.
Insights
A rare pediatric mycotic abdominal aortic aneurysm (AAA) was found in an infant after cardiac surgery. Surgical repair successfully resolved the life-threatening condition.
Area of Science:
- Cardiovascular Surgery
- Pediatric Infectious Diseases
- Vascular Surgery
Background:
- Abdominal aortic aneurysms (AAAs) are uncommon in children, with infectious (mycotic) AAAs posing a significant rupture risk.
- Pediatric mycotic AAAs can rapidly expand, leading to aortic wall compromise and potential rupture.
- Early detection and intervention are critical for managing this rare but life-threatening condition in infants.
Observation:
- A 10-month-old infant, previously treated for hypoplastic left heart syndrome, developed methicillin-resistant Staphylococcus aureus bacteremia post-cardiac catheterization.
- An abdominal ultrasound, initially for renovascular hypertension, incidentally revealed a mycotic AAA.
- A prior CT scan showed normal aortic contours, indicating rapid aneurysm development.
Findings:
- The infant presented with a rapidly expanding mycotic AAA, a rare complication in pediatric patients.
- The mycotic AAA was diagnosed via abdominal ultrasound following a recent episode of bacteremia.
- Despite a recent normal CT scan, the aneurysm developed quickly, highlighting the aggressive nature of infectious AAAs.
Implications:
- This case underscores the importance of considering infectious etiologies for aortic abnormalities in pediatric patients, especially those with recent bacteremia.
- Prompt surgical intervention, such as open aneurysmorrhaphy with patch angioplasty, can effectively treat pediatric mycotic AAAs.
- Further research into the pathogenesis and optimal management strategies for pediatric mycotic AAAs is warranted.
Abstract:
Abdominal aortic aneurysms (AAAs) are a rare entity in the pediatric population. Children with mycotic (infectious) AAA in particular are at risk of life-threatening rupture due to their rapid expansion coupled with aortic wall thinning and deterioration. Here, we present the case of a 10-month-old infant with prior 2-staged repair for hypoplastic left heart syndrome that was incidentally discovered to have a mycotic AAA on abdominal ultrasound (US) for evaluation of renovascular hypertension. Before the time of evaluation with US, the infant had developed methicillin-resistant Staphylococcus aureus bacteremia 3 days after cardiac catheterization with percutaneous thoracic aortic balloon angioplasty. She had normal aortic contours on contrasted computed tomography scan of the abdomen approximately 2 weeks before the aforementioned US evaluation. This infant subsequently underwent open aneurysmorrhaphy with cryopreserved vein patch angioplasty with resolution of her aneurysmal segment.

