Abstract
Congenital abdominal aortic aneurysms are rare but have chronic and life-threatening sequelae including hypertension, thromboses, and death. A fetal ultrasound at 27 weeks' gestation diagnosed a giant abdominal aortic aneurysm. The patient delivered at another tertiary care center where pediatric cardiovascular surgery care was available. Her term 3096-g female infant developed hypertension, biventricular hypertrophy, and right kidney ischemia. She underwent surgical repair at 2 months of life but subsequently lost all residual renal function and was not a candidate for dialysis. Support was withdrawn and she expired. Although isolated fetal AAA is rare, prenatal diagnosis is feasible and facilitates early referral for multi-disciplinary postnatal care. Outcome depends on the size and location of the aneurysm as well as on perioperative complications.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 61-63 |
| Number of pages | 3 |
| Journal | Case Reports in Perinatal Medicine |
| Volume | 3 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jun 1 2014 |
Keywords
- 2D and 3D ultrasound
- Abdominal aortic aneurysm
- Color Doppler
- Prenatal diagnosis
ASJC Scopus subject areas
- Obstetrics and Gynecology
- Pediatrics, Perinatology, and Child Health
- Embryology
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