Infected common iliac artery aneurysm repaired in an infant with cadaveric vein graft

Monahan, Denise; Neville, Holly L.; Saigal, Gaurav; Pérez, Eduardo A.; Sola, Juan E.

doi:10.1016/j.jpedsurg.2012.01.011

Cited by 5 publications

(4 citation statements)

References 6 publications

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“…Of patients undergoing LE reconstruction (n = 24), only one experienced postoperative graft thrombosis during follow-up. Although surgical repair was successful in our patient, future research questions include not only the use of conduits (cadaveric artery, cadaveric vein, synthetic graft) [ 14 ], but also the duration and risks of long-term anticoagulation/antiplatelet therapy required in children [ 11 ].…”

Section: Discussionmentioning

confidence: 99%

Peripheral vascular bypass with cadaveric arterial allograft in a toddler with femoral mycotic aneurysm

Huerta

Quinn

Restrepo

et al. 2023

Journal of Surgical Case Reports

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Mycotic aneurysms are exceedingly rare in the pediatric population. The optimal surgical treatment for children with this disease is unclear as aneurysm resection and vascular reconstruction are uncommonly performed in young children. We present a unique case of a 21-month-old child with a complex cardiac history who presented with limb ischemia and was discovered to have thrombosis of the common femoral and superficial femoral artery. Groin exploration revealed a left common femoral and superficial femoral artery mycotic aneurysm that was successfully repaired with excision of the mycotic aneurysm, external iliac to profunda femoral artery vascular bypass using cryopreserved arterial allograft and femoral vein reconstruction. This case demonstrates successful vascular reconstruction can be performed in a young child with an Aspergillus mycotic aneurysm using cadaveric arterial allograft.

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Section: Discussionmentioning

confidence: 99%

Peripheral vascular bypass with cadaveric arterial allograft in a toddler with femoral mycotic aneurysm

Huerta

Quinn

Restrepo

et al. 2023

Journal of Surgical Case Reports

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“…Nine months postoperatively, the graft remained patent. 4 In a final case report, one infant developed an infrarenal AAA and had her aneurysm resected and repaired with cryopreserved vein graft. Repair was patent at 1 year of follow-up.…”

Section: Discussionmentioning

confidence: 99%

Repair of a mycotic abdominal aortic aneurysm in a neonate using an everted jugular vein patch

Ahle

Cardella

Cleary

et al. 2017

Journal of Vascular Surgery Cases, Innovations and Techniques

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A 43-day-old boy presented with bacteremia after umbilical artery catheterization. Duplex ultrasound examination revealed a 1.1- × 1.6-cm mycotic infrarenal aortic aneurysm and an incidental asymptomatic occluded right common iliac artery. Resection and repair were completed by creating an everted, double-layered internal jugular vein patch. Screening ultrasound examination 10 months postoperatively demonstrated successful repair.

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“…Mycotic aneurysm is a disease that is particularly rare in children. Bacterial endocarditis used to be the most common cause in the past, but owing to the recent advances in antibiotics, it is now known to occur in association with neonatal umbilical artery catheterization [689]. Although the patient in this case had a history of undergoing inpatient pneumonia treatment twice, she did not have any special medical history during the neonatal period and no cardiac problem was found in the preoperative examinations.…”

Section: Discussionmentioning

confidence: 99%

Right iliac arterial aneurysm in a 4-year-old girl who does not have a right external iliac artery

Lee

Youn

et al. 2016

Ann Surg Treat Res

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Pediatric arterial aneurysm is rare disease. Among them, idiopathic-congenital arterial aneurysm is extremely rare. This is a case report of right common iliac artery idiopathic aneurysm with absence of right external iliac artery. A 4-year-old girl who had been complaining of intermittent abdominal pain since 2 years prior presented with a right lower abdominal mass that had been palpable since 6 months prior. Abdominal CT revealed a 5.2 cm × 4.5 cm × 5.1 cm, right-sided, partially thrombosed, saccular, iliac artery aneurysm. She underwent to operation, aneurismal resection. A pathological examination confirmed that it was a true aneurysm, considering that all layers of the vascular wall were stretched with no deficit. The patient was discharged 3 days after the surgery without any complication. Five months passed since the surgery, and the patient is doing well without any abdominal or leg pain.

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Infected common iliac artery aneurysm repaired in an infant with cadaveric vein graft

Cited by 5 publications

References 6 publications

Peripheral vascular bypass with cadaveric arterial allograft in a toddler with femoral mycotic aneurysm

Peripheral vascular bypass with cadaveric arterial allograft in a toddler with femoral mycotic aneurysm

Repair of a mycotic abdominal aortic aneurysm in a neonate using an everted jugular vein patch

Right iliac arterial aneurysm in a 4-year-old girl who does not have a right external iliac artery

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