Open repair of an abdominal aortic and right common iliac artery aneurysm with idiopathic retroperitoneal fibrosis in a 19-month-old infant

Khalil Chamseddin; Antonio Solano; Melissa R. Keller; Michael C. Siah; Gerardo Gonzalez-Guardiola; Vivek Prakash; Michael Shih; M. Shadman Baig; Carlos H. Timaran; Melissa L. Kirkwood

doi:10.1016/j.jvscit.2024.101513

Open repair of an abdominal aortic and right common iliac artery aneurysm with idiopathic retroperitoneal fibrosis in a 19-month-old infant

Khalil Chamseddin, Antonio Solano, Melissa R. Keller, Michael C. Siah, Gerardo Gonzalez-Guardiola, Vivek Prakash, Michael Shih, M. Shadman Baig, Carlos H. Timaran, Melissa L. Kirkwood

Research output: Contribution to journal › Article › peer-review

Abstract

An abdominal aortic aneurysm (AAA) in children is a rare clinical condition, with idiopathic AAAs even more atypical. We report a case of a 19-month-old girl with incidental findings of an infrarenal AAA and right common iliac artery aneurysm during workup for heart failure. Extensive genetic testing was unremarkable for connective tissue disorders. An aortic bi-iliac artery bypass with a Dacron graft from the infrarenal aorta to the right external iliac artery and left common iliac artery was performed. The patient achieved complete recovery and only required one oral hypertensive medication at 30 days of follow-up. Wide patency of the graft was observed on the 3-month follow-up computed tomography angiogram.

Original language	English (US)
Article number	101513
Journal	Journal of Vascular Surgery Cases, Innovations and Techniques
Volume	10
Issue number	4
DOIs	https://doi.org/10.1016/j.jvscit.2024.101513
State	Published - Aug 2024

Keywords

Abdominal aortic aneurysm
Aortic disease
Congenital
Pediatric aneurysms
Pediatric vascular surgery
Surgical repair

ASJC Scopus subject areas

Surgery
Cardiology and Cardiovascular Medicine

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10.1016/j.jvscit.2024.101513

Cite this

Chamseddin, K., Solano, A., Keller, M. R., Siah, M. C., Gonzalez-Guardiola, G., Prakash, V., Shih, M., Baig, M. S., Timaran, C. H., & Kirkwood, M. L. (2024). Open repair of an abdominal aortic and right common iliac artery aneurysm with idiopathic retroperitoneal fibrosis in a 19-month-old infant. Journal of Vascular Surgery Cases, Innovations and Techniques, 10(4), Article 101513. https://doi.org/10.1016/j.jvscit.2024.101513

Open repair of an abdominal aortic and right common iliac artery aneurysm with idiopathic retroperitoneal fibrosis in a 19-month-old infant. / Chamseddin, Khalil; Solano, Antonio; Keller, Melissa R. et al.
In: Journal of Vascular Surgery Cases, Innovations and Techniques, Vol. 10, No. 4, 101513, 08.2024.

Research output: Contribution to journal › Article › peer-review

Chamseddin, K, Solano, A, Keller, MR, Siah, MC , Gonzalez-Guardiola, G, Prakash, V, Shih, M , Baig, MS , Timaran, CH & Kirkwood, ML 2024, 'Open repair of an abdominal aortic and right common iliac artery aneurysm with idiopathic retroperitoneal fibrosis in a 19-month-old infant', Journal of Vascular Surgery Cases, Innovations and Techniques, vol. 10, no. 4, 101513. https://doi.org/10.1016/j.jvscit.2024.101513

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title = "Open repair of an abdominal aortic and right common iliac artery aneurysm with idiopathic retroperitoneal fibrosis in a 19-month-old infant",

abstract = "An abdominal aortic aneurysm (AAA) in children is a rare clinical condition, with idiopathic AAAs even more atypical. We report a case of a 19-month-old girl with incidental findings of an infrarenal AAA and right common iliac artery aneurysm during workup for heart failure. Extensive genetic testing was unremarkable for connective tissue disorders. An aortic bi-iliac artery bypass with a Dacron graft from the infrarenal aorta to the right external iliac artery and left common iliac artery was performed. The patient achieved complete recovery and only required one oral hypertensive medication at 30 days of follow-up. Wide patency of the graft was observed on the 3-month follow-up computed tomography angiogram.",

keywords = "Abdominal aortic aneurysm, Aortic disease, Congenital, Pediatric aneurysms, Pediatric vascular surgery, Surgical repair",

author = "Khalil Chamseddin and Antonio Solano and Keller, {Melissa R.} and Siah, {Michael C.} and Gerardo Gonzalez-Guardiola and Vivek Prakash and Michael Shih and Baig, {M. Shadman} and Timaran, {Carlos H.} and Kirkwood, {Melissa L.}",

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AU - Chamseddin, Khalil

AU - Solano, Antonio

AU - Keller, Melissa R.

AU - Siah, Michael C.

AU - Gonzalez-Guardiola, Gerardo

AU - Prakash, Vivek

AU - Shih, Michael

AU - Baig, M. Shadman

AU - Timaran, Carlos H.

AU - Kirkwood, Melissa L.

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N2 - An abdominal aortic aneurysm (AAA) in children is a rare clinical condition, with idiopathic AAAs even more atypical. We report a case of a 19-month-old girl with incidental findings of an infrarenal AAA and right common iliac artery aneurysm during workup for heart failure. Extensive genetic testing was unremarkable for connective tissue disorders. An aortic bi-iliac artery bypass with a Dacron graft from the infrarenal aorta to the right external iliac artery and left common iliac artery was performed. The patient achieved complete recovery and only required one oral hypertensive medication at 30 days of follow-up. Wide patency of the graft was observed on the 3-month follow-up computed tomography angiogram.

AB - An abdominal aortic aneurysm (AAA) in children is a rare clinical condition, with idiopathic AAAs even more atypical. We report a case of a 19-month-old girl with incidental findings of an infrarenal AAA and right common iliac artery aneurysm during workup for heart failure. Extensive genetic testing was unremarkable for connective tissue disorders. An aortic bi-iliac artery bypass with a Dacron graft from the infrarenal aorta to the right external iliac artery and left common iliac artery was performed. The patient achieved complete recovery and only required one oral hypertensive medication at 30 days of follow-up. Wide patency of the graft was observed on the 3-month follow-up computed tomography angiogram.

KW - Abdominal aortic aneurysm

KW - Aortic disease

KW - Congenital

KW - Pediatric aneurysms

KW - Pediatric vascular surgery

KW - Surgical repair

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Open repair of an abdominal aortic and right common iliac artery aneurysm with idiopathic retroperitoneal fibrosis in a 19-month-old infant

Abstract

Keywords

ASJC Scopus subject areas

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