A Giant Isolated External Iliac Artery Aneurysm Causing Hydronephrosis and Lower Extremity Weakness

1999 ◽  
Vol 33 (4) ◽  
pp. 435-438
Author(s):  
Simon K. H. Wong ◽  
W. S. Ho ◽  
William K. Loftus ◽  
Walter W. K. King
2019 ◽  
Vol 58 ◽  
pp. 386.e1-386.e3
Author(s):  
Ahmad Syed Hussain ◽  
Abdulhameed Aziz

2020 ◽  
Vol 26 (4) ◽  
pp. 216-219
Author(s):  
Shinsuke Nishimura ◽  
Takashi Murakami ◽  
Hiromichi Fujii ◽  
Yosuke Takahashi ◽  
Akimasa Morisaki ◽  
...  

Author(s):  
Caroline Mieko Tanaka ◽  
Marcelo Fernando Matielo ◽  
Edson Takamitsu Nakamura ◽  
Sergio Roberto Tiossi

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Nirmit Desai ◽  
Sagar Patel ◽  
Chinyere Nwosu ◽  
Lok Sung ◽  
Carl Tack ◽  
...  

We present a case of a patient with a failed pancreaticoduodenal allograft with exocrine enteric-drainage who developed catastrophic gastrointestinal (GI) hemorrhage. Over the course of a week, she presented with recurrent GI bleeds of obscure etiology. Multiple esophago-gastro-duodenoscopic (EGD) and colonoscopic evaluations failed to reveal the source of the hemorrhage. A capsule endoscopy and a technetium-labeled red blood cells (RBC) imaging study were similarly unrevealing for source of bleeding. She subsequently developed hemorrhagic shock requiring emergent superior mesenteric arteriography. Run off images revealed an external iliac artery aneurysm with fistulization into the jejunum. Coiled embolization was attempted but abandoned because of hemodynamic instability. Deployment of a covered endovascular stent into the right external iliac artery over the fistula site resulted in immediate hemodynamic stabilization. A high index of suspicion for arterioenteric fistulae is needed for diagnosis of this uncommon but eminently treatable form of GI hemorrhage in this patient population.


2003 ◽  
Vol 24 (1) ◽  
pp. 65-67 ◽  
Author(s):  
Mustafa Secil ◽  
Hasan Tahsin Sarisoy ◽  
Eyup Hazan ◽  
A.Yigit Goktay

Vascular ◽  
2007 ◽  
Vol 15 (2) ◽  
pp. 98-101 ◽  
Author(s):  
Peter Brant-Zawadzki ◽  
Daniel Kinikini ◽  
Larry W. Kraiss

Isolated mycotic common iliac artery aneurysms are rare, and as such, there is no consensus opinion on management. Traditional surgical options include resection with extra-anatomic bypass, placement of allograft or antibiotic treated synthetic graft, or autogenous vein reconstruction. We report the case of a 46-year-old, human immunodeficiency virus-positive male who presented with a recurrent pneumonia and new onset of right lower quadrant abdominal pain associated with right lower extremity swelling. computed tomographic scan revealed an isolated 9.5 cm right common iliac artery aneurysm with no evidence of rupture. Preoperative blood cultures grew out Streptococcus pneumoniae. Operative repair included aneurysm resection and reconstruction using an autogenous femoropopliteal vein interposition graft from the ipsilateral thigh. The patient had an uneventful recovery with resolution of his lower extremity swelling and a normal duplex exam at follow-up. Large mycotic common iliac artery aneurysms can be successfully treated with aneurysm resection and reconstruction using an autogenous femoropopliteal vein conduit. This technique obviates the need for extra-anatomic bypass or other forms of reconstruction using prosthetic material.


2020 ◽  
pp. 021849232097486
Author(s):  
Eijiro Yamashita ◽  
Taiji Watanabe ◽  
Keisuk Shuntoh ◽  
Kazunari Okawa ◽  
Akiyuki Takahashi

We present a patient with Stanford type A aortic dissection with malperfusion of the left kidney and lower extremity, and rupture of a common iliac artery aneurysm. After establishing lower extremity reperfusion using a percutaneous femorofemoral shunt in the emergency room, simultaneous open aortic arch repair and open abdominal aorta repair were performed. Our approach allowed concomitant repair of proximal dissection, limb ischemia, and iliac artery aneurysm rupture, all of which are critical predictors of mortality.


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