Case Reports in Medicine

Case Reports in Medicine / 2010 / Article

Case Report | Open Access

Volume 2010 |Article ID 287034 |

Lidia Santarpia, Massimiliano Creta, Umberto Marcello Bracale, Roberto Ciccarelli, Fabrizio Pasanisi, Franco Contaldo, Ciro Imbimbo, "Ureteroiliac Artery Fistula in a Young Woman with Short Bowel Syndrome for Radiation Enteritis", Case Reports in Medicine, vol. 2010, Article ID 287034, 3 pages, 2010.

Ureteroiliac Artery Fistula in a Young Woman with Short Bowel Syndrome for Radiation Enteritis

Academic Editor: Tomas A. Salerno
Received31 Jan 2010
Accepted23 Feb 2010
Published14 Mar 2010


Ureteral-iliac artery fistula is a rare and potentially life-threatening complication, typically occurring after radiation therapy in already surgically treated cancer patients. This case report describes the diagnostic challenges and the successful management, with the positioning of an intra-arterial prosthesis, of a fistula between the internal iliac artery and the left ureter presenting as massive hematuria in a young woman with history of total colectomy and pelvic radiotherapy for rectal cancer and subsequent wide ileal resections and bilateral ureteral stent positioning for radiation enteritis. Ureteroiliac artery fistulas require a prompt diagnosis and intervention, to avoid life threatening clinical events.

1. Case Report

In October 2008, a 29-year-old woman was admitted as emergency to the Department of Urology with massive hematuria and left hip colic pain.

In 2004 she underwent a total colectomy followed by adjuvant systemic chemotherapy and radiotherapy for rectal carcinoma arising on colon familial adenomatous poliposis. Between 2005 and 2007 she developed several intestinal occlusions secondary to radiation enteritis requiring four laparotomies followed by resections of aderential bridles and wide ileal segments. Finally a cutaneous ileostomy was confectioned and daily Parenteral Nutrition prescribed. In 2006 intestinal continuity was restored. In February 2008, a Computed Tomography (CT) scan showed a bilateral hydroureteronephrosis due to a nonhomogeneous mass completely filling the pelvic region and bilateral ureteral stents were placed in order to preserve renal function. In April 2008, an exploratory laparotomy was performed which identified an abscessual collection due to the dehiscence of ileoanal anastomosis: the collection was drained and a new cutaneous ileostomy confectioned. In July and in September 2008, the right and left ureteral stents were, respectively, replaced due to infection.

On admission, a three-way catheter with a bladder washing was placed. A CT scan with contrast medium (CM-CT) showed bladder tamponade (Figure 1) and blood clots in both renal pelvis: the site of bleeding could not be identified. A cystoscopy was performed, bladder clots were evacuated, and bladder bleeding was excluded. A subsequent abdominal CM-CT scan showed left ureteral stent dislocation in the renal parenchyma with a small superior renal pole infarction. A selective left renal arteriography did not reveale primary renal bleeding. During the attempt of the left ureteral stent removal, the patient had a massive ureteral haemorrhage and collapsed. She was promptly revived with plasma expanders and blood transfusions. A ureteral catheter was positioned with a continuous bladder washing. During the ensuing week, she had intermittent but self-limiting bleeding from the left ureteral catheter. A second arteriography was unremarkable; a left superior renal pole selective artery embolization was performed but it failed to control bleeding. After one-week stabilization, a further attempt to remove the ureteral catheter was done followed by a massive ureteral bleeding. After further counseling with general and vascular surgeons for an exploratory laparotomy, a third CM-CT integrated by colour Doppler ultrasound examination was performed which identified an hydronephrotic, nonfunctioning left kidney with a left hydroureter until the cross with left common iliac artery. A pseudoaneurysm of the right proximal common iliac artery adjacent to the left ureter was detected, and an ureteroarterial fistula was suspected (Figures 2 and 3). The patient underwent to the placement of a covered, self-expandable vascular stent with angioplasty balloon without any further urinary bleeding up to now, that is, 4 months after the intervention. Moreover, a full recovery of left renal function was obtained.

2. Discussion

Arterioureteral fistulae occur very rarely, often difficult to indentify, like the one described in this case report, and could be associated with a high mortality rate [1] mainly due to delay in diagnosis and treatment. Radiation therapy, previous vascular surgery, prolonged ureteral stenting, prior pelvic surgery, vascular pathology, and endoureteral procedure all are conditions that can predispose to fistula formation between and artery and the ureter [2]. The patient described in this report had chronic indwelling stents and previous radiation therapy to the pelvis. The constant pulsation of the iliac artery is transmitted to a very compromised ureter (hydroureteronephrosis, infection, pelvic surgery, hypotension, and finally left hydroureter) resulting a pressure necrosis, most likely where the ureter crosses the iliac artery [3, 4]. To avoid fistula formation in debilitated patients treated previously with radiation and surgery, the use of small and soft stents is recommended [5].

The treatment of these fistulae has also changed overtime, from open surgery to stent-graft repair, which is less invasive than the open approach [46].


  1. D. B. Kerns, M. D. Darcy, D. S. Baumann, and B. T. Allen, “Autologous vein-covered stent for the endovascular management of an iliac artery-ureteral fistula: case report and review of the literature,” Journal of Vascular Surgery, vol. 24, no. 4, pp. 680–686, 1996. View at: Publisher Site | Google Scholar
  2. D. Bergqvist, H. Pärsson, and A. Sherif, “Arterio-ureteral fistula—a systematic review,” European Journal of Vascular and Endovascular Surgery, vol. 22, no. 3, pp. 191–196, 2001. View at: Publisher Site | Google Scholar
  3. D. C. Madoff, S. Gupta, B. D. Toombs et al., “Arterioureteral fistulas: a clinical, diagnostic, and therapeutic dilemma,” American Journal of Roentgenology, vol. 182, no. 5, pp. 1241–1250, 2004. View at: Google Scholar
  4. P. F. Escobar, J. L. Howard, J. Kelly et al., “Ureteroarterial fistulas after radical pelvic surgery: pathogenesis, diagnosis, and therapeutic modalities,” International Journal of Gynecological Cancer, vol. 18, no. 4, pp. 862–867, 2008. View at: Publisher Site | Google Scholar
  5. R. C. van den Bergh, F. L. Moll, J. P. de Vries, K. K. Yeung, and T. M. Lock, “Arterio-ureteral fistula: 11 new cases of a wolf in sheep's clothing,” The Journal of Urology, vol. 179, no. 2, pp. 578–581, 2008. View at: Google Scholar
  6. A. E. Krambeck, D. S. DiMarco, M. T. Gettman, and J. W. Segura, “Ureteroiliac artery fistula: diagnosis and treatment algorithm,” Urology, vol. 66, no. 5, pp. 990–994, 2005. View at: Publisher Site | Google Scholar

Copyright © 2010 Lidia Santarpia et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

Article of the Year Award: Outstanding research contributions of 2020, as selected by our Chief Editors. Read the winning articles.