AJR AJR-based Continuing Ed for Technologists
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Owens, C. A.
Right arrow Articles by Benedetti, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Owens, C. A.
Right arrow Articles by Benedetti, E.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
AJR 2002; 179:1327-1329
© American Roentgen Ray Society


Technical Innovation

Coil Embolization of a Wide-Neck Splenic Artery Aneurysm Using a Remodeling Technique

Charles A. Owens1, Babak Yaghmai1, Victor Aletich1 and Enrico Benedetti2

1 Department of Radiology, M/C 931, University of Illinois Medical Center at Chicago, 1740 W. Taylor St., Chicago, IL 60612.
2 Department of Transplant Surgery, University of Illinois Medical Center at Chicago, Chicago, IL 60612.

Received March 4, 2002; accepted after revision April 9, 2002.

 
Address correspondence to C. A. Owens.


Introduction
Top
Introduction
Case Report
Discussion
References
 
Splenic artery aneurysms are rare but important vascular lesions that occur in up to 10% of patients with cirrhosis and portal hypertension [1]. Most splenic artery aneurysms that are found in patients awaiting liver transplantation are asymptomatic and are incidentally discovered during routine screening examinations. The important association between splenic artery aneurysms and liver transplant recipients is the risk of rupture and associated high mortality after surgery [2].

We describe the case of a large hilar splenic artery aneurysm complicated by a wide aneurysmal neck found in a patient awaiting a liver transplantation. To preserve splenic function and reduce the risk of aneurysmal rupture, we used a remodeling technique to isolate and embolize the aneurysm with Guglielmi detachable coils (Target Therapeutics, Fremont, CA).


Case Report
Top
Introduction
Case Report
Discussion
References
 
A 59-year-old man with end-stage liver disease associated with ethanol abuse and hepatitis C was referred for preoperative arterial portography after MR imaging of the portal vein system revealed thrombosis of the main portal vein. Splenic artery portography was performed to better define the remaining portal vein anatomy. During arteriography, a 20-mm saccular aneurysm was identified in the splenic hilum (Fig. 1A). The aneurysm was not identified on previous MR imaging and CT of the upper abdomen. After discussion with the transplantation service, we rescheduled the patient for selective transcatheter embolization of the splenic aneurysm.



View larger version (140K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 1A. 59-year-old man with end-stage liver disease. Splenic artery angiogram obtained before embolization shows large wide-neck aneurysm near splenic artery bifurcation. Note associated smaller branch artery (arrows) extending from base of aneurysm occluded during embolotherapy.

 

Using a right transfemoral artery approach, we placed a 5-French catheter (Cobra 2; Cook, Bloomington, IN) through a 5-French introducer sheath (Cordis, Miami, FL) and positioned the catheter in the main splenic artery. Splenic arteriograms were obtained with the patient in various positions. The arteriograms identified a small branch artery emerging from the base of the aneurysm (Fig. 1A). Computer-assisted measurements of the main splenic artery, branch artery, and aneurysm were obtained using a standard software package (Neurostar; Seimens, Erlangen, Germany) found in our angiography suite. An attempt was made to occlude the aneurysm using appropriately sized Guglielmi detachable coils deployed through a coaxially placed 3-French Tracker-18 catheter with double markers (Target Therapeutics). After coils were deposited in the small branch artery extending from the base of the aneurysm, we abandoned further attempts to embolize the aneurysm when additional Guglielmi detachable coils protruded into the lumen of the main branch artery.

The 5-French catheter and the sheath were replaced with a 90-cm-long, 8-French guiding catheter (Cordis) that was positioned in the main splenic artery. A 9-French double rotating Y connector with an adjustable valve was attached to the end of the guiding catheter to allow side-by-side placement of a turbo Tracker-18 catheter and a nondetachable silicone balloon microcatheter (Endeavor; Target Therapeutics). A 5000-U bolus of heparin was administered to the patient to prevent thrombosis during temporary arterial occlusion. The Tracker-18 catheter was placed in the aneurysm, after which the nondetachable silicone balloon microcatheter was positioned across the neck of the aneurysm and inflated with diluted contrast material, causing temporary occlusion of the aneurysmal neck. With the neck of the aneurysm protected, we deposited Guglielmi detachable coils in the lumen of the aneurysm (Fig. 1B). Road-mapping was used during deployment. Before detachment of each coil, the balloon was deflated to test the stability of the coil in the aneurysm. Whenever the coil protruded across the neck of the aneurysm, the coil was retrieved and another deployment was attempted using either the Tracker-18 catheter placed in a different position in the aneurysm or a smaller coil.



View larger version (141K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 1B. 59-year-old man with end-stage liver disease. Radiograph shows nondetachable microballoon inflated across neck of aneurysm as Guglielmi detachable coil (Target Therapeutics, Fremont, CA) (arrows) is deposited in aneurysmal lumen.

 

Complete occlusion of the aneurysm was achieved after 12 Guglielmi detachable coils of sequentially decreasing lengths (10-30 cm) and helical diameters (4-16 mm) were deployed. Repeated arteriography was performed during and at completion of embolization, confirming patency of the major branch artery and occlusion of the densely packed aneurysm (Fig. 1C).



View larger version (133K):
[in this window]
[in a new window]
[as a PowerPoint slide]
 
Fig. 1C. 59-year-old man with end-stage liver disease. Angiogram obtained after embolization shows occlusion of aneurysm after deployment of 12 Guglielmi detachable coils.

 

The remainder of the patient's hospitalization was uneventful and without clinical or laboratory evidence of splenic infarction. Three weeks after embolization, the patient underwent a successful liver transplantation. Intraoperative examination of the spleen revealed a normal splenic capsule and no gross evidence of splenic infarction. The patient's perioperative and postoperative courses were unremarkable. At 12 months after the liver transplantation, the patient showed no signs or symptoms of splenic infarction or aneurysmal rupture.


Discussion
Top
Introduction
Case Report
Discussion
References
 
Eight percent to 10% of patients with cirrhosis and portal hypertension have splenic artery aneurysms, a 10-fold increase compared with the general population [1, 3]. Although the pathogenesis of splenic artery aneurysms in patients with cirrhosis is not fully understood, portal hypertension and the hyperdynamic flow associated with cirrhosis appear to be predisposing factors [4]. In addition, hormonal changes similar to those seen during pregnancy have been implicated in contributing to increased weakening of vessel walls and aneurysmal rupture [4]. These hormonal changes are the result of decreased catabolism due to chronic liver damage [4].

Rupture of splenic artery aneurysms after liver transplantation has been well documented [1, 2, 4]. The reduction of portal vein resistance after liver transplantation increases splenic artery blood flow and thereby the risk of aneurysmal rupture. Gitlin et al. [5] showed a 44% increase in splenic blood flow after surgical portocaval shunts were placed. This increase was seen despite a decrease in splenic size, and the increase remained unchanged after several years of follow-up (1-14 years). A similar increase in splenic blood flow after liver transplantation may account for the reported postoperative rupture of splenic artery aneurysms and the appearance of new aneurysms after transplantion surgery [1, 2, 4]. Treatment of these aneurysms by ligation of the splenic artery has been recommended at the time of liver transplantation, when the size of the aneurysm is greater than 10 mm in diameter and is isolated to the main splenic artery [1, 2, 4]. As in our patient, hilar aneurysms account for 87% of splenic artery aneurysms found in transplantation patients and require splenectomy if they are not treated by endovascular means [4].

Our decision to embolize the hilar aneurysm was complicated by the presence of a wide aneurysmal neck. The use of the remodeling technique to treat wide-neck or poorly shaped aneurysms was first described by Moret et al. [6]. This technique has been shown to be highly effective in the endovascular treatment of intracranial aneurysms [7]. By temporally occluding the neck of the aneurysm during deployment of the Guglielmi detachable coil, the operator can then create a basket of coils in the aneurysm. Filling of the basket is achieved by successive deployment of Guglielmi detachable coils with a shorter length and smaller helical size until the aneurysm is occluded. The balloon occlusion catheter prevents migration of the coils across the neck of the aneurysm by providing a temporary barricade during deployment.

Our choice to selectively embolize the aneurysm during temporary occlusion of the aneurysmal neck proved to be effective at preserving the patency of the adjacent branch artery and minimizing the risk of splenic infarction. Alternative surgical therapies to treat the aneurysm could result in a loss of time and additional blood loss during the planned transplantation surgery. A splenectomy would pose the additional risk of severe infection to an already immunosuppressed liver recipient [8].

Further studies are needed to determine the proper workup and treatment of asymptomatic splenic artery aneurysms in patients who plan to undergo a liver transplantation or portosystemic shunt procedure. Researchers have shown the effectiveness of the remodeling technique in the treatment of wide-neck intracranial aneurysms [7]. We anticipate that the use of this technique in the treatment of visceral aneurysms, as in our patient, will be equally successful.


References
Top
Introduction
Case Report
Discussion
References
 

  1. Ayalon A, Wiesner RH, Perkins JD, Tominaga S, Hayes DH, Krom AF. Splenic artery aneurysms in liver transplant patients. Transplantation 1988;45:386 -389[Medline]
  2. Bronsther O, Merhav H, Van Thiel D, Starzl TE. Splenic artery aneurysms occurring in liver transplant recipients. Transplantation 1991;52:723 -724[Medline]
  3. Stanley JC, Fry WJ. Pathogenesis and clinical significance of splenic artery aneurysms. Surgery 1974;76:898 -909[Medline]
  4. Kobori L, van der Kolk MJ, de Jong KP, et al. Splenic artery aneurysms in liver transplant patients. J Hepatol 1997;27:890 -893[Medline]
  5. Gitlin N, Grahame GR, Kreel L, Williams HS, Sherlock S. Splenic blood flow and resistance in patients with cirrhosis before and after portocaval anastomoses. Gastroenterology 1970;59:208 -213[Medline]
  6. Moret J, Pierot L, Boulin A, et al. "Remodelling" of the arterial wall of the parent vessel in the endovascular treatment of intracranial aneurysms. (abstr) Neuroradiology 1994;36[suppl 1]:83S
  7. Moret J, Cognard C, Weill A, Castaings L, Rey A. Reconstruction technic in the treatment of wideneck intracranial aneurysms: long-term angiographic and clinical results—apropos of 56 cases [in French]. J Neuroradiol 1997;24:30 -44[Medline]
  8. Schwartz, PE, Sterioff S, Mucha LJ III, Offord KP. Postsplenectomy sepsis and mortality in adults. JAMA 1982;248:2279 -2283[Abstract]

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
ANGIOLOGYHome page
M. Vlychou, C. Kokkinis, S. Stathopoulou, C. Tsilikas, O. Lazoura, A. Petinelli, P. Papadaki, and I. Fezoulidis
Imaging Investigation of a Giant Splenic Artery Aneurysm
Angiology, August 1, 2008; 59(4): 503 - 506.
[Abstract] [PDF]


This Article
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Owens, C. A.
Right arrow Articles by Benedetti, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Owens, C. A.
Right arrow Articles by Benedetti, E.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS