Abstract
Acutely aggravated dissecting flap and consequent occlusion of the superior mesenteric artery (SMA) by simple contrast passage during initial angiography for percutaneous stent placement is a uncommon event, which usually is not reported. After analysis of many factors that underlie development of such complications, we present herein one case of successful treatment of isolated SMA dissection and its complications with favorable outcomes during 25 months follow-up after percutaneous stent placement.
Keywords: Superior mesenteric artery dissection, percutaneous stent
INTRODUCTION
Very few cases of acute mesenteric ischemia (AMI) caused by spontaneous dissection of the superior mesenteric artery (SMA) have been reported. There are several therapeutic options including conservative management, surgical repair, implantation, and more recently, endovascular treatment.
We report a very rare, contrast injection-induced, acute aggravation of a preexisting dissecting flap of a spontaneous SMA dissection during endovascular treatment.
CASE REPORT
A 43-year-old man with a previous history of hypertension complained of sudden severe epigastric pain that began 6 hours before admission and rapidly progressed to more severe diffuse abdominal pain. Physical examination was consistent with suspected surgical abdomen. The laboratory data showed no significant abnormalities. Abdominal computed tomography (CT) showed a focal dissecting flap in the proximal SMA (white arrow) with a severely narrowed true lumen (Fig. 1). The SMA angiogram showed a focal dissection flap 2 cm distally from the origin (arrow) with a combined dissecting aneurysm (arrowheads) (Fig. 2A). Immediately after contrast injection during SMA angiography, the dissecting flap propagated acutely and rapidly (arrows), and a large amount of thrombus migrated to the entire distal trunk of the SMA, the iliocolic, and jejunal branches (arrowheads), leaving the SMA main trunk nearly occluded (Fig. 2B).
After cannulation of the SMA main trunk with a 2.4F microcatheter, a total of 500,000 I.U urokinase were continuously infused through angiographic catheter and microcatheter separately during 15 minutes, and aspiration embolectomy was performed with a 7F aspiration catheter. After removal of most of the thrombus within the SMA main trunk, a 7 mm×6 cm self expandable stent (Protégé; Micro Therapeutics, ev3, Irvine, CA, USA) was deployed over the dissection flap at the proximal SMA (white arrows), while jejunal branches remained occluded due to distally migrated thrombus (white arrowheads) (Fig. 3A). Completion angiography showed a completely excluded dissecting flap in the proximal SMA and complete recanalization of the SMA and its branches (Fig. 3B). The patient experienced complete improvement symptom of the immediately after the procedure and remained asymptomatic during 25 months of follow-up.
DISCUSSION
Embolic or thrombotic occlusion of the SMA frequently occurs, often leading to AMI.1-3 While isolated spontaneous dissection of the SMA is an uncommon cause of AMI, the number of case reports of the latter presentation has increased in recent years.4
The most common locations for dissecting flaps of the SMA are 1 to 6 cm from the os of the SMA (mean 2.7 cm), often accompanied by aneurismal change of the proximal SMA. Infrequently, however, dissection flaps are present without aneurismal change of the proximal SMA.5,6
Recently, multidetector-row computed tomography has been found to facilitate accurate demonstration of an obstruction of the SMA and changes in ischemic bowel segments, and it is found to be helpful in detecting dissecting flaps and demonstrating combined intraluminal thrombus or aneurismal change.7,8 The dissecting flap is not always visualized by CT scanning, therefore, if the occlusion of SMA is visualized by CT, then one can consider the SMA dissection as the possible cause of AMI. The present case showed a definite dissecting flap and intramural hematoma in the proximal SMA on initial CT.
Surgical treatment was commonly used for SMA dissection in the past, however, medical therapy or spontaneous resolution of SMA dissection has rarely been reported.4,5 Since Leung, et al. first reported on the use of percutaneous stent placement for the treatment of SMA dissection, the use of percutaneous endovascular approach to treat isolated SMA dissections has increased.9 In most cases, self-expandable stents with diameters up to 10 mm and overall lengths up to 10 cm have been used, although the evidence-based data to reveal the selection of the most ideal stent types for such specific cases are laking. Most authors favor a self-expandable stent because of its radial strength, conformability and sufficient length.10
Despite its growing popularity, there are several concerns about percutaneous stent placement for the treatment of SMA dissection; including vessel rupture, thrombotic stent occlusion, infection, stenosis of the native vessel around the stent, and lack of long-term follow-up data. However, endovascular therapy shows good results and it is an attractive option to address SMA dissection, as illustrated in this report as well as other series.11,12
There are a few reports on contrast passage-induced/aggravated dissection during angiography for stent placement.13-17 In our case, the dissecting flap could suddenly be aggravated and extended by simple contrast injection during angiography.
The possible cause was that the passage of high pressure and concentration contrast material through the severely narrowed true lumen damaged and ruptured the dissecting flaps, and that the false lumen thrombus propagated into the true lumen.
There was no possibility of deep engagement of the angiographic catheter tip into the false lumen, because we identified the catheter tip into the true lumen by test contrast injection before angiography. Furthermore, initial CT revealed that the false lumen on proximal SMA was occupied with intramural hematoma.
We can suspect that the highly risky underlying condition led to the unpredictable complications in our case, including the fast developing dissecting flap or visualized unstable flap during contrast injection; the unstable intraluminal thrombus around the dissection flap and severely narrowed true lumen around the dissection flap.
We can prevent this complication during angiography by using smaller volumes of contrast and by insertion of a safety guidewire into the true lumen before angiography.
In conclusion, an increasing number of studies suggest the efficacy and safety of percutaneous stent placement for the treatment of isolated SMA dissection. However, high-risk conditions for propagation of dissecting flap simply by contrast passage during initial angiography need to be taken into consideration.
Footnotes
The authors have no financial conflicts of interest.
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