We are reporting the rare case of splenic artery aneurysm of 4 cm of diameter presenting as a sub mucosal lesion on gastro-duodenal endoscopy. This aneurysm was treated by endovascular coil embolization and stent graft implantation. The procedure was uneventful. On day 1, the patient presented an acute severe epigastric pain and cardiovascular arrest. Abdominal computed tomography scan showed an active leak of the intravenous contrast dye in the peritoneum from the splenic aneurysm. We performed an emergent resection of the aneurysm, and peritoneal lavage. Postoperatively, hemorrhagic choc was refractory to large volumes replacement, and intravenous vaso-active drugs. On day 2, he presented massive hematochezia. We performed a total colectomy with splenectomy and cholecystectomy for ischemic colitis, with spleen and gallbladder infarction. Despite vaso-active drugs and aggressive treatment with Factor VIIa, the patient died after uncontrolled disseminated intravascular coagulation.

Splenic artery aneurysms (SAA) are a rare clinical entity that carry the risk of rupture and fatal hemorrhage (particularly those sized > 2 cm). SAA accounts for up to 60% of all splanchnic artery aneurysms and is the third most common intra-abdominal aneurysm following those of the aorta and the iliac arteries[1-7]. The diagnosis is often incidental on abdominal radiologic exams[7-12]. Symptomatic SAA (20%) may present with abdominal pain in the epigastrium or left upper quadrant. A more dramatic mode of presentation is spontaneous rupture of the aneurysm which is reported to occur in 2%-10% of patients as the initial presentation[1-12]. We report here a case of an 82-year-old man with SAA presenting as a sub mucosal lesion on upper gastro-duodenal endoscopy. We will discuss diagnosis tools of SAA, management and potential complications.

An 82-year-old male patient with a history of hypertension and smoking presented with vague epigastric pain. General physical examination was unremarkable. All labs were within normal limits. He underwent a diagnostic upper gastro-intestinal endoscopy and it showed a 5-cm firm non pulsating submucosal lesion in the fundus suggesting gastrointestinal stromal tumor (GIST) (Figure 1). Endoscopic ultrasound was then performed to characterize the sub mucosal lesion and to perform biopsies. It showed a round anechoic cystic mass measuring 3.5 cm in diameter, communicating with the splenic vessels and showing positive flow on Doppler ultrasound, suggesting a splenic artery aneurysm. Abdominal enhanced computed tomography (CT) scan and angioscan revealed a dilated and tortuous course of the splenic artery with a first saccular aneurysm of 20 mm of diameter behind the stomach lesser curvature, and a second saccular aneurysm of 43 mm of diameter projecting into the stomach (Figure 2). Via a femoral artery catheterization, the patient underwent an endovascular coil embolization and stent graft implantation to treat the aneurysms. The angiographic series taken after the procedure was satisfactory. The procedure was uneventful, and the patient was hemodynamically stable for the first few hours after endovascular repair. On day 1 post embolization, the patient presented an acute severe epigastric pain with rapid drop in arterial pressure and cardiovascular arrest. He was successfully resuscitated and intubated. An urgent abdominal enhancing CT scan revealed active extravasation of the intravenous contrast dye in the peritoneum from the splenic aneurysm confirming the diagnosis of ongoing peritoneal bleeding (Figure 3). We performed an emergent laparotomy with resection of the aneurysm, and peritoneal lavage. The patient is transferred to the intensive care unit. His hemorrhagic choc was refractory to large volumes of isotonic saline, multiple transfusions of packed red blood cells, fresh frozen plasma, platelets, and intravenous vaso-active drugs. On day 2, he presented massive hematochezia. A second laparotomy revealed an extensive ischemic colitis, with spleen and gallbladder infarction, as well as some hypo-perfused regions of the small intestine. We performed a total colectomy with splenectomy and cholecystectomy. Despite vaso-active drugs and aggressive treatment with Factor VIIa, the patient died after uncontrolled disseminated intravascular coagulation.

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Figure 1 Gastrodudenal endoscopy showing a 5-cm firm non pulsating sub mucosal lesion in the fundus.

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Figure 2 Abdominal enhanced computed tomography scan and angioscan showing a double aneurysm of splenic artery.

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Figure 3 Abdominal enhanced computed tomography scan showing a peritoneal leak of contrast material from splenic aneurysm.

SAA diagnosis is nearly always a fortuitous discovery by abdominal imaging (CT scan and ultrasound). In our case, the initial presentation was a sub-mucosal non pulsatile lesion detected on an upper gastro-duodenal endoscopy. At our knowledge, this type of presentation has not been described in the literature. Endoscopic ultrasound was initially done with the purpose of performing a fine needle aspiration of the lesion, thought to be a gastric sub-mucosal tumor as GIST. However, the positive Doppler flow detected shifted the diagnosis to a vascular lesion instead of a sub-mucosal tumor, and therefore fine needle aspiration was not performed. The prevalence of SAA is reported to be 0.1%-2%; however, the number of undetected SAAs may be much higher. The clinical presentation is nonspecific in most cases, and the diagnosis of SAA is often an incidental finding[5]. SAAs account for up to 75% of all visceral artery aneurysms and are more commonly reported in female patients than in male patients at a ratio of 4:1. Why SAAs predominate in women is not exactly clear, but a hormonal contribution has been postulated[13]. The pathophysiology of SAA is not fully understood, but local failure of the connective tissue of the arterial wall to maintain the integrity of the blood vessel could be playing a major role. Multiple risk factors have been listed including atherosclerosis, autoimmune diseases, collagen vascular diseases, pancreatitis, portal hypertension, traumatisms, fibromuscular dysplasia, female gender, and history of multiple pregnancies[11-16]. Nearly 70% of the SAA are saccular and situated at splenic hilum bifurcation[6]. Although the risk of rupture is low (nearly 2% of cases), ruptured SAA carry a high mortality rate, approaching 50%. Risk factors for rupture of the aneurysms include pregnancy, development of symptoms, expanding aneurysms, a diameter greater than 2 cm, portal hypertension, porto-caval shunt and liver transplantation[1,3,5,7,12]. Therefore, patients having one or more risk factor should undergo active treatment. Once the diagnosis of SAA is made, the essential goal of the physician remains to choose the adequate patient to treat as well as the right timing of any intervention. It is the general consensus that symptomatic SAA should be treated immediately, since rupture is associated with a high mortality rate. According to the guidelines, treatment is suggested for SAA with diameters > 2 cm or if the SAA is three times greater in diameter than the respective normal artery[5]. To treat symptoms and prevent complications, SAA repair is often required[4]. Various therapeutic options are available for patients with SAA, including conventional open surgery, endovascular treatment and, most recently, laparoscopic surgery[17-26]. Endovascular techniques (EV), including trans-catheter embolization and covered stent placement, can be used to treat most SAA regardless of the clinical presentation, etiology, or location of the aneurysm. If endovascular treatment is technically unavoidable, surgery should be considered given both good results and low morbidity. Open surgical treatment has traditionally been performed. The surgical procedures included ligation of the splenic artery, resection of the aneurysm and vascular reconstruction and/or bypass, and resection of the aneurysm with splenectomy. Complications rate of surgical treatment of non-ruptured aneurysm was 14.3%, and reached 25% in case with rupture[5]. The 30-d mortality rate of surgical treatment was 2.6% in non-ruptured aneurysm and 20.4% in rupture cases[13]. Recently, a per-cutaneous endovascular embolization procedure has become the first-line treatment for SAA. Packing of the aneurysmal sac with embolic agents (most commonly with coils, but also with detachable balloons and inert particles) and exclusion of the aneurysmal neck are the recommended techniques for treating splenic artery aneurysms. In our case, the patient had a 4 cm aneurysm and he was therefore treated with coil embolization and stent graft placement. Although trans-catheter arterial embolization (TAE) is associated with significantly lower morbidity and mortality than are surgical procedures, the possibility of organ ischemia or hemorrhagic events should not be underestimated. The success rate of TAE varies between 75% and 100%, with complication rate (aneurysm re-permeabilization, hemorrhage) ranging from 14% to 25%. The most common complications include acute pancreatitis, splenic infarction, splenic abscess, or intra-peritoneal hemorrhage. In case of an intra-peritoneal hemorrhage with hemodynamic instability, emergent laparotomy with resection of the aneurysm is the treatment of choice, with, however, high morbidity and mortality rate[5]. EV is the most cost-effective treatment for most patient groups with SAAs, independent of the sex and risk profile of the patient. EV is superior over OPEN in costs and effect for all age groups[4]. The results of meta-analysis show that EV of SAA has better short-term results than OPEN. However, OPEN is associated with fewer late complications and re-interventions during follow-up. The results of this meta-analysis show that SAAs > 2 cm should be treated, given the good short-term and long-term results. EV repair has the best outcomes and should be the treatment of choice if the splenic artery has a suitable anatomy for EV repair[13]. In our case, the patient had peritoneal hemorrhage at day 1 post embolization requiring emergent laparotomy. Despite aggressive treatment, the patient died after uncontrolled disseminated intravascular coagulation. In a large cohort evaluating prognostic factors associated with the clinical outcomes after TAE, multivariate analysis confirmed advanced patient age, post procedure thrombocytopenia, post procedure hydrothorax, and the need for a second intervention to be significant prognostic factors for overall 30-d morbidity[13]. In our case, the patient’s advanced age and the need for a second intervention after TAE were two prognostic factors associated with high short term morbidity and mortality.

In conclusion, SAA may be incidentally discovered on an upper gastro-duodenal endoscopy as a sub-mucosal lesion of the stomach. Caution must be made in order not to perform biopsies or fine needle aspiration to such lesions before checking for Doppler flow on endoscopic ultrasound. Treatment of choice for SAA of more than 2 cm of diameter is trans-catheter arterial embolization with a complication rate of around 20%. Intra-peritoneal hemorrhage after EV for SAA carry a high mortality rate despite emergent laparotomy and aggressive medical treatment.