Primary Splenic Artery Aneurysm Diagnosed by EUS

Rebecca Lai, M.D.
Shawn Mallery, M.D
.

 

Keywords

Splenic artery aneurysm, EUS, pancreatic mass

Introduction

A 44-year-old male was referred for EUS evaluation of pancreatic mass.

Methods for EUS Capture

EUS examination was performed with the Pentax FG-32UA linear array echoendoscope at 5 MHz. Images were obtained using a Sony thermal printer and subsequently scanned and saved in .jpg format.

Case/Body

Figure 1

Figure 2

A 44-year-old male presented to an emergency room with a severe attack of epigastric pain associated with nausea and vomiting. He also gave a history of recurrent, episodic upper abdominal pain over the past ten years, occurring about twice a year. He had undergone an upper endoscopy in the past as work up for this abdominal pain, which was reportedly negative.

Past medical history was negative except for distant appendectomy and tonsillectomy. He was on no medications. Family history was non-contributory. He was a non-smoker and drank alcohol only occasionally.

Physical examination was unremarkable. The abdomen was non-tender and there was no bruit, palpable mass, or organomegaly.

Laboratory studies revealed a slightly elevated WBC at 13.1. Electrolytes and liver function tests were within normal limits. Serum amylase was elevated at 641 U/L (normal 30-110 U/L). An abdominal ultrasound was performed and revealed a 7 cm retroperitoneal inhomogeneous hypoechoic mass in the left upper quadrant. It was unclear whether this lesion was arising from the left adrenal or the pancreas. The patient subsequently had a CT of the abdomen that confirmed the presence of a homogeneous mass lesion with rim enhancement in the left upper quadrant, most likely arising from the pancreatic tail (Figures 1 and 2). No abnormal lymphadenopathy or ascites was noted. The patient was then referred for EUS evaluation and possible EUS-guided FNA of this mass lesion.

Figure 3

Figure 4

Linear array EUS identified a 72mm by 60 mm inhomogeneous hypoechoic round mass lesion with smooth margins in the region of the pancreatic tail (Figure 3). Along the anterior edge of the lesion was a 30mm by 25 mm anechoic structure which carried an arterial doppler signal (Figures 4, 5, and 6). This was demonstrated on EUS to be an aneurismal dilatation of the splenic artery as it could be followed continuously back to the celiac trunk medially and to the spleen laterally. A 7mm by 6 mm hyperechoic shadowing area of calcification was within the aneurysm (Figure 7). This mass lesion was displacing the splenic vein posteriorly without invading it. It was felt that the “mass” most likely represented a contained hematoma or a pseudoaneurysm, rather than a pancreatic mass. Thus, fine needle aspiration of the lesion was not performed.

The patient was referred for surgical resection of the splenic artery aneurysm. A distal pancreatectomy and splenectomy were necessary since the lesion could not be separated from the pancreatic tail. After further dissection, a defect 1cm in length was found in the splenic artery leading into the aneurysm. On final surgical pathology, the “mass” lesion was confirmed to be a large hematoma; the resection portion of the pancreas and the spleen were normal.

Figure 5

Figure 6

Figure 7

Discussion/Summary Statement

Primary splenic artery aneurysm is an uncommon vascular pathology, with incidence of 0.01% to 0.2% reported at autopsy series (1-3). It accounts for up to 60% of all visceral artery aneurysms (1,4). There is a female predominance, with the mean age of presentation at 52 years (1, 5-8). They are usually saccular, and the majority of them are located in the mid to distal splenic artery. (1, 6-8). The pathogenesis of splenic artery aneurysm is not fully understood. However, there are close associations with medial fibrodysplasia, multiple pregnancies, portal hypertension, liver transplant, and splenomegaly. Atherosclerosis and inflammation are often seen histologically; although they are most commonly secondary events resulting from primary degeneration of the media.

Most patients are asymptomatic, with aneurysm found incidentally on imaging studies. Up to 20% may present with epigastric or left upper quadrant abdominal pain (1, 9). Occasionally, the aneurysm can erode into an adjacent viscus or into the pancreatic duct and presents as gastrointestinal hemorrhage (3). Rupture of the aneurysm causes severe abdominal pain and hypovolemic shock. The initial rupture may be tamponaded within the lesser sac, with free intraperitoneal hemorrhage ensuing in minutes to hours. This double-rupture phenomenon allows valuable time for diagnosis and surgical intervention.

The reported risk of rupture varies from 3% to 10%, with a significant mortality rate of 36% after rupture. The risk of rupture is much higher during pregnancy and results in a maternal and fetal mortality rate of 70% and 95%, respectively (1-3, 6, 8-11).

Treatment is recommended for all patients with symptomatic or growing aneurysms and for all pregnant women and women of childbearing age who may subsequently become pregnant. Elective therapy should also be considered for good surgical candidates with large aneurysms (> 2cm) since they carry a higher risk of rupture (1, 2, 4-6, 8, 10, 12). Surgical treatment options include aneurysm resection or simple ligation. Depending on the location of the aneurysm, splenectomy and distal pancreatectomy may be necessary. Percutaneous transcatheter embolization, with success rate of over 80%, offers an attractive alternative to surgery, especially for patients with high surgical risk (6, 13, 14).

This case demonstrates how EUS could be used to safely and efficiently diagnose splenic artery aneurysm, which was subsequently confirmed at surgery.

References

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4. Rokke O, Sondenaa K, Amundsen SR, Larssen TB, Jensen D. Successful management of eleven splanchnic artery aneurysms. Eur J Surg 1997;163:411-417.

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9. Stanley JC, Fry WJ. Pathogenesis and clinical significance of splenic artery aneurysms. Surgery 1974;76:898-909.

10. Carr SC, Mahvi DM, Hoch JR, Archer CW, Turnipseed WD. Visceral artery aneurysm rupture. J Vasc Surg 2001;33:806-866.

11. Salo JA, Salmenkivi K, Tenhunen A, Kivilaakso EO. Rupture of splanchnic artery aneurysms. World J Surg 1986;10:123-127.

12. de Perrot M, Buhler L, Schneider PA, Mentha G, Morel P. Do aneurysms and pseudoaneurysms of the splenic artery require different surgical strategy? Hepato-gastroenterol 1999;46:2028-2032.

13. Salam TA, Lumsden AB, Martin LG, Smith RB. Nonoperative management of visceral aneurysms and pseudoaneuryms. Am J Surg 1992;164:215-219.

14. Reidy JF, Rowe PH, Ellis FG. Technical report: Splenic artery aneurysm embolisation - the preferred technique to surgery. Clin Radiol 1990;41:281-282.




Editorial Board:
Manoop S. Bhutani, M.D.
Galveston, TX
William R. Brugge, M.D.
Boston, MA
Peter R. McNally, D.O.
Denver, CO
Iqbal S. Sandhu, M.D.
Salt Lake City, UT
Thomas J. Savides, M.D.
San Diego, CA

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