Abstract
VAAs are a rare entity; however, aneurysm rupture, which is the catastrophic complication, may lead to a mortality rate up to 90 % according to the location of the aneurysm. Timely diagnosis of VAA is the most important, and individualized treatment is tailored based on the symptoms and signs, size, location, anatomy, and etiology of the aneurysm, as well as patient’s surgical risk. Currently, there is no consensus regarding treatment guidelines. Asymptomatic patients with VAA < 2.0 cm in diameter can be observed with close imaging follow-up which includes DUS, CTA, or MRA. In general, interventions are indicated in symptomatic or ruptured VAAs, pseudoaneurysms, asymptomatic patients with aneurysm > 2.0 cm, and aneurysm with rapid increase in size ≥ 0.5 cm/year. Besides, due to the high risk of rupture, regardless of size or symptom, interventions are also recommended in female patient of childbearing age or pregnant and orthotopic liver transplant recipient who harbors an SAA patient with visceral branch aneurysms. Surgical repair includes excision of the VAA with or without revascularization or organ resection; endovascular therapy includes embolization and placement of covered stents. Regardless of the procedure performed, revascularization must be considered when there is inadequate or no collateral flow to maintain end-organ perfusion. Long-term results of open repair of VAAs are durable; endovascular treatment, as a promising alternative to open surgery especially in anatomically suitable and high risk patients, provides good short-term results; however, its long-term results are not yet well known. Follow-up data from randomized controlled trials and prospective studies are required to justify the treatment strategy for VAAs.
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Huang, Y., de Souza, L.R., Oderich, G.S., Stone, W.M. (2015). Clinical Presentation, Etiology, Diagnostic Considerations, Treatment, and Results. In: Oderich, G. (eds) Mesenteric Vascular Disease. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-1847-8_34
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