Spontaneous rupture of hepatic artery aneurysm associated with polyarteritis nodosa

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Abstract

Polyarteritis nodosa (PAN) is a vasculitis, which often involves small and medium sized visceral arteries. This condition may result in multifocal aneurismal formation and end-organ damage. Uncommonly, PAN may present with rupture of hepatic artery aneurysms. Here, we report a rare case of a ruptured intrahepatic aneurysm associated with PAN. A 79-year-old woman presenting with abdominal pain had CTscan of the abdomen, which revealed hematoma in the right hepatic lobe. Visceral angiogram confirmed pseudo-aneurysm of a right hepatic arterial branch, and this was managed with endovascular coil embolization. The diagnosis of PAN was made and corticosteroid therapy was initiated. We also performed a literature review to define this condition's demographics, clinical presentations, and appropriate management. The review revealed 17 published cases of ruptured PAN-related intrahepatic aneurysms. We conclude that unexplained findings of visceral arterial aneurysms should prompt investigations for vasculitis as the etiology.

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Parent, B. A., Cho, S. W., Buck, D. G., Nalesnik, M. A., & Gamblin, T. C. (2010). Spontaneous rupture of hepatic artery aneurysm associated with polyarteritis nodosa. American Surgeon, 76(12), 1416–1419. https://doi.org/10.1177/000313481007601230

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