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A large congenital and solitary intrahepatic arterioportal fistula in an old woman

By Zhen-Ya Lu, Jian-Yang Ao, Tian-An Jiang, Zhi-Yi Peng and Zhan-Kun Wang

Abstract

Arterioportal fistula (APF) is a rare cause of portal hypertension and may lead to death. APF can be congenital, post-traumatic, iatrogenic (transhepatic intervention or biopsy) or related to ruptured hepatic artery aneurysms. Congenital APF is a rare condition even in children. In this case report, we describe a 73-year-old woman diagnosed as APF by ultrasonography, computed tomography, and hepatic artery selective arteriography. The fistula was embolized twice but failed, and she still suffered from alimentary tract hemorrhage. Then, selective arteriography of the hepatic artery was performed again and venae coronaria ventriculi and short gastric vein were embolized. During the 2-year follow-up, the patient remained asymptomatic. We therefore argue that embolization of venae coronaria ventriculi and short gastric vein may be an effective treatment modality for intrahepatic APF with severe upper gastrointestinal bleeding

Topics: Case Report
Publisher: The WJG Press and Baishideng
OAI identifier: oai:pubmedcentral.nih.gov:2669954
Provided by: PubMed Central
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