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[A case of refractory ascites due to splenic arteriovenous fistula appeared during the course of observation and cured by embolization therapy].

作者信息

Hosokawa Takanori, Uraushihara Koji, Kawaguchi Atsushi, Kojima Shigeru, Sakurai Yuki, Suzuki Shoko, Kobayashi Masayuki, Ohno Kazumasa, Kikuchi Ohki, Takeda Yuichi

机构信息

Department of Gastroenterology, Showa General Hospital.

Department of Endoscopy, Showa General Hospital.

出版信息

Nihon Shokakibyo Gakkai Zasshi. 2022;119(12):1081-1087. doi: 10.11405/nisshoshi.119.1081.

Abstract

This is a case of a 61-year-old female who presented to our hospital with liver dysfunction without any symptoms. She was diagnosed with splenic arteriovenous fistula. About 8 months later, she visited the hospital again due to abdominal distention and diarrhea. Computerized tomography (CT) revealed splenic aneurysm, dilated splenic vein enhanced in the arterial phase, ascites, and intestinal edema. We considered that these findings were caused by portal hypertension due to splenic arteriovenous fistula. The splenic aneurysm was managed with coil embolization. Completion arteriography revealed the absence of flow into the splenic arteriovenous fistula. Surveillance CT scans at 2 months post-procedure confirmed complete occlusion of the aneurysm and arteriovenous fistula. There was no evidence of splenic infarction. The patient remained asymptomatic 1 year post-procedure. Asymptomatic splenic arteriovenous fistula is rare and needs immediate treatment due to the high probability of deterioration.

摘要

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