Siablis Dimitrios, Papathanassiou Zafiria-G, Karnabatidis Dimitrios, Christeas Nikolaos, Katsanos Konstantinos, Vagianos Constantine
Department of Radiology, Medical School, University of Patras, Rio 26504 Patras, Greece.
World J Gastroenterol. 2006 Jul 14;12(26):4264-6. doi: 10.3748/wjg.v12.i26.4264.
Splenic arteriovenous fistula (SAVF) accounts for an unusual but well-documented treatable cause of portal hypertension([1-4]). A case of a 50-year-old multiparous female who developed suddenly portal hypertension due to SAVF formation is presented. The patient suffered from repeated episodes of haematemesis and melaena during the past twelve days and thus was emergently admitted to hospital for management. Clinical and laboratory investigations established the diagnosis of portal hypertension in the absence of liver parenchymal disease. Endoscopy revealed multiple esophageal bleeding varices. Abdominal computed tomography (CT) and transfemoral celiac arteriography documented the presence of a tortuous and aneurysmatic splenic artery and premature filling of an enlarged splenic vein, findings highly suggestive of an SAVF. The aforementioned vascular abnormality was successfully treated with percutaneous transcatheter embolization. Neither recurrence nor other complications were observed.
脾动静脉瘘(SAVF)是门静脉高压症一种罕见但有充分文献记载的可治疗病因([1-4])。本文报告一例50岁经产妇,因形成脾动静脉瘘而突然发生门静脉高压症。患者在过去12天内反复出现呕血和黑便,因此紧急入院治疗。临床和实验室检查在无肝实质疾病的情况下确诊为门静脉高压症。内镜检查发现多处食管静脉曲张出血。腹部计算机断层扫描(CT)和经股动脉腹腔动脉造影显示存在迂曲且呈动脉瘤样的脾动脉以及脾静脉提前显影,这些表现高度提示脾动静脉瘘。上述血管异常通过经皮经导管栓塞术成功治疗。未观察到复发及其他并发症。