Ono Shigeshi, Obara Hideaki, Shimoda Masayuki, Kitagawa Yuko
Department of Surgery, Keio University School of Medicine, Tokyo, Japan.
Department of Pathology, Keio University School of Medicine, Tokyo, Japan.
BMJ Case Rep. 2015 Apr 22;2015:bcr2015209688. doi: 10.1136/bcr-2015-209688.
Splenic arteriovenous fistula (SAVF) without a splenic arterial aneurysm is a rare entity and may either be congenital or acquired. Acquired SAVFs are commonly due to adjacent splenic arterial aneurysm rupture, trauma or infection. We report a large idiopathic SAVF in a 50-year-old woman who had no symptoms. CT showed that the fistula was around the splenic hilum and no other specific findings. SAVF has a risk of sudden onset of portal hypertension and it should be treated as soon as diagnosed. Endovascular treatment for SAVF is now being performed successfully with increasing frequency, however, there is still no definitive evidence of treatment for SAVF. Treatment options should be determined appropriately depending on individual case characteristics and vascular anatomical variations. Our case was treated successfully with splenectomy, and long-term results are good without need of reintervention.
无脾动脉瘤的脾动静脉瘘(SAVF)是一种罕见的病症,可能是先天性的,也可能是后天获得性的。后天性SAVF通常是由于相邻的脾动脉瘤破裂、外伤或感染所致。我们报告一例50岁无症状女性的巨大特发性SAVF。CT显示瘘管位于脾门周围,无其他特异性表现。SAVF有门静脉高压突然发作的风险,一经诊断应立即治疗。目前,SAVF的血管内治疗成功率越来越高,但对于SAVF的治疗仍没有确凿的证据。应根据个体病例特征和血管解剖变异适当确定治疗方案。我们的病例通过脾切除术成功治愈,长期效果良好,无需再次干预。