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前颅窝未破裂硬脑膜动静脉瘘的手术治疗:7年自然病史

Surgical management of an unruptured dural arteriovenous fistula of the anterior cranial fossa: natural history for 7 years.

作者信息

Im So-Hyang, Oh Chang Wan, Han Dae Hee

机构信息

Department of Neurosurgery, Seoul National University College of Medicine, Clinical Research Institute, Seoul National University Hospital, Seoul, South Korea.

出版信息

Surg Neurol. 2004 Jul;62(1):72-5; discussion 75. doi: 10.1016/j.surneu.2003.07.018.

Abstract

BACKGROUND

Anterior cranial fossa dural arteriovenous fistulas (DAVFs), unlike those in other locations, form a distinct subgroup because of a high incidence of intracerebral hemorrhage and their unique anatomy. We surgically obliterated an unruptured anterior cranial fossa DAVF because the venous aneurysm in the DAVF increased in size during the follow-up period and we present the clinical symptoms, the natural history for a 7-year period before operation, the radiologic findings, and surgical management. This is the first case report in which the growth of a preexisting venous aneurysm in an anterior fossa DAVF was identified. The possible pathogeneses of the rupture of anterior cranial DAVFs are discussed.

CASE DESCRIPTION

A 68-year-old man presented with diplopia, retro-orbital headache, and loss of consciousness. Cerebral angiography revealed an anterior cranial fossa DAVF. The primary source of arterial supply was from the ipsilateral anterior ethmoidal artery in combination with the contralateral anterior ethmoidal artery and other less prominent feeding vessels from the external carotid artery (ECA). Venous drainage was through the superior sagittal sinus via dilated pial veins. In addition, a subfrontal pial vein drained toward the region of the sphenoparietal and cavernous sinuses. The detection of the growth of a venous aneurysm 7 years after the initial evaluation prompted an aggressive therapeutic decision on considering a future catastrophic rupture risk. The vascular malformation was approached via a low-frontal craniotomy. A venous aneurysm with a dural feeder was encountered near the site of the anastomosis. The vascular connection between the dura of the cribriform plate and the pial vessels was completely occluded. Postoperative angiography confirmed the complete obliteration of the DAVF.

CONCLUSION

In this case, we confirmed an increase in the size of a venous aneurysm of an anterior cranial fossa DAVF. Our findings support the belief that the catastrophic intracranial hemorrhage in an anterior cranial fossa DVAF may occur in the setting of increased hemodynamic pressure of its draining venous channel.

摘要

背景

前颅窝硬脑膜动静脉瘘(DAVF)与其他部位的DAVF不同,因其脑出血发生率高及独特的解剖结构而形成一个独特的亚组。我们对一例未破裂的前颅窝DAVF进行了手术闭塞,原因是该DAVF中的静脉瘤在随访期间增大,我们在此介绍其临床症状、术前7年的自然病史、影像学表现及手术治疗情况。这是首例报告前颅窝DAVF中原有静脉瘤生长的病例。文中还讨论了前颅窝DAVF破裂的可能发病机制。

病例描述

一名68岁男性出现复视、眶后头痛和意识丧失。脑血管造影显示为前颅窝DAVF。动脉供血的主要来源是同侧筛前动脉,联合对侧筛前动脉以及来自颈外动脉(ECA)的其他不太明显的供血血管。静脉引流通过扩张的软脑膜静脉经上矢状窦进行。此外,一条额叶下软脑膜静脉引流至蝶顶窦和海绵窦区域。初次评估7年后检测到静脉瘤生长,鉴于未来有灾难性破裂风险,促使我们做出积极的治疗决策。通过低位额部开颅手术处理该血管畸形。在吻合部位附近发现一个带有硬脑膜供血支的静脉瘤。筛板硬脑膜与软脑膜血管之间的血管连接被完全闭塞。术后血管造影证实DAVF已完全闭塞。

结论

在本病例中,我们证实了前颅窝DAVF的静脉瘤大小增加。我们的发现支持这样一种观点,即前颅窝DVAF发生灾难性颅内出血可能是在其引流静脉通道血流动力学压力增加的情况下。

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