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前颅窝硬脑膜动静脉畸形

Dural arteriovenous malformations in the anterior cranial fossa.

作者信息

Başkaya M K, Suzuki Y, Seki Y, Negoro M, Ahmed M, Sugita K

机构信息

Department of Neurosurgery, Nagoya University School of Medicine, Japan.

出版信息

Acta Neurochir (Wien). 1994;129(3-4):146-51. doi: 10.1007/BF01406494.

Abstract

Two cases of dural arteriovenous malformation (DAVM) fed by the anterior ethmoidal artery in the anterior cranial fossa are reported, one of them examined by magnet resonance imaging (MRI). Only one other case with MRI findings so far has been published. Fourty-eight previously reported cases are reviewed. One of our patients presented with subdural haematoma (SDH) without subarachnoid or intracerebral haemorrhage. The other patient had a nasal bleed without any neurological manifestations. In comparison with previously reported cases, the clinical manifestation of our cases is infrequent (1 patient with nasal bleed, and 2 patients with pure SDH that is 2 and 4%, respectively, in the literature). Feeder was the anterior ethmoidal artery either unilateral or bilateral. Drainage of DAVMs was through a markedly dilated vascular sac into the superior sagittal sinus (SSS). The high incidence of haemorrhage from DAVM in the anterior fossa is related to this vascular sac. Magnetic resonance imaging (MRI) showed a flow void area in the left frontal region on T 1-weighted images in one case. These cases were treated by surgical excision of the malformation with good results. Aetiology, clinical presentation, and treatment of these rare DAVMs in the anterior cranial fossa is discussed.

摘要

报告了两例由前颅窝筛前动脉供血的硬脑膜动静脉畸形(DAVM),其中一例接受了磁共振成像(MRI)检查。迄今为止,仅有另一例有MRI检查结果的病例被发表。对先前报道的48例病例进行了回顾。我们的一名患者表现为硬膜下血肿(SDH),无蛛网膜下腔或脑内出血。另一名患者有鼻出血,无任何神经学表现。与先前报道的病例相比,我们病例的临床表现并不常见(1例鼻出血,2例单纯硬膜下血肿,在文献中分别占2%和4%)。供血动脉为单侧或双侧筛前动脉。DAVM通过一个明显扩张的血管囊引流至上矢状窦(SSS)。前颅窝DAVM出血的高发生率与这个血管囊有关。磁共振成像(MRI)在一例T1加权图像上显示左额叶区域有血流空洞区。这些病例通过手术切除畸形取得了良好效果。讨论了这些前颅窝罕见DAVM的病因、临床表现及治疗。

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