Lanzino G, Jensen M E, Kongable G L, Kassell N F
Department of Neurological Surgery, University of Virginia Health Sciences Center, Charlottesville.
Acta Neurochir (Wien). 1994;129(3-4):140-5. doi: 10.1007/BF01406493.
Dural arteriovenous malformations (dAVMs) are uncommon lesions that constitute about 12% of all the arteriovenous malformations. Depending on the location and the hemodynamics of the lesion, bruit, focal neurological deficit, and visual symptoms represent the more common presentation modalities. Although uncommon, intracranial hemorrhage can occur. In the present study, we report six patients with dural arteriovenous malformation that presented with intracranial hemorrhage. In five cases the hemorrhage was intraparenchymal (localized to the parietooccipital area in three), while it was confined to the subarachnoid space in the remaining one. The dAVM involved the transverse sinus in three cases, was based along the tentorial incisura in two, and was at the level of the torcular Herophili in one. Leptomeningeal drainage was present in all the cases. Aneurysmal dilatation of the draining vein(s) was identified in three. Sinus stenosis/occlusion was identified in two of the four patients with a dAVM draining into a major dural sinus. Four patients underwent pre-operative embolization, and all patients had surgical resection of their lesions. Anatomical cure, as defined by absence of any residual dAVM on postoperative angiogram, was achieved in all six patients. We conclude that several findings such as leptomeningeal drainage, location outside a major venous sinus, variceal dilatation, sinus stenosis/occlusion increase the risk of bleeding and are frequently observed in those dAVMs that present with intracranial hemorrhage. Recognition of these angiographic features is critical in planning a therapeutic approach tailored to the characteristics of the individual case. When these angiographic findings are present, prompt and definitive treatment is mandatory.(ABSTRACT TRUNCATED AT 250 WORDS)
硬脑膜动静脉畸形(dAVM)是一种罕见的病变,约占所有动静脉畸形的12%。根据病变的位置和血流动力学,血管杂音、局灶性神经功能缺损和视觉症状是较常见的表现形式。虽然不常见,但颅内出血仍可能发生。在本研究中,我们报告了6例以颅内出血为表现的硬脑膜动静脉畸形患者。5例出血为脑实质内出血(3例局限于顶枕区),其余1例局限于蛛网膜下腔。3例dAVM累及横窦,2例位于小脑幕切迹缘,1例位于窦汇水平。所有病例均存在软脑膜引流。3例发现引流静脉瘤样扩张。在4例dAVM引流至主要硬脑膜窦的患者中,2例发现窦狭窄/闭塞。4例患者术前行栓塞治疗,所有患者均接受了病变切除术。所有6例患者术后血管造影均未发现残留dAVM,达到了解剖学治愈。我们得出结论,软脑膜引流、主要静脉窦外的位置、静脉曲张样扩张、窦狭窄/闭塞等多种表现增加了出血风险,且在以颅内出血为表现的dAVM中经常观察到。认识这些血管造影特征对于制定针对个体病例特点的治疗方案至关重要。当出现这些血管造影表现时,必须及时进行明确的治疗。(摘要截断于250字)