Spontaneous Thrombosis of a Middle Meningeal Arteriovenous Fistula With Subsequent Pseudoaneurysm Formation: Case Report and Review of Literature

P. Nazari, P. Golnari, M. Sukumaran, A. Shaibani, M. Hurley, S. Ansari, M. Potts, B. Jahromi
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引用次数: 3

Abstract

Middle meningeal artery (MMA) pseudoaneurysms and middle meningeal arteriovenous fistulas (MMAVFs) are rarely reported after head injury. We report an unusual case of delayed MMA pseudoaneurysm formation after spontaneous thrombosis of an MMAVF, and review existing literature on MMAVF treatment and results. A 59-yr-old male presented with a 5-d history of worsening left-sided headaches, followed by nausea, lethargy, and difficulty with speech. Non-contrast computed tomography demonstrated a left temporal intraparenchymal hemorrhage (IPH) and an acute left-sided subdural hematoma (SDH). Cerebral angiography found abnormal shunting between the right MMA and the right sphenoparietal sinus, consistent with an MMAVF. During the course of admission, the patient's neurological condition deteriorated requiring craniotomy for evacuation of SDH and IPH. Given the presumed incidental nature of the contralateral MMAVF, conservative management was recommended. Follow-up imaging 2 mo after surgery revealed spontaneous thrombosis of the right MMAV. Repeat imaging 5 mo later revealed an MMA pseudoaneurysm at the prior fistulous site, which was subsequently embolized with Onyx, occluding the pseudoaneurysm and the MMA both proximal and distal to the pseudoaneurysm. Spontaneous thrombosis of an MMAVF is rare and only seen in 13.1% of cases. However, subsequent delayed formation of an MMA pseudoaneurysm has not been described. Our case therefore demonstrates that MMAVF thrombosis may not indicate complete healing of the underlying injury to the MMA, and suggests the need for continued follow-up of such lesions despite initial apparent resolution.
自发性脑膜中动静脉瘘血栓形成并发假性动脉瘤:1例报告及文献回顾
脑膜中动脉假性动脉瘤和脑膜中动静脉瘘在颅脑损伤后发生的报道很少。我们报告一例不寻常的mavf自发性血栓形成后延迟MMA假性动脉瘤形成的病例,并回顾现有的关于MMAVF治疗和结果的文献。一名59岁男性,出现左侧头痛加重5天病史,随后出现恶心、嗜睡和言语困难。非对比ct显示左侧颞实质内出血(IPH)和急性左侧硬膜下血肿(SDH)。脑血管造影发现右侧中动脉和右侧蝶顶窦之间有异常分流,符合MMAVF。在入院过程中,患者神经系统状况恶化,需要开颅以排出SDH和IPH。考虑到对侧MMAVF的偶发性,建议采用保守治疗。术后2个月随访影像显示右侧MMAV自发性血栓形成。5个月后重复成像显示先前的瘘处有MMA假性动脉瘤,随后用Onyx栓塞,阻塞假性动脉瘤和假性动脉瘤的近端和远端MMA。自发性血栓形成的MMAVF是罕见的,只有13.1%的病例。然而,随后延迟形成的MMA假性动脉瘤尚未被描述。因此,我们的病例表明,MMAVF血栓形成可能并不表明MMA的潜在损伤完全愈合,并提示尽管最初明显消退,但仍需要继续随访此类病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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