Spontaneous Thrombosis of a Middle Meningeal Arteriovenous Fistula With Subsequent Pseudoaneurysm Formation: Case Report and Review of Literature. Issue 3 (2nd July 2020)

• Record Type: Journal Article
• Authors: Nazari, Pouya; Golnari, Pedram; Sukumaran, Madhav; Shaibani, Ali; Hurley, Michael C; Ansari, Sameer A; Potts, Matthew B; Jahromi, Babak S
• Is Part Of: Neurosurgery open. Volume 1:Issue 3(2020)
• Publication Date: 2020-07-02
• Subjects: Middle meningeal artery -- Arteriovenous fistula -- Pseudoaneurysm -- Spontaneous thrombosis -- Case report; Nervous system -- Surgery -- Periodicals; 617.48
• DOI: 10.1093/neuopn/okaa006
• Languages: English
• ISSNs: 2633-0873

Abstract

ABSTRACT: BACKGROUND AND IMPORTANCE: 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. CLINICAL PRESENTATION: 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. CONCLUSION: 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.