scholarly journals A case of dural arteriovenous fistula at the craniocervical junction with intramedullary hemorrhage in the medulla oblongata caused by venous congestion

Nosotchu ◽  
2021 ◽  
Author(s):  
Kazuki Sogawa ◽  
Koichi Satoh ◽  
Masaaki Korai ◽  
Mami Hanaoka ◽  
Tadashi Yamaguchi ◽  
...  
2015 ◽  
Vol 21 (6) ◽  
pp. 724-727 ◽  
Author(s):  
Raoul Pop ◽  
Monica Manisor ◽  
Ziad Aloraini ◽  
Salvatore Chibarro ◽  
Francois Proust ◽  
...  

Intracranial dural arteriovenous fistulas (dAVFs) with perimedullary drainage represent a rare subtype of intracranial dAVF. Patients usually experience slowly progressive ascending myelopathy and/or lower brainstem signs. We present a case of foramen magnum dural arteriovenous fistula with an atypical clinical presentation. The patient initially presented with a generalised tonic-clonic seizure and no signs of myelopathy, followed one month later by rapidly progressive tetraplegia and respiratory insufficiency. The venous drainage of the fistula was directed both to the left temporal lobe and to the perimedullary veins (type III + V), causing venous congestion and oedema in these areas and explaining this unusual combination of symptoms. Rotational angiography and overlays with magnetic resonance imaging volumes were helpful in delineating the complex anatomy of the fistula. After endovascular embolisation, there was complete remission of venous congestion on imaging and significant clinical improvement. To our knowledge, this is the first report of a craniocervical junction fistula presenting with epilepsy.


2012 ◽  
Vol 3 (1) ◽  
pp. 53 ◽  
Author(s):  
Takaaki Miyagishima ◽  
Masato Inoue ◽  
Hiroyasu Ohno ◽  
Kanehiro Hasuo ◽  
Tetsuo Hara ◽  
...  

Stroke ◽  
2021 ◽  
Author(s):  
Ryan M. Naylor ◽  
Britney Topinka ◽  
Lorenzo Rinaldo ◽  
Jaclyn Jacobi ◽  
Bryan Neth ◽  
...  

2013 ◽  
Vol 10 (1) ◽  
pp. E178-E182 ◽  
Author(s):  
John D. Nerva ◽  
Danial K. Hallam ◽  
Basavaraj V. Ghodke

Abstract BACKGROUND AND IMPORTANCE: An intraosseous dural arteriovenous fistula (DAVF) is a rare cerebrovascular disease. The fistulous connection occurs within intraosseous diploic or transosseous emissary veins causing dilated intraosseous vascular pouches. To the authors' knowledge, this report describes the first percutaneous transfacial direct embolization of an intraosseous DAVF. CLINICAL PRESENTATION: A man in his 50s with blue rubber bleb nevus syndrome presented with headaches, imbalance, decreased visual acuity bilaterally, and left eye proptosis and chemosis. Imaging demonstrated an extensive intraosseous DAVF with dilated intraosseous vascular pouches throughout his cranial base and intraorbital venous congestion. He underwent staged endovascular treatment with the goal to improve his ocular symptoms. Transarterial and transvenous approaches failed to provide adequate access to the intraosseous vascular pouches. A direct, percutaneous transfacial approach was used to access the pouches for embolization with coils and liquid embolic material. Postoperative angiography demonstrated successful embolization of the pouch within the left pterygoid wing, reduced opacification of the intraosseous fistula, and elimination of intraorbital venous congestion. At 9-month follow-up, the patient's headaches had resolved, and his ocular symptomatology had improved. CONCLUSION: Endovascular access to an intraosseous DAVF is limited by the size and location of the intraosseous vascular pouches. In this case, a direct transfacial approach under image guidance facilitated access and embolization, which led to an improvement in the patient's symptoms. This technique is a novel approach for DAVF management.


2007 ◽  
Vol 1 (1) ◽  
pp. 26-30 ◽  
Author(s):  
Tomoki OHSHIMA ◽  
Shigeru MIYACHI ◽  
Takashi IZUMI ◽  
Arihito TSURUMI ◽  
Takeshi KINKORI ◽  
...  

Author(s):  
Siu Kei Samuel Lam ◽  
Sai Lok Chu ◽  
Shing Chau Yuen ◽  
Kwong Yui Yam

AbstractWe report a case of craniocervical junction dural arteriovenous fistula (dAVF) presented with myelopathy and normal pressure hydrocephalus, and was treated with hybrid approach of embolization and surgical disconnection. A 68-year-old gentleman presented with 1 year history of unsteady gait and sphincter disturbance. Magnetic resonance imaging (MRI) showed abnormally enlarged and tortuous vessels over right cerebellomedullary cistern. Digital subtraction angiogram (DSA) showed Cognard's type-V dAVF at craniocervical junction. Catheter embolization was performed via external carotid artery and finally surgical disconnection was done with far lateral approach (Fig. 1). Postoperative DSA showed no more arteriovenous shunting (Fig. 2). Clinically the patient improved after a course of rehabilitation. Dural AVF at craniocervical junction is rare and its clinical presentation can be highly variable from subarachnoid hemorrhage to brainstem dysfunction. Identification of the exact fistula site is essential in surgical planning. Surgery is effective and safe to achieve complete obliteration and good clinical outcome.1 2 3 4 5 6 The link to the video can be found at: https://youtu.be/xI48stSlWpY.


Nosotchu ◽  
2015 ◽  
Vol 37 (2) ◽  
pp. 107-110
Author(s):  
Takeo Baba ◽  
Akinori Yamamura ◽  
Riichiro Kishimoto ◽  
Kentaro Toyama ◽  
Katsuyuki Nunomura ◽  
...  

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