Dural and cavernous arteriovenous fistulas

2010 ◽  
pp. 608-614
Author(s):  
George Samandouras

Chapter 9.14 covers dural and cavernous arteriovenous fistulas, including duralarteriovenous fistula (DAVF), carotid cavernous fistula (CCF), and vein of Galen malformation (VOGAM).

2019 ◽  
Vol 127 ◽  
pp. 216-219 ◽  
Author(s):  
Mohammad Ghorbani ◽  
Sina Asaadi ◽  
Christoph Wipplinger ◽  
Christoph J. Griessenauer ◽  
Fatemeh Zangi-Abadi ◽  
...  

2017 ◽  
Vol 24 (1) ◽  
pp. 82-87 ◽  
Author(s):  
Dan Meila ◽  
Cynthia Schmidt ◽  
Katharina Melber ◽  
Dominik Grieb ◽  
Cornelius Jacobs ◽  
...  

The association of dural arteriovenous fistulas (DAVF) in children with Vein of Galen malformation (VGM) has recently been reported for the first time. In a larger series of cases treated with transarterial NBCA embolization, 30% had DAVF. We wanted to analyze the development of DAVF in our cohort of children with VGM and to evaluate whether their occurrence depends on different treatment timing and embolic materials. We analyzed 43 VGM cases treated with a combined transarterial and transvenous approach between 2003 and 2016. In our early series until 2011, we used coils solely in 21 children. Since 2012, 22 children were treated with the combination of coils and Onyx. In the early series treated with coils solely, no case presented initially with or developed DAVF over time on follow-up angiograms. In our recent series we found four cases (9%) with DAVF. In two patients (5%), DAVF were found on the initial angiogram. Both patients presented at our department at age >2 years and were not treated elsewhere before. One patient (2%) presented at our department with too proximal occlusion of arterial feeders performed at another institution before. Only one patient (2%) developed DAVF in our department after the transarterial use of Onyx. Interestingly, this child did not develop DAVF as long as we used coils solely and his DAVF was localized exactly where an Onyx cast was identified. In conclusion, delayed and incomplete treatment may have a considerable impact on the occurrence of DAVF in VGM.


1981 ◽  
Vol 54 (2) ◽  
pp. 252-256 ◽  
Author(s):  
Shigeo Toya ◽  
Ryuzoh Shiobara ◽  
Jiroh Izumi ◽  
Youichi Shinomiya ◽  
Hayao Shiga ◽  
...  

✓ The authors report two cases of spontaneous carotid-cavernous fistula that occurred during pregnancy. One patient was a 21-year-old woman whose symptoms improved and in whom disappearance of the carotid-cavernous fistula was confirmed by cerebral angiography after she aborted in the 12th week of pregnancy. The other patient was a 25-year-old woman in whom a carotid-cavernous fistula occurred at about the 28th week of pregnancy. The symptoms became aggravated 3 weeks after a normal delivery. Carotid-cavernous fistula was confirmed by cerebral angiography, and the clinical symptoms then improved. On the basis of cerebral angiographic findings, both patients were considered to have dural arteriovenous fistulas in the region of the cavernous sinus and both demonstrated spontaneous improvement.


2003 ◽  
Vol 9 (1) ◽  
pp. 57-63 ◽  
Author(s):  
Y.-C. Weon ◽  
D. Ducreux ◽  
H. Alvarez ◽  
P. Lasjaunias

Vein of Galen Aneurysmal Malformations (VAGMs) are uncommon vascular malformations associated with dilatation of the vein of Galen embryonic forerunner with single or multiple direct arteriovenous fistulas within its wall without direct reflux into normal cerebral veins. We describe a patient with a late neurological onset presenting a classic VGAM complicated by secondary thalamic capillary angioectasia imaged with MR perfusion. In our patient, abnormal MR perfusion parameters were not seen on conventional MRI; they probably reflect underlying venous hypertension. They were located in areas involved in motor neurological deficit.


2015 ◽  
Vol 8 (9) ◽  
pp. e35-e35 ◽  
Author(s):  
Daniel Felbaum ◽  
Swathi Chidambaram ◽  
Robert Bryan Mason ◽  
Rocco A Armonda ◽  
Ai Hsi Liu

Vertebral–venous fistulas (VVF), or vertebral–vertebral arteriovenous fistulas, are an uncommon clinical entity. Typically, they present as a result of a direct vascular connection between an extracranial branch of the vertebral artery or its radicular components and the epidural venous plexus. These may manifest with signs and symptoms referable to cervical myelopathy secondary to compression or steal phenomenon. To our knowledge, this is the first case to identify a patient who presented with classic ocular symptoms attributable to a carotid cavernous fistula but secondary to a VVF. We present its treatment and clinical outcome. In addition, we present a brief literature review surrounding this uncommon disease.


2006 ◽  
Vol 58 (suppl_1) ◽  
pp. ONS-E170-ONS-E170 ◽  
Author(s):  
Louis P. Caragine ◽  
Van V. Halbach ◽  
Chris F. Dowd ◽  
Randall T. Higashida

Abstract OBJECTIVE AND IMPORTANCE Intraorbital arteriovenous fistulas (AVF) of the ophthalmic veins are an extremely rare phenomenon. This article describes two such cases treated solely by transvenous occlusion and not hitherto described in the literature. METHODS AND RESULTS: Two women, aged 51 and 63 years old, presented with proptosis and chemosis mimicking a carotid-cavernous fistula. In both cases, cerebral angiography revealed an intraorbital dural AVF of the superior and inferior ophthalmic vein, respectively. Both patients underwent transvenous ablation of the dural AVF retrograde via the facial vein and subsequently had complete resolution of the presenting symptoms. METHODS: Ophthalmic vein fistulas are a rare form of AVF with presenting symptoms mimicking those of carotid cavernous fistulae. This report describes two cases of ophthalmic vein fistulas successfully treated and angiographically obliterated via transvenous embolization with resolution of the patient's presenting symptoms.


2009 ◽  
Vol 19 (5) ◽  
pp. 894-896
Author(s):  
Sarah Zafar ◽  
Saemah N. Zafar ◽  
Ayesha Khan ◽  
Saerah Iffat Zafar

2019 ◽  
pp. 116-118
Author(s):  
I.N. Pakhirko ◽  
◽  
M.N. Ponomareva ◽  
E.Y. Ponomareva ◽  
I.A. Aymurzina ◽  
...  

Perfusion ◽  
2021 ◽  
pp. 026765912110015
Author(s):  
Alex Robertson ◽  
Nagarajan Muthialu ◽  
Mike Broadhead

We present a dissection of the patent ductus arteriosus and pulmonary artery for surgical repair utilising cardiopulmonary bypass in the setting of vein of Galen malformation. Several strategies were employed to attenuate the cerebral shunt including pH-stat, high cardiac index, restrictive venous drainage, continuous ventilation and deep hypothermic circulatory arrest. The patient recovered from surgery with no apparent neurological sequelae.


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