Dural arteriovenous fistulas of the hypoglossal canal: systematic review on imaging anatomy, clinical findings, and endovascular management

Author:

Spittau Björn1,Millán Diego San2,El-Sherifi Saad3,Hader Claudia34,Singh Tejinder Pal5,Motschall Edith6,Vach Werner6,Urbach Horst3,Meckel Stephan3

Affiliation:

1. Institute for Anatomy and Cell Biology, Department of Molecular Embryology, Albert-Ludwigs-University Freiburg;

2. Neuroradiology Unit, Department of Diagnostic and Interventional Radiology, Centre Hospitalier du Centre du Valais, Hôpital de Sion;

3. Department of Neuroradiology, University Hospital Freiburg;

4. Neuroradiology Unit, Institute of Radiology, Kantonsspital St. Gallen, Switzerland; and

5. Neurological Intervention and Imaging Service of Western Australia, Sir Charles Gairdner & Royal Perth Hospitals, Nedlands, Western Australia, Australia

6. Center for Medical Biometry and Medical Informatics, Medical Center–University of Freiburg, Germany;

Abstract

Dural arteriovenous fistulas (DAVFs) of the hypoglossal canal (HCDAVFs) are rare and display a complex angiographic anatomy. Hitherto, they have been referred to as various entities (for example, “marginal sinus DAVFs”) solely described in case reports or small series. In this in-depth review of HCDAVF, the authors describe clinical and imaging findings, as well as treatment strategies and subsequent outcomes, based on a systematic literature review supplemented by their own cases (120 cases total). Further, the involved craniocervical venous anatomy with variable venous anastomoses is summarized. Hypoglossal canal DAVFs consist of a fistulous pouch involving the anterior condylar confluence and/or anterior condylar vein with a variable intraosseous component. Three major types of venous drainage are associated with distinct clinical patterns: Type 1, with anterograde drainage (62.5%), mostly presents with pulsatile tinnitus; Type 2, with retrograde drainage to the cavernous sinus and/or orbital veins (23.3%), is associated with ocular symptoms and may mimic cavernous sinus DAVF; and Type 3, with cortical and/or perimedullary drainage (14.2%), presents with either hemorrhage or cervical myelopathy. For Types 1 and 2 HCDAVF, transvenous embolization demonstrates high safety and efficacy (2.9% morbidity, 92.7% total occlusion). Understanding the complex venous anatomy is crucial for planning alternative approaches if standard transjugular access is impossible. Transarterial embolization or surgical disconnection (morbidity 13.3%–16.7%) should be reserved for Type 3 HCDAVFs or lesions with poor venous access. A conservative strategy could be appropriate in Type 1 HCDAVF for which spontaneous regression (5.8%) may be observed.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Genetics,Animal Science and Zoology

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