Open Access
CC-BY-NC-ND 4.0 · J Neurol Surg Rep 2017; 78(01): e37-e39
DOI: 10.1055/s-0037-1600136
Case Report
Georg Thieme Verlag KG Stuttgart · New York

A Previously Unreported Arterial Variant of the Suboccipital Region Based on Cadaveric Dissection

Christian Fisahn
1   Swedish Medical Center, Swedish Neuroscience Institute, Seattle, Washington, United States
2   Seattle Science Foundation, Seattle, Washington, United States
,
Brittni Burgess
2   Seattle Science Foundation, Seattle, Washington, United States
,
Joe Iwanaga
2   Seattle Science Foundation, Seattle, Washington, United States
,
Fernando Alonso
1   Swedish Medical Center, Swedish Neuroscience Institute, Seattle, Washington, United States
,
Jens R. Chapman
1   Swedish Medical Center, Swedish Neuroscience Institute, Seattle, Washington, United States
,
Rod J. Oskouian
1   Swedish Medical Center, Swedish Neuroscience Institute, Seattle, Washington, United States
,
R. Shane Tubbs
2   Seattle Science Foundation, Seattle, Washington, United States
› Institutsangaben
Weitere Informationen

Publikationsverlauf

27. Oktober 2016

10. Februar 2017

Publikationsdatum:
14. März 2017 (online)

Preview

Abstract

Introduction Several arterial variants have been reported to occur around the posterior arch of the atlas. Understanding the various anomalies and diagnosing them preoperatively can dramatically reduce the risk of surgical insult during neurosurgical procedures. Herein we report a case of an arterial variant found just below the posterior arch of C1.

Case Report During the routine dissection of the suboccipital region via a posterior approach, an unusual bulge was identified just inferior to the inferior capitis oblique muscle. With further dissection, the structure was identified as a tortuous internal carotid artery.

Conclusion Arterial variants around the posterior arch of C1 are surgically significant and can result in catastrophic injuries if unappreciated. Most of these variants will be related to the vertebral artery. To our knowledge, an arterial variant of the internal carotid artery in this location, as reported herein, has not been previously reported.

Informed Consent

Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent form is available for review by the Editor-in-Chief of this journal on request.