hunter's syndrome
Recently Published Documents


TOTAL DOCUMENTS

180
(FIVE YEARS 40)

H-INDEX

22
(FIVE YEARS 1)

Author(s):  
Yuya Kano ◽  
Chikako Sato ◽  
Yuto Uchida ◽  
Masahiro Muto ◽  
Keita Sakurai ◽  
...  

Stroke ◽  
2021 ◽  
Author(s):  
Robert W. Regenhardt ◽  
Mariel G. Kozberg ◽  
Adam A. Dmytriw ◽  
Justin E. Vranic ◽  
Christopher J. Stapleton ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Jasmine L. Taylor, MS ◽  
Ahmed Rashad, MD
Keyword(s):  

2021 ◽  
Vol 12 ◽  
Author(s):  
Noriya Enomoto ◽  
Kenji Yagi ◽  
Shunji Matsubara ◽  
Masaaki Uno

Bow hunter's syndrome (BHS) is most commonly caused by compression of the vertebral artery (VA). It has not been known to occur due to an extracranially originated posterior inferior cerebellar artery (PICA), the first case of which we present herein. A 71-year-old man presented with reproducible dizziness on leftward head rotation, indicative of BHS. On radiographic examination, the bilateral VAs merged into the basilar artery, and the left VA was predominant. The right PICA originated extracranially from the right VA at the atlas–axis level and ran vertically into the spinal canal. During the head rotation that induced dizziness, the right PICA was occluded, and a VA stenosis was revealed. Occlusion of the PICA was considered to be the primary cause of the dizziness. The patient underwent surgery to decompress the right PICA and VA via a posterior cervical approach. Following surgery, the patient's dizziness disappeared, and the stenotic change at the right VA and PICA improved. The PICA could be a causative artery for BHS when it originates extracranially at the atlas–axis level, and posterior decompression is an effective way to treat it.


2021 ◽  
Vol 429 ◽  
pp. 118285
Author(s):  
Ahamed Subir Humyun Kabir ◽  
Fazal Ghafoor ◽  
Krishnadas Nc ◽  
Mohammed Rafeeque

Author(s):  
João Tarrio ◽  
Catarina Mendes Pinto ◽  
Eduarda Maria Marinho Pinto ◽  
João Pedro Filipe ◽  
Cristina Ramos ◽  
...  

2021 ◽  
Vol 12 ◽  
pp. 451
Author(s):  
Seiji Shigekawa ◽  
Akihiro Inoue ◽  
Masahiko Tagawa ◽  
Daisuke Kohno ◽  
Takeharu Kunieda

Background: In spinal instrumentation surgery, safe and accurate placement of implants such as lateral mass screws and pedicle screws should be a top priority. In particular, C2 stabilization can be challenging due to the complex anatomy of the upper cervical spine. Here, we present a case of Bow Hunter’s syndrome (BHS) successfully treated by an O-arm-navigated atlantoaxial fusion. Case Description: A 53-year-old male presented with a 10-year history of repeated episodes of transient loss of consciousness following neck rotation to the right. Although the unenhanced magnetic resonance imaging showed no pathological findings, the MR angiogram with dynamic digital subtraction angiography revealed a dominant left vertebral artery (VA) and hypoplasia of the right VA. The latter study further demonstrated significant flow reduction in the left VA at the C1-C2 level when the head was rotated toward the right. With these findings of BHS, a C1-C2 decompression/posterior fusion using the Goel-Harms technique with O-arm navigation was performed. The postoperative cervical X-rays showed adequate decompression/fixation, and symptoms resolved without sequelae. Conclusion: C1-C2 posterior decompression/fusion effectively treats BHS, and is more safely/effectively performed utilizing O-arm navigation for C1-C2 screw placement.


2021 ◽  
Vol 43 (3) ◽  
pp. 349-353
Author(s):  
Yuta YOSHIMATSU ◽  
Satoru IDE ◽  
Shingo KAKEDA ◽  
Yu MURAKAMI ◽  
Satoshi FUKUMITSU ◽  
...  

2021 ◽  
Author(s):  
Nickalus R Khan ◽  
Turki Elarjani ◽  
Stephanie H Chen ◽  
Laszlo Miskolczi ◽  
Sheryl Strasser ◽  
...  

Abstract Rotational vertebral artery (VA) occlusion syndrome, also known as bow hunter's syndrome, is an uncommon variant of vertebrobasilar insufficiency typically occurring with head rotation.1-3 The most common presenting symptom is dizziness (76.8%), followed by visual abnormalities and syncope (50.4% and 40.4%, respectively).2 Osteophytic compression due to spinal spondylosis has been shown to be the most common etiology (46.2%), with other factors, such as a fibrous band, muscular compression, or spinal instability, being documented.1,2 Treatment is dependent on the level and site of VA compression with anterior, anterolateral, or posterior approaches being described.1,4 We present the case of a 72-yr-old male with osteophytic compression of the V3 segment of the vertebral artery at the occipital-cervical junction. The patient underwent a C1 hemilaminectomy and removal of osteophytic compression from the occipital-cervical joint. The patient had complete resolution of compression of his vertebral artery on postoperative imaging and remained neurologically intact following the procedure. We review the literature on this topic, the technical nuances of the procedure performed, and review the different treatment modalities available for this rare condition.1-11  The patient consented to the procedure and to publication of their image.


2021 ◽  
pp. jnnp-2021-326462
Author(s):  
Tahereh Toluian ◽  
Daniel Volterra ◽  
Andrea Gioppo ◽  
Paolo Rigamonti

Sign in / Sign up

Export Citation Format

Share Document