Share:
Share this content in WeChat
X
Case Report
Craniocervical junction malformation combined with classic Dejerine syndrome: One case report
WANG Haoyue  GE Zhaoming 

Cite this article as: Wang HY, GE ZM. Craniocervical junction malformation combined with classic Dejerine syndrome: One case report[J]. Chin J Magn Reson Imaging, 2022, 13(8): 94-95, 100. DOI:10.12015/issn.1674-8034.2022.08.019.


[Keywords] magnetic resonance imaging;acute ischemic stroke;Dejerine syndrome;atlantoaxial dislocation;craniovertebral junction malformation

WANG Haoyue   GE Zhaoming*  

Department of Neurology, Lanzhou University Second Hospital, Lanzhou 730030, China

Ge ZM, E-mail: 13893285120@163.com

Conflicts of interest   None.

ACKNOWLEDGMENTS Lanzhou Talent Innovation and Technology Start-up Programme (No. 2020-RC-93); "Cuiying Scientific and Technological Innovation Plan" of the Second Hospital of Lanzhou University (No. CJ209-BJ01).
Received  2022-03-26
Accepted  2022-05-23
DOI: 10.12015/issn.1674-8034.2022.08.019
Cite this article as: Wang HY, GE ZM. Craniocervical junction malformation combined with classic Dejerine syndrome: One case report[J]. Chin J Magn Reson Imaging, 2022, 13(8): 94-95, 100. DOI:10.12015/issn.1674-8034.2022.08.019.

[1]
Saccheri P, Travan L. The craniovertebral junction, between osseous variants and abnormalities: insight from a paleo-osteological study[J]. Anat Sci Int, 2022, 97(2): 197-212. DOI: 10.1007/s12565-021-00642-7.
[2]
Fukuoka T, Takeda H, Dembo T, et al. Clinical review of 37 patients with medullary infarction[J]. J Stroke Cerebrovasc Dis, 2012, 21(7): 594-599. DOI: 10.1016/j.jstrokecerebrovasdis.2011.01.008.
[3]
Salunke P, Karthigeyan M, Ahuja CK, et al. An Unusual Cause of Vertebrobasilar Insufficiency in a Case of Atlantoaxial Dislocation with Anomalous Vertebral Artery[J]. World Neurosurg, 2020, 138(6): 193-196. DOI: 10.1016/j.wneu.2020.02.144.
[4]
Kulkarni GB, Mustare V, Pruthi N, et al. Profile of patients with craniovertebral junction anomalies with posterior circulation strokes[J]. J Stroke Cerebrovasc Dis, 2014, 23(10): 2819-2826. DOI: 10.1016/j.jstrokecerebrovasdis.2014.07.003.
[5]
Singer WD, Haller JS, Wolpert SM. Occlusive vertebrobasilar artery disease associated with cervical spine anomaly[J]. Am J Dis Child, 1975, 129(4): 492-495. DOI: 10.1001/archpedi.1975.02120410066018.
[6]
Verma R, Sahu R, Ojha BK, et al. Thalamic syndrome as the heralding manifestation of atlantoaxial dislocation[J/OL]. BMJ Case Rep, 2013 [2022-03-26]. https://casereports.bmj.com/content/2013/bcr-2012-007712.
[7]
Alves OL, Pereira L, Kim SH, et al. Upper Cervical Spine Trauma: WFNS Spine Committee Recommendations[J]. Neurospine, 2020, 17(4): 723-736. DOI: 10.14245/ns.2040226.113.
[8]
Ravikanth R, Majumdar P. Embryological considerations and evaluation of congenital anomalies of craniovertebral junction: A single-center experience[J]. Tzu Chi Med J, 2021, 33(2): 175-180. DOI: 10.4103/tcmj.tcmj_62_20.

PREV Spontaneous basilar artery dissection: One case report
NEXT Clinical features and CMR imaging findings of myocarditis induced by dermatomyositis:One case report
  



Tel & Fax: +8610-67113815    E-mail: editor@cjmri.cn