Stability and motion: addressing the pathology of Chiari malformation and craniocervical junction

被引:0
|
作者
Limbrick, David D., Jr. [1 ]
Brockmeyer, Douglas L. [2 ]
Goel, Atul [3 ]
Strahle, Jennifer M. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Neurol Surg, St Louis, MO 63110 USA
[2] Univ Utah, Dept Neurosurg, Salt Lake City, UT USA
[3] Lilavati Hosp & Res Ctr, Dept Neurosurg, Mumbai, Maharashtra, India
关键词
D O I
10.3171/2022.12.FOCUS22636
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
P hysiology of the craniocervical/cervicomedullary region requires at once stability and motion. Alterations in biomechanical and hydrodynamic properties may result in central nervous system pathology with profound impact on neurological function and quality of life. Chiari type I malformation, syringomyelia, and basilar invagination, for example, are discrete clinical entities that frequently occur as a cohort and may be relentlessly progressive. In recent years, advances in dynamic high-resolution imaging and detailed phenotyping, coupled with surgical innovation and aggregated clinical experience, have enabled substantial advances in the treatment of these conditions. © AANS 2023, except where prohibited by US copyright law
引用
收藏
页数:1
相关论文
共 50 条
  • [41] Craniometric Analysis of the Hindbrain and Craniocervical Junction of Chihuahua, Affenpinscher and Cavalier King Charles Spaniel Dogs With and Without Syringomyelia Secondary to Chiari-Like Malformation
    Knowler, Susan P.
    Kiviranta, Anna-Mariam
    McFadyen, Angus K.
    Jokinen, Tarja S.
    La Ragione, Roberto M.
    Rusbridge, Clare
    PLOS ONE, 2017, 12 (01):
  • [42] Are craniocervical angulations or syrinx risk factors for the initiation and progression of scoliosis in Chiari malformation type I?
    Luo, Ming
    Wu, Diwei
    You, Xuanhe
    Deng, Zhipeng
    Liu, Limin
    Song, Yueming
    Huang, Shishu
    NEUROSURGICAL REVIEW, 2021, 44 (04) : 2299 - 2308
  • [43] Chiari malformation Type 1 and atlantoaxial instability: a letter from the Pediatric Craniocervical Society Response
    Goel, Atul
    JOURNAL OF NEUROSURGERY-SPINE, 2015, 23 (06) : 821 - 823
  • [44] Cystic angiomatosis of the craniocervical junction associated with Chiari I malformationCase report and review of the literature
    Marco Pavanello
    Gianluca Piatelli
    Marcello Ravegnani
    Alessandro Consales
    Andrea Rossi
    Paolo Nozza
    Claudia Milanaccio
    Marco Carbone
    Armando Cama
    Child's Nervous System, 2007, 23 : 697 - 700
  • [45] Morphometric features of the craniocervical junction region in dogs with suspected Chiari-like malformation determined by combined use of magnetic resonance imaging and computed tomography
    Marino, Dominic J.
    Loughin, Catherine A.
    Dewey, Curtis W.
    Marino, Leonard J.
    Sackman, Joseph J.
    Lesser, Martin L.
    Akerman, Meredith B.
    AMERICAN JOURNAL OF VETERINARY RESEARCH, 2012, 73 (01) : 105 - 111
  • [46] Craniocervical decompression with duraplasty and cerebellar tonsillectomy as treatment for Chiari malformation-I complicated with syringomyelia
    Bao, C. S.
    Liu, L.
    Wang, B.
    Xia, X. -G.
    Gu, Y. J.
    Li, D. J.
    Zhan, S. L.
    Chen, G. L.
    Yang, F. B.
    GENETICS AND MOLECULAR RESEARCH, 2015, 14 (01) : 952 - 960
  • [47] Complex Chiari malformation: using craniovertebral junction metrics to guide treatment
    Ho, Winson S. C.
    Brockmeyer, Douglas L.
    CHILDS NERVOUS SYSTEM, 2019, 35 (10) : 1847 - 1851
  • [48] Morphometric analysis of posterior fossa and craniovertebral junction in subtypes of Chiari malformation
    Basaran, Recep
    Efendioglu, Mustafa
    Senol, Mehmet
    Ozdogan, Selcuk
    Isik, Nejat
    CLINICAL NEUROLOGY AND NEUROSURGERY, 2018, 169 : 1 - 11
  • [49] Complex Chiari malformation: using craniovertebral junction metrics to guide treatment
    Winson S.C. Ho
    Douglas L. Brockmeyer
    Child's Nervous System, 2019, 35 : 1847 - 1851
  • [50] Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Mobius syndrome
    Al Kaissi, Ali
    Grill, Franz
    Safi, Hatem
    Ben Ghachem, Maher
    Ben Chehida, Farid
    Klaushofer, Klaus
    ORPHANET JOURNAL OF RARE DISEASES, 2007, 2 (1)