Embryology and bony malformations of the craniovertebral junction

被引:166
作者
Pang, Dachling [1 ,2 ,3 ]
Thompson, Dominic N. P. [4 ]
机构
[1] Kaiser Permanente Med Ctr, Dept Paediat Neurosurg, Oakland, CA 94611 USA
[2] Univ Calif Davis, Dept Neurol Surg, Sacramento, CA 95817 USA
[3] Kaiser Fdn Hosp No Calif, Reg Ctr Pediat Neurosurg, Oakland, CA USA
[4] Great Ormond St Hosp Sick Children, Dept Paediat Neurosurg, London WC1N 3JH, England
关键词
Craniovertebral junction; Congenital malformations; Genetic control; Occipital-cervical instability; Cord compression; Occipital-cervical fusion; Primary somitogenesis; Sclerotomal resegmentation; Embryology; Malformation; Surgery; OS-ODONTOIDEUM; SEGMENTATION CLOCK; GENE-EXPRESSION; POSTERIOR ARCH; I MALFORMATION; SOMITE CELLS; PAX GENE; ANOMALIES; ATLAS; ABNORMALITIES;
D O I
10.1007/s00381-010-1358-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The embryology of the bony craniovertebral junction (CVJ) is reviewed with the purpose of explaining the genesis and unusual configurations of the numerous congenital malformations in this region. Functionally, the bony CVJ can be divided into a central pillar consisting of the basiocciput and dental pivot and a two-tiered ring revolving round the central pivot, comprising the foramen magnum rim and occipital condyles above and the atlantal ring below. Embryologically, the central pillar and the surrounding rings descend from different primordia, and accordingly, developmental anomalies at the CVJ can also be segregated into those affecting the central pillar and those affecting the surrounding rings, respectively. A logical classification of this seemingly unwieldy group of malformations is thus possible based on their ontogenetic lineage, morbid anatomy, and clinical relevance. Representative examples of the main constituents of this classification scheme are given, and their surgical treatments are selectively discussed.
引用
收藏
页码:523 / 564
页数:42
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