Zeoli Tyler, Iwanaga Joe, Bui C J, Dumont Aaron S, Tubbs R Shane
Department of Neurosurgery, Tulane Center for Clinical Neurosciences, Tulane University School of Medicine, New Orleans, LA, USA.
Department of Neurology, Tulane Center for Clinical Neurosciences, Tulane University School of Medicine, New Orleans, LA, USA.
Anat Cell Biol. 2020 Dec 31;53(4):522-526. doi: 10.5115/acb.20.189.
Duplication of the odontoid process remains a rare developmental pathology that is underrepresented in the current literature. As the pivot point for the craniovertebral junction, the odontoid process is vital for the integrity of the atlanto-axial joint and the ability of the head and cervical spine to rotate correctly. The pathogenesis being incompletely understood, it has been proposed that odontoid process duplication involves faulty sclerotome migration and disruption of the axis ossification center. Patients presenting with this pathology usually have associated structural abnormalities. A detailed anatomical and embryological understanding of the odontoid process is necessary for successful management and treatment of patients presenting with odontoid process duplication. We present a rare case of a patient with a duplicated odontoid process in association with C2-C3 fusion, incomplete anterior arch of C1, variant inferior bony process of the transverse process of C1, and enlarged right jugular foramen.
齿突重复仍然是一种罕见的发育性病理情况,在当前文献中报道较少。作为颅颈交界的枢轴点,齿突对于寰枢关节的完整性以及头部和颈椎正确旋转的能力至关重要。由于其发病机制尚未完全明确,有人提出齿突重复涉及硬骨节迁移异常和枢椎骨化中心的破坏。患有这种病理情况的患者通常伴有相关的结构异常。对于成功管理和治疗齿突重复的患者,对齿突进行详细的解剖学和胚胎学了解是必要的。我们报告了一例罕见病例,该患者存在齿突重复,并伴有C2-C3融合、C1前弓不完整、C1横突下骨性突起变异以及右侧颈静脉孔扩大。