Raj Aditya, Srivastava Sudhir Kumar, Marathe Nandan, Bhosale Sunil, Purohit Shaligram
Department of Orthopaedics, Seth GS Medical College and KEM Hospital, Parel, Mumbai, Maharashtra, India.
Asian J Neurosurg. 2020 Feb 25;15(1):236-240. doi: 10.4103/ajns.AJNS_35_19. eCollection 2020 Jan-Mar.
Os odontoideum (OO) was first described by Giacomini in 1886 as separation of the odontoid process from the body of the axis. Instability can consequently occurs at this level due to the failure of the transverse atlantal ligament (TAL) and this atlantoaxial instability can be a cause of progressive neurological deficits. It is considered a rare anomaly of the odontoid process. It is a disease with controversial etiology, debatable incidence, and only a partly known natural history owing to the paucity of the literature on this topic. There are insufficient demographic data about the occurrence of the disease, and most of the management is dictated by the isolated case reports and few studies which have been carried out at handful of institutes. OO is classified into two types by Fielding . based on the anatomic location: orthotopic and dystopic. Orthotopic OO consists of an ossicle that moves with the anterior arch of the atlas, whereas the dystopic type presents as an ossicle near the basion or one that is fused with the clivus. In one magnetic resonance imaging (MRI) study of odontoid morphology, a 0.7% (1 case of 133 patients) incidence was reported. The spectrum of the clinical presentation varies from completely asymptomatic individuals to patients presenting with features of cervical myelopathy. Here, we present a case of 35-year-old-male with dystopic OO who presented to us with features of gradually progressing cervical myelopathy without any obvious history of neck trauma. On investigations, he was found to have atlantoaxial instability with wide atlanto-dens interval. He was treated with the posterior C1-C2 stabilization and reduction of atlantoaxial instability.
齿突骨(OO)于1886年由贾科米尼首次描述为齿突与枢椎体分离。由于寰椎横韧带(TAL)功能失效,该水平可能会出现不稳定,这种寰枢椎不稳定可能是进行性神经功能缺损的一个原因。它被认为是一种罕见的齿突异常。这是一种病因存在争议、发病率有争议且由于关于该主题的文献匮乏其自然史仅部分为人所知的疾病。关于该疾病发生情况的人口统计学数据不足,并且大多数治疗方法是由个别病例报告以及少数在少数机构进行的研究所决定的。根据解剖位置,菲尔德将OO分为两种类型:原位型和异位型。原位型OO由一块与寰椎前弓一起移动的小骨组成,而异位型则表现为靠近颅底的小骨或与斜坡融合的小骨。在一项关于齿突形态的磁共振成像(MRI)研究中,报告的发病率为0.7%(133例患者中有1例)。临床表现的范围从完全无症状的个体到表现为颈椎病特征的患者。在此,我们报告一例35岁男性异位型OO患者,他因逐渐进展的颈椎病特征前来就诊,无明显颈部外伤史。经检查,发现他存在寰枢椎不稳定,寰齿间距增宽。他接受了后路C1 - C2固定及寰枢椎不稳定复位治疗。