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寰椎发育不全与寰椎横韧带骨化:一种导致颈椎病的罕见原因。

Atlas hypoplasia and ossification of the transverse atlantal ligament: a rare cause of cervical myelopathy.

作者信息

Bokhari Rakan, Baeesa Saleh

机构信息

Division of Neurological Surgery, College of Medicine, King Abdulaziz University, P.O. Box 80215, Jeddah 21589, Saudi Arabia.

出版信息

Case Rep Neurol Med. 2012;2012:893284. doi: 10.1155/2012/893284. Epub 2012 Dec 5.

Abstract

Myelopathy at the level of the atlas is rarely encountered by the practicing spine surgeon. Due to the region's unique anatomy, compression of the cord at this level is either caused by a large compressing lesion or an abnormally stenotic canal. We describe a rare instance of a congenitally stenotic canal due to a hypoplastic intact posterior arch of atlas, coexisting with an extremely rare ossified transverse ligament of the atlas. The coexistence of these two lesions has only been documented thrice before. We describe the clinical presentation, imaging findings, and favorable response to surgery.

摘要

寰椎水平的脊髓病在脊柱外科医生的实际工作中很少遇到。由于该区域独特的解剖结构,此水平的脊髓受压要么是由大的压迫性病变引起,要么是由异常狭窄的椎管所致。我们描述了一例罕见的因寰椎后弓发育不全但完整而导致的先天性椎管狭窄病例,同时并存极其罕见的寰椎横韧带骨化。这两种病变的并存此前仅有三次文献记载。我们描述了其临床表现、影像学表现以及对手术的良好反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac4e/3529449/14e3272b75bf/CRIM.NM2012-893284.001.jpg

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