Suppr超能文献

第一颈椎后弓完全缺如:病例报告

Complete absence of the posterior arch of C1: Case report.

作者信息

Khanna R, Smith Z A, Dlouhy B J, Dahdaleh N S

机构信息

Department of Neurological Surgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States.

Department of Neurological Surgery, Washington University, St. Louis, Missouri, United States.

出版信息

J Craniovertebr Junction Spine. 2014 Oct;5(4):176-8. doi: 10.4103/0974-8237.147090.

Abstract

Posterior atlas arch anomalies are relatively common, but have a variety of presentations ranging from partial clefts to complete agenesis of the posterior arch. Partial clefts are prevalent in 4% of patients and are generally asymptomatic. However, complete agenesis of the posterior arch is extremely rare. We report the case of a 46-year-old man who presented with upper cervical spine and occipital pain as well as left sided headaches. Imaging revealed congenital complete absence of the posterior arch of C1 (Type E) without any radiographic evidence of instability. We discuss our case in light of other reported cases and detail its management.

摘要

寰椎后弓异常相对常见,但表现形式多样,从部分裂缺到后弓完全缺如。部分裂缺在4%的患者中较为普遍,通常无症状。然而,后弓完全缺如极为罕见。我们报告一例46岁男性患者,其表现为上颈椎和枕部疼痛以及左侧头痛。影像学检查显示C1后弓先天性完全缺如(E型),无任何影像学不稳定证据。我们结合其他报道的病例讨论该病例,并详述其治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cd1/4279283/c750fcbfba64/JCVJS-5-176-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验