先天性寰椎后弓发育不全伴颈髓内高强度病变1例报告。

IF 0.4 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2025-04-22 eCollection Date: 2025-04-01 DOI:10.1093/jscr/rjae689
Jian Zhang, Jiahao Liu, Jingyu Jia, Xinxin Miao, Xigao Cheng
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引用次数: 0

摘要

先天性寰椎后弓发育不全是一种罕见且无典型症状的疾病。一名49岁女性,有2年复发性眩晕发作史。入院前1个月,患者开始双下肢无力,行走不稳,行走后胸闷、气短。她没有任何外伤史。颈椎影像学显示C1后弓部分发育不全,前弓中线裂,颈椎高强度髓内病变。我们采用后路枕下中线入路切除C1后弓。该病例强调了鉴别诊断的重要性,应进行详细的影像学检查以正确评估寰枢椎的稳定性。对于有神经系统症状但没有严重脊髓压迫的患者,孤立的后弓应被认为是症状的潜在原因,后弓切除术是有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital hypoplasia of the posterior arch of the atlas accompanied with cervical high-intensity intramedullary lesions: a case report.

Congenital hypoplasia of the posterior arch of the atlas (C1) is uncommon and typically asymptomatic. A 49-year-old woman presented with a 2-year history of recurrent vertigo attacks. One month before admission, she began to have weakness in both lower extremities and unsteady walking, with chest tightness and shortness of breath after walking. She did not have any history of trauma. Cervical spine imaging revealed partial hypoplasia of the posterior arch of C1, midline cleft of the anterior arch, and cervical high-intensity intramedullary lesions. We used a posterior, suboccipital midline approach to resect the posterior arch of C1. This case underscores the importance of differential diagnosis, detailed imaging examinations should be performed to properly assess the stability of the atlantoaxial spine. In patients with neurological symptoms but no severe spinal cord compression, isolated posterior arch should be considered an potential cause of symptoms, and posterior arch resection is effective.

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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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