Du Kaili, Lou Zhenkai, Zhang Chunqiang, Guo Peiyu, Chen Lingqiang, Wang Bing, Huang Dongsheng
Department of Orthopedics, the First Affiliated Hospital, Kunming Medical University, Kunming, China.
Department of Orthopedics, the First Affiliated Hospital, Kunming Medical University, Kunming, China.
World Neurosurg. 2018 Mar;111:94-98. doi: 10.1016/j.wneu.2017.12.054. Epub 2017 Dec 16.
Spinal osteochondroma is a rare but recognized cause of myelopathy. Brown-Séquard syndrome is a form of severe myelopathy characterized by a clinical picture of hemisection of the spinal cord. Brown-Séquard syndrome caused by osteochondroma is extremely rare, calling for individualized surgical procedures.
We report a 16-year-old girl with hereditary multiple exostoses and a rare case of thoracic osteochondroma causing partial Brown-Séquard syndrome. Customized surgical procedures were designed to avoid iatrogenic spinal cord injury. The patient underwent neural decompression and tumor excision through a transpedicular approach. The surgical procedure consisted of 4 consecutive steps: 1) laminectomy, 2) costotransversectomy and pediculectomy, 3) extracavitary removal of the mass, and 4) pedicular fixation with fusion. Total resection of the tumor was achieved macroscopically without intraoperative spinal cord injury. The postoperative recovery was uneventful, and the patient returned to a normal life without evidence of recurrence at 24-month follow-up.
For patients with hereditary multiple exostosis and new onset of neurologic symptoms, the possibility of a spinal osteochondroma should be considered. In the situation of an intraspinal exostosis protruding from the lateral side, customized surgical procedures with a transpedicular approach may be a valid way to minimize intraoperative neural injury and achieve a satisfactory outcome.
脊柱骨软骨瘤是一种罕见但已被认可的脊髓病病因。布朗 - 塞卡尔综合征是一种严重脊髓病的形式,其特征为脊髓半切的临床表现。由骨软骨瘤引起的布朗 - 塞卡尔综合征极为罕见,需要个体化的手术方法。
我们报告一名16岁患有遗传性多发性骨软骨瘤的女孩,以及一例罕见的胸椎骨软骨瘤导致部分布朗 - 塞卡尔综合征的病例。设计了定制的手术方法以避免医源性脊髓损伤。患者通过经椎弓根入路接受了神经减压和肿瘤切除。手术过程包括连续4个步骤:1)椎板切除术,2)肋横突切除术和椎弓根切除术,3)肿块的腔外切除,4)椎弓根固定融合。肿瘤在肉眼下实现了全切,术中无脊髓损伤。术后恢复顺利,患者恢复正常生活,24个月随访时无复发迹象。
对于患有遗传性多发性骨软骨瘤且新出现神经症状的患者,应考虑脊柱骨软骨瘤的可能性。在椎管内骨软骨瘤从侧面突出的情况下,采用经椎弓根入路的定制手术方法可能是将术中神经损伤降至最低并取得满意结果的有效方法。