Zaijun Lin, Xinhai Yang, Zhipeng Wu, Wending Huang, Quan Huang, Zhenhua Zhou, Dapeng Fen, Jisheng Zhang, Wei Zheng, Jianru Xiao
Orthopaedics Department, Changzhen Hospital, The Second Military Medical University, Shanghai, China.
J Spinal Disord Tech. 2013 Jun;26(4):194-9. doi: 10.1097/BSD.0b013e31823eb239.
A retrospective study of 14 spinal osteochondroma (OC) patients with compressive myelopathy or radiculopathy who underwent excision of the lesions.
To evaluate the surgical results of a series of cases of symptomatic OCs and the risk of recurrence and malignant transformation in the mobile spine.
Intraspinal OC with symptomatic spinal cord or nerve root compression is a rare disease. Most of the lesions require surgical treatment. However, some patients may relapse or malignant transformation may occur after surgery.
Fourteen symptomatic spinal OC cases, including 2 hereditary multiple exostoses, were treated surgically from 2001 to 2010. The clinical history, plain radiographs, computed tomography, magnetic resonance imaging, pathologic characteristics, surgical treatments, and outcomes were reviewed. All the patients were followed up for an average of 48.9 months.
The 14 patients included 8 with lesions in the cervical spine, 3 with lesions in the thoracic spine, and 2 with lesions in the lumbar spine. One patient had a particularly large lesion which extended from C7 to T6. The OCs originated from the lamina (4), lateral mass (3), vertebral body (3), processus transversus (1), spinous process (1), pedicle of vertebral arch (1), and an indeterminate location (1). Six patients presented with myelopathy from spinal cord compression and 8 with radiculopathy from nerve root compression. Operative approaches included posterior (11) and combined posterior anterior (3) patients. The surgical outcome was satisfactory in 79% (11) of patients. Two recurrent lesions were notable for sarcomatous transformation.
We recommend gross total resection of all diagnosed OCs involving the mobile spine because of the risk of malignant transformation. Early detection and total excision of symptomatic spinal lesions in these cases may be the key to providing the best outcome. The neurological defect arising from OC can be improved by surgical intervention in most patients.
对14例因脊髓型或神经根型脊髓压迫症而接受病变切除的脊柱骨软骨瘤(OC)患者进行回顾性研究。
评估一系列有症状的OC病例的手术结果以及活动脊柱中复发和恶变的风险。
伴有脊髓或神经根压迫症状的椎管内OC是一种罕见疾病。大多数病变需要手术治疗。然而,一些患者术后可能复发或发生恶变。
回顾性分析2001年至2010年期间手术治疗的14例有症状的脊柱OC病例,其中包括2例遗传性多发骨软骨瘤。回顾了患者的临床病史、X线平片、计算机断层扫描、磁共振成像、病理特征、手术治疗方法及结果。所有患者平均随访48.9个月。
14例患者中,颈椎病变8例,胸椎病变3例,腰椎病变2例。1例患者病变特别大,从C7延伸至T6。OC起源于椎板(4例)、侧块(3例)、椎体(3例)、横突(1例)、棘突(1例)、椎弓根(1例)及位置不明确处(1例)。6例患者因脊髓受压出现脊髓病,8例因神经根受压出现神经根病。手术入路包括后路(11例)和前后联合入路(3例)。79%(11例)的患者手术效果满意。2例复发病变出现肉瘤样变。
由于存在恶变风险,我们建议对所有诊断为累及活动脊柱的OC进行全切。早期发现并全切这些病例中有症状的脊柱病变可能是获得最佳治疗效果的关键。在大多数患者中,手术干预可改善由OC引起的神经功能缺损。