Dini Leandro I, Mendonça Rodrigo, Adamy Carlos A, Saraiva Glauco A
Department of Neurosurgery, Hospital Centenário, São Leopoldo, Brazil.
Neurosurgery. 2006 Aug;59(2):E426; discussion E426. doi: 10.1227/01.NEU.0000223497.06588.4A.
We report a patient with a cervicothoracic spinal and a mandibular adamantinoma. Adamantinoma is a rare malignant neoplasm of bone and, to our knowledge, there have been only five cases of spinal adamantinoma reported. The pathogenesis of the adamantinoma, as well as the management of this extremely rare spinal tumor, is reviewed.
A 55-year-old man was admitted to our service with cervical pain and signs of C8 and T1 radiculopathy. On physical examination, cervical spine deformity, swelling in the left mandible region, and signs of C8 and T1 radiculopathy were observed. Neuroradiology examinations showed an osteolytic mass of the C6, C7, and T1 vertebral bodies, extending into the lateral masses and transverse processes. After surgical procedures, the patient had clinical improvement.
Corpectomy of C6, C7, and T1 was performed through a cervicothoracic anterior approach. Anterior stabilization of the spine was obtained using an autologous iliac crest graft and osteosynthesis with an anterior plate. On a second procedure, posterior tumor resection and spinal stabilization were performed. After the 1-year follow-up examination, a new anterior procedure was performed because of tumor recidivity and spine instability.
Adamantinoma, an extremely rare lesion, is a locally aggressive tumor with slow growth and the potential to metastasize. Although it is an extremely rare occurrence in the spine, adamantinoma should be considered on the diagnosis of tumors of the vertebrae. Neuroradiological examinations are not specific in the differentiation of this tumor from other conditions. This fact, coupled with the limited experience that most physicians in general have in dealing with this tumor, makes the diagnosis and treatment of adamantinoma challenging.
我们报告一例患有颈胸段脊柱及下颌骨造釉细胞瘤的患者。造釉细胞瘤是一种罕见的骨恶性肿瘤,据我们所知,仅报告过5例脊柱造釉细胞瘤病例。本文对造釉细胞瘤的发病机制以及这种极为罕见的脊柱肿瘤的治疗进行了综述。
一名55岁男性因颈部疼痛及C8和T1神经根病体征入院。体格检查发现颈椎畸形、左下颌骨区域肿胀以及C8和T1神经根病体征。神经放射学检查显示C6、C7和T1椎体有溶骨性肿块,延伸至侧块和横突。手术后,患者临床症状改善。
通过颈胸前路入路对C6、C7和T1进行椎体次全切除术。采用自体髂骨移植及前路钢板内固定实现脊柱前路稳定。在第二次手术中,进行了后路肿瘤切除及脊柱稳定术。1年随访检查后因肿瘤复发及脊柱不稳定进行了再次前路手术。
造釉细胞瘤是一种极为罕见的病变,是一种生长缓慢且具有转移潜能的局部侵袭性肿瘤。尽管其在脊柱中极为罕见,但在诊断椎体肿瘤时应考虑到造釉细胞瘤。神经放射学检查在鉴别该肿瘤与其他疾病时并不具有特异性。这一事实,再加上大多数医生处理这种肿瘤的经验有限,使得造釉细胞瘤的诊断和治疗具有挑战性。