Nakamura Masaya, Iwanami Akio, Tsuji Osahiko, Hosogane Naobumi, Watanabe Kota, Tsuji Takashi, Ishii Ken, Toyama Yoshiaki, Chiba Kazuhiro, Matsumoto Morio
Department of Orthopaedic Surgery, School of Medicine, Keio University, 35 Shinanomachi, Shinjuku, Tokyo 160-8582, Japan.
J Orthop Sci. 2013 Jan;18(1):8-13. doi: 10.1007/s00776-012-0300-2. Epub 2012 Sep 5.
Retrospective case series.
To evaluate our treatment strategy for cervical dumbbell neurinoma. In treating cervical dumbbell neurinoma, possible difficulties include reoperation due to recurrent tumor, denervation due to nerve root resection, and postoperative spinal deformity due to extensive bony removal.
We reviewed 75 cases of cervical dumbbell neurinoma that were treated surgically between 1985 and 2006. Postoperative neurological deficits, effects of surgical margins on tumor recurrence, and surgical complications were investigated retrospectively.
Sensory and motor deficits due to resection of specific nerve roots appeared temporarily in 33 and 23 % of all cases, and persisted in 8 and 8 % at final evaluation, respectively. Total, subtotal, and partial resection was performed in 57, 13, and 5 cases, respectively. The total resection rate was low in the tumors that had large extraforaminal components. Of the subtotally resected 13 cases, only two cases of high tumor-growth rate required re-operation or showed tumor growth. Among the five partially resected cases, re-operation was necessary in two cases 13 and 15 years later because of aggravated neurological symptoms due to tumor growth. Two patients who underwent C2 laminectomy developed kyphosis, and three patients who underwent facet joint resection and curettage of vertebral body lesions developed scoliosis.
Total resection should be attempted for cervical dumbbell tumors. In cases where total resection was potentially of high risk, however, subtotal resection (within the capsule) was found to be a practical choice yielding favorable long-term outcome when the tumor growth rate (MIB-1 index) was low.
回顾性病例系列研究。
评估我们对颈椎哑铃形神经鞘瘤的治疗策略。在治疗颈椎哑铃形神经鞘瘤时,可能遇到的困难包括因肿瘤复发而再次手术、因神经根切除导致神经支配丧失以及因广泛的骨质切除导致术后脊柱畸形。
我们回顾了1985年至2006年间接受手术治疗的75例颈椎哑铃形神经鞘瘤病例。回顾性调查术后神经功能缺损、手术切缘对肿瘤复发的影响以及手术并发症。
在所有病例中,分别有33%和23%的患者因特定神经根切除出现暂时的感觉和运动功能缺损,最终评估时分别有8%和8%的患者仍存在这些缺损。分别有57例、13例和5例患者进行了全切除、次全切除和部分切除。对于有较大椎间孔外成分的肿瘤,全切除率较低。在13例次全切除的病例中,只有2例肿瘤生长速度快的患者需要再次手术或出现肿瘤生长。在5例部分切除的病例中,有2例分别在13年和15年后因肿瘤生长导致神经症状加重而需要再次手术。2例行C2椎板切除术的患者出现后凸畸形,3例行小关节切除及椎体病变刮除术的患者出现脊柱侧凸。
对于颈椎哑铃形肿瘤应尝试进行全切除。然而,在全切除存在高风险的情况下,当肿瘤生长速度(MIB-1指数)较低时,次全切除(包膜内)是一种可行的选择,可获得良好的长期效果。