Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan; Department of Orthopaedic Surgery, Kyushu University Beppu Hospital, Oita, Japan.
Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
J Orthop Sci. 2022 May;27(3):563-568. doi: 10.1016/j.jos.2021.02.014. Epub 2021 Apr 23.
Multiple spinal cord tumors in a single patient are very rare and most often seen in cases of neurofibromatosis and associated disorders. Schwannomatosis, which is characterized by the development of multiple schwannomas without vestibular schwannomas, has been newly defined as a distinct form of neurofibromatosis. The purpose of the present study was to describe and review the clinical and radiological features and the management of patients with multiple spinal schwannomas without vestibular schwannomas.
Between 1986 and 2016, 19 patients with multiple spinal schwannomas without vestibular schwannoma were diagnosed and treated. Of the 19 patients, 13 were males, and 6 were females. The mean age at the first surgery for spinal schwannoma was 45.2 years old. The mean follow-up period was 123.4 months. The clinical features and radiological findings of the patients with multiple spinal schwannomas were retrospectively reviewed.
Among the 19 patients, there were more than 140 spinal schwannomas. The most common area of spinal schwannoma was the thoracolumbar-lumbar region. Initial symptoms and chief complaints caused by spinal schwannomas were primarily pain in the trunk or extremities in 17 (89.5%) of 19 patients. More than 60 spinal schwannomas were surgically resected. Multiple spinal surgeries were required in six patients. In all 19 patients, surgical treatment has provided successful relief of symptoms and neurological recovery.
Surgical treatment was safe and effective in patients with multiple spinal schwannomas without vestibular schwannomas. After surgery, we recommend that all patients be followed with magnetic resonance imaging to monitor for asymptomatic tumors or detect new tumors early.
单个患者中出现多个脊髓肿瘤非常罕见,最常见于神经纤维瘤病及相关疾病。而由多个许旺细胞瘤(无前庭神经鞘瘤)组成的神经鞘瘤病,已被新定义为一种独特的神经纤维瘤病形式。本研究旨在描述和回顾无前庭神经鞘瘤的多发性脊髓神经鞘瘤患者的临床和影像学特征及治疗方法。
1986 年至 2016 年间,共诊断并治疗了 19 例无前庭神经鞘瘤的多发性脊髓神经鞘瘤患者。19 例患者中,男性 13 例,女性 6 例。首次行脊髓神经鞘瘤手术时的平均年龄为 45.2 岁。平均随访时间为 123.4 个月。回顾性分析了多发性脊髓神经鞘瘤患者的临床特征和影像学表现。
19 例患者中共有 140 多个脊髓神经鞘瘤。最常见的脊髓神经鞘瘤发生部位是胸腰椎-腰骶部。19 例患者中,17 例(89.5%)最初的症状和主要主诉是躯干或四肢疼痛。超过 60 个脊髓神经鞘瘤被手术切除。6 例患者需要多次进行脊髓手术。19 例患者均接受了手术治疗,均成功缓解了症状和恢复了神经功能。
对于无前庭神经鞘瘤的多发性脊髓神经鞘瘤患者,手术治疗安全有效。手术后,我们建议所有患者都要进行磁共振成像随访,以监测无症状肿瘤或早期发现新肿瘤。