Ryu Kyeong-Sik, Lee Ki-Yeol, Lee Hong-Jae, Park Chun-Kun
Neurosurgery Department, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul, Korea.
J Korean Neurosurg Soc. 2011 May;49(5):302-4. doi: 10.3340/jkns.2011.49.5.302. Epub 2011 May 31.
Thoracic intramedullary schwannomas are rare spinal cord tumors. Most of these tumors have been reported as a single lesion in the spinal cord. The authors report the first case of intramedullary schwannoma accompanying by extramedullary beads-like daughter masses of the thoracic spine. A 68-year-old male presented with walking disturbance and decreased sensation below T10 dermatome. Imaging workup revealed an intramedullary mass at T6 and T7. T6 and T7 laminectomy and mass removal were performed. Intraoperatively, extramedullary beads-like daughter masses along the nerve roots adjacent to intramedullary mass were identified. Total removal of intramedullary lesion and partial resection of extramedullary masses were done. Histological analysis confirmed the diagnosis of schwannoma. The patient could ambulate independently at postoperative 1 month without any neurological sequelae. The authors experienced a surgical case of intramedullary schwannoma accompanying by extramedullary beads-like same pathologies in the thoracic spine.
胸段髓内神经鞘瘤是罕见的脊髓肿瘤。大多数此类肿瘤报道为脊髓内单个病灶。作者报告了首例胸段髓内神经鞘瘤伴有髓外串珠样子肿块的病例。一名68岁男性出现行走障碍及T10皮节以下感觉减退。影像学检查显示T6和T7水平有一髓内肿块。行T6和T7椎板切除术及肿块切除术。术中,在与髓内肿块相邻的神经根处发现了髓外串珠样子肿块。髓内病灶全切及髓外肿块部分切除。组织学分析确诊为神经鞘瘤。患者术后1个月可独立行走,无任何神经后遗症。作者经历了一例胸段髓内神经鞘瘤伴有髓外串珠样相同病理改变的手术病例。