Celli Paolo
Division of Neurosurgery, Department of Neurological Sciences, Second Faculty of Medicine, La Sapienza University, Rome, Italy.
Neurosurgery. 2002 Sep;51(3):684-92; discussion 692.
Surgery for the treatment of patients with spinal nerve sheath tumors can require complete resection of the nerve roots involved in the tumor. The purpose of the present study is to analyze the risks of resection of eloquent roots as compared with the risks of incomplete tumor removal.
The pertinent literature on spinal nerve sheath tumors was reviewed. A single-institution series of 26 patients who underwent operations for 27 spinal schwannomas or neurofibromas, which were removed together with functionally relevant nerve roots (C5-C8 or L3-S1), was studied.
Worsening of preoperative radicular motor function was observed at follow-up in 4 (14.8%) of the 27 divided nerve roots, but the motor deficit was permanent and disabling in only 2 cases (7.4%). In the four patients who experienced worsened radicular motor function, the roots were cervical, and histological analysis revealed that the tumor was a schwannoma. Three of these patients were neurologically negative before surgery. Of the two patients with severe radicular weakness, the location of the tumor was extradural and extraradicular in one patient, who had normal preoperative root function, and the tumor was intraextradural in the other patient, who had a preoperative root deficit.
After resection of a single eloquent nerve root involved in a nerve sheath tumor, the incidence of radicular dysfunction is low but severe weakness is possible. The main risk factors seem to be the pathological pattern (schwannoma versus neurofibroma) of tumor, the preoperative status (with versus without deficit) of the root, and, for extradural nerve sheath tumors, the location (cervical and extraradicular versus lumbosacral and intraradicular) of growth. Deafferentation pain does not occur. Unlike schwannomas with neurofibromatosis Type 2 and neurofibromas, the radicality of removal seems to be the main factor with regard to the recurrence of solitary schwannomas, although recurrent tumors often appear later in follow-up.
手术治疗脊神经鞘瘤患者可能需要完全切除肿瘤累及的神经根。本研究的目的是分析切除明确功能的神经根的风险与不完全切除肿瘤的风险。
回顾了有关脊神经鞘瘤的相关文献。研究了一个单机构系列的26例患者,他们接受了27例脊髓神经鞘瘤或神经纤维瘤的手术,这些肿瘤与功能相关的神经根(C5 - C8或L3 - S1)一起被切除。
在随访中,27条被切断的神经根中有4条(14.8%)出现术前神经根运动功能恶化,但仅2例(7.4%)的运动功能缺损是永久性且致残的。在4例神经根运动功能恶化的患者中,神经根为颈部,组织学分析显示肿瘤为神经鞘瘤。其中3例患者术前神经功能正常。在2例严重神经根无力的患者中,1例患者肿瘤位于硬膜外和神经根外,术前神经根功能正常,另1例患者肿瘤位于硬膜内外,术前有神经根功能缺损。
切除神经鞘瘤累及的单条明确功能的神经根后,神经根功能障碍的发生率较低,但仍可能出现严重无力。主要危险因素似乎是肿瘤的病理类型(神经鞘瘤与神经纤维瘤)、神经根的术前状态(有或无功能缺损),以及对于硬膜外神经鞘瘤,生长部位(颈部和神经根外与腰骶部和神经根内)。不会发生去传入性疼痛。与2型神经纤维瘤病的神经鞘瘤和神经纤维瘤不同,对于孤立性神经鞘瘤的复发,切除的彻底性似乎是主要因素,尽管复发性肿瘤常在随访后期出现。