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Intradural Extramedullary Spinal Cord Tumors: A Retrospective Study of Tumor Types, Locations, and Surgical Outcomes

机译:硬膜外髓外脊髓肿瘤:肿瘤类型,位置和手术结果的回顾性研究。

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Introduction: Intradural extramedullary spinal cord tumors (IESCT) account for approximately two thirds of all intraspinal neoplasms. The purpose of this report was to determine short- and long-term outcomes of surgical patients with IESCT, and to examine clinical features that could be helpful in management of patients with these lesions. Methods: A retrospective review of 67 operative IESCT cases between 1974 and 2001 was performed. Outcomes were scored at one month and at mean follow-up of 8.5 months postoperatively. In addition, patient demographics, tumor types and locations were also collected. Statistical analysis was conducted utilizing Chi-square and Student's t-tests. Results: There were 31 men and 36 women (mean age 48 y/o, range 18-87 y/o). Men presented at a younger age than women (44 vs 53 y/o, P<0.02). Fifty-seven (85%) patients presented with severe radiculopathy and/or myelopathy. The remaining 10 (15%) had symptoms typical of disc herniation. Mean duration of symptoms prior to diagnosis was 11 months. Schwannomas (36 patients) had the longest mean duration of symptoms (14.9 months), followed by meningiomas (21 patients, 8.4 months), and ependymomas (10 patients, 2 months). Sixty-three (94%) of patients demonstrated significant improvement at one-month and 62 (92%) at 8.5-month mean follow-up as compared to the index exam. Only 13/67 (19.4%) patients had residual focal deficits on long term follow-up. Conclusions: Surgery for IESCT should be expected to produce significant and dramatic improvement in great majority of patients. Demographic, tumor-specific and anatomic considerations may be clinically useful when approaching IESCT. Introduction Spinal tumors account for only approximately 5-15% of the nervous system neoplasms (1, 2). Intradural extramedullary spinal cord tumors (IESCT) constitute approximately two thirds of these tumors (2, 3). Relatively few published reports have sufficient sample sizes to adequately analyze surgical outcomes, demographics, symptoms, and data on tumor types and locations (3,4,5,6). The most commonly encountered types of IESCT are schwannomas and meningiomas, with myxopapillary ependymomas encountered less frequently. The primary objective of this study was to examine surgical outcomes following procedures for IESCT in a large retrospective cohort of patients. Secondary goals included examination of clinical data pertaining to demographics, symptoms, tumor location and type that could be helpful in clinical decision making. Materials and Methods This is a retrospective study of 67 surgical patients who underwent operative removal of IESCT between September 1974 and May 2001. Parameters recorded include patient demographics, symptoms (severity and duration), tumor characteristics (anatomic and pathologic), postoperative follow-up and surgical outcomes. Surgical intervention was indicated by a combination of presenting symptoms (radiculopathy and/or myelopathy) and radiographic findings of magnetic resonance imaging (MRI), and computed tomographic (CT)-myelography. The neuroimaging procedure of choice was contrast-enhanced MRI. CT-myelography was used in selected patients. Angiography was helpful in cervical dumbbell-shaped lesions. Patient charts were reviewed by one of the authors (SPS or JJG) and pertinent chart data was recorded in a computerized database (Microsoft Excel, Redmond, WA, USA). Surgical outcomes were scored at 1 month and then at the mean follow-up period. The mean follow-up was calculated from the interval between surgery and the last complete clinical examination in the patient chart (in this study, 8.5 months). Patient records were carefully reviewed and surgical outcomes were scored strictly according to the modified criteria of Odom, et al (Table 1) (7). While recognizing the shortcomings of the Odom's criteria as a ‘rough' outcome and morbidity assessment scale, we chose to use this method because of the uniform and standardized recording of these criteri
机译:简介:硬膜外髓外脊髓肿瘤(IESCT)约占所有椎管内肿瘤的三分之二。本报告的目的是确定IESCT外科手术患者的短期和长期结局,并检查有助于治疗这些病变患者的临床特征。方法:回顾性分析1974年至2001年间67例IESCT手术病例。在术后1个月和平均8.5个月的平均随访中对结果进行评分。此外,还收集了患者的人口统计资料,肿瘤类型和位置。使用卡方检验和学生t检验进行统计分析。结果:男31例,女36例(平均年龄48岁,年龄18-87岁)。男性比女性年轻(44 vs 53岁,P <0.02)。五十七(85%)名患者患有严重的神经根病和/或脊髓病。其余10名(15%)患有典型的椎间盘突出症状。诊断前平均症状持续时间为11个月。神经鞘瘤(36例)的平均症状持续时间最长(14.9个月),其次是脑膜瘤(21例,8.4个月)和室间隔瘤(10例,2个月)。与指数检查相比,有63名(94%)的患者在一个月的平均随访中表现出显着改善,在8.5个月的平均随访中有62个(92%)表现出显着改善。在长期随访中,只有13/67(19.4%)的患者残留病灶不足。结论:IESCT手术有望在绝大多数患者中产生显着而显着的改善。在接近IESCT时,人口统计学,肿瘤特异性和解剖学考虑可能在临床上有用。简介脊柱肿瘤仅约占神经系统肿瘤的5-15%(1、2)。硬膜外髓外脊髓肿瘤(IESCT)约占这些肿瘤的三分之二(2、3)。相对而言,很少有已发表的报告具有足够的样本量来充分分析手术结果,人口统计学,症状以及有关肿瘤类型和位置的数据(3、4、5、6)。 IESCT最常见的类型是神经鞘瘤和脑膜瘤,黏膜乳头状室膜膜瘤的发病频率较低。这项研究的主要目的是在一大批回顾性患者队列中检查IESCT手术后的手术结局。次要目标包括检查与人口统计学,症状,肿瘤位置和类型有关的临床数据,这些数据可能有助于临床决策。材料和方法这是一项对1974年9月至2001年5月间手术切除IESCT的67例手术患者的回顾性研究。记录的参数包括患者的人口统计学,症状(严重程度和持续时间),肿瘤特征(解剖学和病理学),术后随访和手术结果。出现症状(神经根病和/或脊髓病)和磁共振成像(MRI)和计算机断层扫描(CT)-脊髓造影的影像学表现相结合可指示手术干预。选择的神经影像学检查方法是造影剂增强MRI。在选定的患者中使用了CT脊髓造影。血管造影有助于宫颈哑铃状病变。由一位作者(SPS或JJG)审查了患者病历,并将相关病历数据记录在计算机数据库(Microsoft Excel,美国华盛顿州雷德蒙德)中。分别在1个月和平均随访期间对手术结果进行评分。根据患者图表中手术与最后一次完整临床检查之间的时间间隔(在本研究中为8.5个月)计算平均随访时间。认真审查患者记录,并严格按照Odom等人的修改标准对手术结果进行评分(表1)(7)。在将Odom标准的缺点识别为“粗糙”的结果和发病率评估量表的同时,我们选择使用此方法,因为这些标准的记录是统一和标准化的

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