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后颅窝脑膜瘤的治疗策略及长期预后

Therapeutic strategy and long-term outcome of meningiomas located in the posterior cranial fossa.

作者信息

Matsui Toru

机构信息

Department of Neurosurgery, Saitama Medical Center/Saitama Medical University, Saitama, Japan.

出版信息

Neurol Med Chir (Tokyo). 2012;52(10):704-13. doi: 10.2176/nmc.52.704.

DOI:10.2176/nmc.52.704
PMID:23095262
Abstract

The clinical and surgical findings of 41 consecutive cases of posterior cranial fossa meningiomas operated on between January 1987 and December 2011 at Saitama Medical Center/Saitama Medical University were reviewed. The 31 female and 10 male patients were aged from 19 to 74 years (mean 54 years). The tumors were located in the petroclival (N=15), craniovertebral junction (N=6), lateral tentorial (N=12), and cerebellopontine angle (N=8) regions. Mean tumor equivalent diameter was 4.3 cm (range 2-9 cm). Head pain (46.3%) and gait disturbance (26.8%) were the most common presenting symptoms, and cranial neuropathies were the most common neurological signs on admission. Mean preoperative performance status (Karnofsky scale) was 83% (range 40-100%). Surgical approaches to these tumors included presigmoidal transpetrosal, retrosigmoidal, transcondylar, and combined approaches. In 4 cases, a staged procedure was performed. Gross total resection was achieved in 85.4% of patients, and subtotal/partial resection in 12.2%. Surgical mortality was 2.4% and complications were encountered in 11 patients (26.8%) including temporary neurological deficits in 4 patients. The mean follow-up period was 8.2 years, ranging from 1 to 24 years, and the mean performance status of patients at 12 months after the last surgery was 92% (range 0-100%). Recurrence or progression of disease was found in 9.8% of cases. Postoperative adjuvant therapy was performed in 6 cases. My experience suggests that although posterior cranial fossa meningiomas represent a continuing challenge for contemporary neurosurgeons, such tumors may be completely or subtotally removed with low rate of mortality and acceptable morbidity, allowing most of these patients to achieve good outcome in long-term follow up.

摘要

回顾了1987年1月至2011年12月期间在埼玉医疗中心/埼玉医科大学接受手术的41例连续颅后窝脑膜瘤患者的临床和手术结果。31例女性和10例男性患者年龄在19至74岁之间(平均54岁)。肿瘤位于岩斜区(n = 15)、颅颈交界区(n = 6)、小脑幕外侧(n = 12)和桥小脑角区(n = 8)。肿瘤平均等效直径为4.3 cm(范围2 - 9 cm)。头痛(46.3%)和步态障碍(26.8%)是最常见的首发症状,入院时最常见的神经体征是颅神经病变。术前平均功能状态(卡诺夫斯基量表)为83%(范围40 - 100%)。这些肿瘤的手术入路包括乙状窦前经岩骨、乙状窦后、经髁及联合入路。4例患者进行了分期手术。85.4%的患者实现了肿瘤全切除,12.2%的患者实现了次全/部分切除。手术死亡率为2.4%,11例患者(26.8%)出现并发症,其中4例患者出现暂时性神经功能缺损。平均随访期为8.2年,范围为1至24年,最后一次手术后12个月患者的平均功能状态为92%(范围0 - 100%)。9.8%的病例发现疾病复发或进展。6例患者进行了术后辅助治疗。我的经验表明,尽管颅后窝脑膜瘤对当代神经外科医生来说仍然是一个持续的挑战,但这类肿瘤可以被完全或次全切除,死亡率低且发病率可接受,使大多数患者在长期随访中能取得良好的结果。

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