Schaller C, Meyer B, Jung A, Erkwoh A, Schramm J
Neurochirurgische Klinik, Rheinische Friedrich-Wilhelms-Universität Bonn.
Zentralbl Neurochir. 2002;63(2):59-64. doi: 10.1055/s-2002-33971.
Growth patterns of tentorial meningiomas are related to the deep cerebral venous system and to cranial nerves IV-XI. Localization and surgical aggressiveness are decisive for the outcome to be expected.
n = 25 patients (22 f, 3 m), aged from 26-77 (mean: 56.4) years underwent microsurgical removal of their tentorial meningioma. Tumor size was as follows: n = 11 < 3 cm, n = 6 3-5 cm, n = 8 > 5 cm. The median of the preoperative Karnofsky scores was 90. The operative approaches chosen were suboccipital in n = 14, subtemporal in n = 6, occasionally a combined supra- and infratentorial approach was chosen. Data regarding surgery, histology and postoperative course were available through the patient's charts and through outpatient clinic.
n = 20 (80%) of the tumors were rated WHO grade I, n = 5 (20%) WHO grade II. Tumor removal according to Simpson was degrees I in n = 9 (36%), degrees II in n = 14 (56%), degrees III in n = 2 (8%). Mortality was 0%. In n = 6 patients (24%) neurological worsening, mainly due to transient cranial nerve deficits was noted. Surgical complications (CSF fistula, wound healing problems) occurred in n = 5 patients (20%). The median of the postoperative Karnofsky scores on last follow up was 90 after a median of 41.9 months. Two patients (8%), one of whom underwent reoperation developed tumor recurrency during follow up.
Neurological deficits following microsurgical removal of tentorial meningiomas are transient in the majority of patients. The apparently high rate of incomplete tumor resection (app. 60% Simpson grades II and III) is due to the close topographical relationship of these tumors with important neurovascular structures. Thus, the operative strategy should not be excessively aggressive, but rather take into account the option to observe residual tumor or to apply additional stereotactic convergent beam radiation in selected cases.
小脑幕脑膜瘤的生长模式与大脑深部静脉系统及Ⅳ - Ⅺ对脑神经有关。肿瘤的定位和手术侵袭性对预期结果起决定性作用。
25例患者(22例女性,3例男性),年龄26 - 77岁(平均56.4岁),接受了小脑幕脑膜瘤的显微手术切除。肿瘤大小如下:11例<3cm,6例3 - 5cm,8例>5cm。术前卡诺夫斯基评分的中位数为90分。所选择的手术入路为:14例采用枕下入路,6例采用颞下入路,偶尔采用幕上和幕下联合入路。通过患者病历和门诊可获取有关手术、组织学及术后病程的数据。
20例(80%)肿瘤为世界卫生组织(WHO)Ⅰ级,5例(20%)为WHOⅡ级。根据辛普森分级,肿瘤切除程度为Ⅰ级的有9例(36%),Ⅱ级的有14例(56%),Ⅲ级的有2例(8%)。死亡率为0%。6例患者(24%)出现神经功能恶化,主要原因是短暂性脑神经功能缺损。5例患者(20%)发生手术并发症(脑脊液漏、伤口愈合问题)。末次随访时术后卡诺夫斯基评分的中位数为90分,中位随访时间为41.9个月。2例患者(8%)在随访期间出现肿瘤复发,其中1例接受了再次手术。
大多数患者在小脑幕脑膜瘤显微手术后出现的神经功能缺损是短暂性的。肿瘤切除不完全的发生率明显较高(约60%为辛普森Ⅱ级和Ⅲ级),这是由于这些肿瘤与重要神经血管结构的解剖位置关系密切。因此,手术策略不应过于激进,而应考虑在某些情况下观察残留肿瘤或采用额外的立体定向聚束放射治疗。