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首页> 外文期刊>Acta Neurochirurgica >Clinical management of petroclival meningiomas and the eternal quest for preservation of quality of life : Personal experiences over a period of 20 years.
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Clinical management of petroclival meningiomas and the eternal quest for preservation of quality of life : Personal experiences over a period of 20 years.

机译:石油斜坡性脑膜瘤的临床管理和对维持生活质量的永恒追求:20年的个人经验。

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BACKGROUND: Within the realm of neurosurgery, petroclival meningiomas are regarded as probably the most difficult tumour to be treated by microsurgery. This is due to the not infrequently large size of the tumours which, although predominantly located in the posterior fossa, may occupy more than one cranial compartment, with often significant space-occupying effect and brain stem compression. Frequent tight brain stem adherence as well as encasement of the basilar artery, its perforators and cranial nerves adds to the sometimes extreme difficulties of surgical tumour removal. Counselling patients as well as pre- and intraoperative decision making in petroclival meningiomas is even more difficult because upon clinical and radiological tumour detection, despite sometimes surprisingly large tumours, clinical symptoms are often only mild. Summarising the complicated development of petroclival meningioma surgery over the last 60 years, this paper represents the conceptual thinking of the author in regard to the treatment of petroclival meningiomas which has evolved over more than two decades, based on a special interest in these treacherous tumours, and accumulated experiences in the treatment of over 150 patients. Surgical concepts and the operative decision-making process are demonstrated in four illustrative cases. METHODS: Over a period of slightly over 20 years, between January 1988 and December 2008, 161 patients with petroclival meningiomas were managed clinically by the author or under his direct surveillance in four academic neurosurgical institutions. The observation period ranged from 4 to 242 months. Thirteen patients were lost to follow-up so, all together, complete data were available for 148 patients. In 119 patients (80%), the tumour was large. Giant tumours accounted for 7% and 11 patients, medium-sized tumours were found in 12 patients (8%) and small tumours in only six patients (4%). Sixty-two percent of the patients had invasion of Meckel's cave or some part of the cavernous sinus, mainly the posterior region to different degrees. All giant tumours and one third of the large tumours extended into more than one cranial fossa. RESULTS: The treatment modalities in the 148 patients were as follows: microsurgery alone was performed in 71 patients (48%), microsurgery and adjuvant radiosurgery in 22 patients (15%) so in 93 patients (63%), altogether, microsurgery was the primary treatment. Twenty-nine patients (20%) underwent radiosurgery as their only treatment, and two patients (1%), during the very early phase of the study period, received radiotherapy. Twenty-four patients (16%) were only observed without any additional therapy. Gross total resection was achieved in 34 patients (37%), and subtotal resection, defined as removal of more than 90% of the tumour volume, was performed in another 36 patients (39%). Radical tumour removal was possible in 76% of the patients. There was no procedure-related death within 3 months post-surgery; the early post-op surgical complication rate was 31% with new neurological deficits or worsening of pre-existing deficits. During the observation period, almost all patients recovered significantly bringing the percentage of permanent neurological deficits, again mainly cranial nerve deficits, down to 22%. CONCLUSIONS: Based on the experiences of the author, the following treatment principles in petroclival meningiomas are proposed: small tumours in asymptomatic patients should be observed. If tumour growth is detected on serial magnetic resonance imaging or treatment is desired by the patient, surgery should be the first choice. Radiosurgery in growing small tumours should be reserved to patients with advanced age or significant co-morbidities. In medium-sized tumours and symptomatic patients, radical surgery should be attempted, if possible by judicious intraoperative judgement. In large and giant petroclival meningiomas, tumour resection as radical as possible judged intraoperatively
机译:背景:在神经外科领域,石油斜坡脑膜瘤被认为是显微外科手术最难治疗的肿瘤。这是由于肿瘤的大小并不罕见,尽管肿瘤主要位于后颅窝,但可能占据一个以上的颅腔,具有明显的占位作用和脑干受压。频繁的紧密脑干附着以及基底动脉,其穿支孔和颅神经的包裹增加了手术切除肿瘤有时的极端困难。在石斜坡脑膜瘤中对患者进行咨询以及术前和术中决策更加困难,因为尽管有令人惊讶的巨大肿瘤,但在临床和放射肿瘤检测中,临床症状通常只是轻度的。总结了过去60年来的岩斜脑膜瘤手术的复杂发展情况,本文基于作者对这些畸形肿瘤的特殊兴趣,代表了作者在治疗岩斜脑膜瘤方面已经超过二十年的概念性思考,积累了超过150名患者的治疗经验。在四个示例性案例中演示了手术概念和手术决策过程。方法:在1988年1月至2008年12月的20多年中,作者或在4家学术神经外科机构的直接监督下对161例石峰脑膜瘤患者进行了临床治疗。观察期为4到242个月。 13名患者失去了随访,因此,总共有148名患者的完整数据。在119例患者(占80%)中,肿瘤较大。巨肿瘤占7%,11例患者,中型肿瘤占12例(8%),小肿瘤仅占6例(4%)。 62%的患者出现了Meckel's洞穴或海绵窦的某些部分,主要是后部区域不同程度的浸润。所有巨大的肿瘤和三分之一的大肿瘤延伸到一个以上的颅窝。结果:148例患者的治疗方式如下:单纯显微外科手术71例(48%),显微外科手术和辅助放射外科手术22例(15%),因此93例(63%)全是显微外科手术。初级治疗。在研究的早期阶段,有29名患者(20%)接受了放射外科手术作为唯一的治疗方法,而两名患者(1%)接受了放射治疗。仅观察到二十四名患者(16%),未进行任何其他治疗。 34例患者(37%)实现了总全切除,另外36例患者(39%)进行了次全切除术,即切除了90%以上的肿瘤。 76%的患者可以根治性切除肿瘤。术后三个月内没有手术相关的死亡;术后早期的手术并发症发生率为31%,伴有新的神经功能缺损或先前存在的缺损加重。在观察期间,几乎所有患者均明显康复,使永久性神经功能缺损(再次主要是颅神经缺损)的百分比降至22%。结论:根据作者的经验,提出了以下治疗岩斜脑膜瘤的原则:应观察无症状患者的小肿瘤。如果通过连续磁共振成像检测到肿瘤生长或患者需要治疗,则应首选手术。成长中的小肿瘤中的放射外科手术应留给年龄较大或合并症的患者使用。对于中型肿瘤和有症状的患者,如果可能,应通过术中明智的判断,尝试进行根治性手术。在巨大和巨大的岩斜脑膜瘤中,术中应尽可能确定肿瘤的根治性切除

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