Shrivastava Raj K, Sen Chandranath, Costantino Peter D, Della Rocca Robert
Department of Neurosurgery, The Center for Cranial Base Surgery, St. Luke's-Roosevelt Medical Center, New York, New York 10019, USA.
J Neurosurg. 2005 Sep;103(3):491-7. doi: 10.3171/jns.2005.103.3.0491.
Sphenoorbital meningiomas (SOMs) are complex tumors involving the sphenoid wing, orbit, and cavernous sinus, which makes their complete resection difficult or impossible. Sphenoidal hyperostosis that results in incomplete resection makes these tumors prone to high rates of recurrence with postoperative morbidity resulting in a nonfunctional globe. High-dose radiation therapy has often been described as the only treatment capable of achieving tumor control, although often at the expense of the patient's progressive visual deterioration.
This series consisted of 25 patients who were retrospectively analyzed over a 12-year period. Visual function was evaluated pre- and postoperatively in all patients. A standardized surgical approach to a frontotemporal craniotomy and orbitozygomatic osteotomy with intra- and extradural drilling of the optic canal and all the hyperostotic bone was performed. Orbital and cranial reconstruction was performed in all patients. The follow-up period was 6 months to 12 years (average 5 years). The patients presented with the classic triad of SOM: proptosis (86%), visual impairment (78%), and ocular paresis (20%). A gross-total resection was achieved in 70% of patients with surgery limited by the superior orbital fissure and the cavernous sinus. Proptosis improved in 96% of patients with 87% improvement in visual function. Ocular paresis improved in 68%, although 20% of patients experienced a temporary ocular paresis postoperatively. There were no perioperative deaths or morbidity related to the surgical approach or reconstruction. Ninety-five percent of patients reported an improved functional orbit. There was tumor recurrence in 8% of patients; in one case recurrence was delayed for longer than 11 years.
Sphenoorbital meningiomas are a distinct category of tumors complicated by potentially extensive hyperostosis of the skull base. Successful resection requires extensive intra- and extradural surgery, necessitating drilling of the optic canal and an orbital osteotomy within anatomical limitations. The bone resection requires reconstruction with autograft, allografts, or alloplast for improved orbital function. All aspects of the clinical triad improved. A radical resection can be achieved with low morbidity, providing a significantly improved clinical outcome in the long-term period.
蝶眶脑膜瘤(SOMs)是累及蝶骨翼、眼眶和海绵窦的复杂肿瘤,这使得其完全切除困难或无法实现。导致切除不完全的蝶骨骨质增生使这些肿瘤易于复发,术后发病率导致眼球功能丧失。高剂量放射治疗常被描述为唯一能够实现肿瘤控制的治疗方法,尽管这往往是以患者视力逐渐恶化为代价。
本系列包括25例患者,对其进行了为期12年的回顾性分析。对所有患者术前和术后的视觉功能进行评估。采用标准化手术方法,进行额颞开颅和眶颧截骨术,同时在硬膜内和硬膜外对视神经管和所有骨质增生的骨进行钻孔。所有患者均进行了眼眶和颅骨重建。随访期为6个月至12年(平均5年)。患者表现出SOM的典型三联征:眼球突出(86%)、视力障碍(78%)和眼肌麻痹(20%)。70%的患者实现了全切除,手术受眶上裂和海绵窦限制。96%的患者眼球突出得到改善,87%患者的视觉功能得到改善。68%的患者眼肌麻痹得到改善,尽管20%的患者术后出现暂时性眼肌麻痹。没有围手术期死亡或与手术方法或重建相关的并发症。95%的患者报告眼眶功能得到改善。8%的患者出现肿瘤复发;其中1例复发延迟超过11年。
蝶眶脑膜瘤是一类独特的肿瘤,伴有潜在广泛的颅底骨质增生。成功切除需要广泛的硬膜内和硬膜外手术,需要在解剖学限制范围内对视神经管进行钻孔和眶截骨术。骨切除需要用自体骨、异体骨或人工骨进行重建,以改善眼眶功能。临床三联征的各个方面均得到改善。可以实现根治性切除,且发病率低,长期来看临床结果显著改善。