Department of Neurosurgery, Clinical Neurosciences Center, University of Utah, Salt Lake City, Utah, USA.
Division of Otolaryngology - Head and Neck Surgery, University of Utah, Salt Lake City, Utah, USA.
World Neurosurg. 2020 Sep;141:252. doi: 10.1016/j.wneu.2020.05.059. Epub 2020 May 19.
Sphenoorbital meningiomas require extensive bone removal around the superior and lateral orbital walls, superior orbital fissure, and anterior middle fossa floor. Incomplete resection can lead to recurrence or growth into the cavernous sinus (CS). A 46-year-old woman with a history of childhood leukemia treated with chemotherapy and whole-body radiotherapy had presented to an outside institution in 2004 with headache and vision changes and undergone subtotal resection for right sphenoorbital meningioma. Residual tumor growth caused progressive optic neuropathy, and she underwent multiple orbital decompressions and fractionated radiotherapy. In 2017, she underwent another craniotomy for repeat resection. Additional tumor growth causing neuropathic facial pain syndrome and progressive ophthalmoplegia was treated with orbital enucleation. On referral to our institution, magnetic resonance imaging demonstrated right sphenoorbital and CS meningioma extending into the sella and nearly to the medial border of the contralateral CS. Given her complete ophthalmoplegia and recent orbital enucleation, she underwent revision right frontotemporal craniotomy for radical resection of invasive meningioma, including right internal carotid artery occlusion and CS resection (Video 1). The skull-base defect was repaired with autologous fascia and a free muscle flap. Postoperative transient aphasia and left hemiparesis resolved over several days. At the 1-month follow-up examination, she was neurologically intact, with moderate improvement of facial pain syndrome (preoperative pain score, 9 of 10; postoperative pain score, 6 of 10). Magnetic resonance imaging demonstrated gross total resection. Pathological tissue analysis was consistent with grade 1 meningioma with an increased MIB-1 proliferative index, although, clinically, the tumor behaved more malignantly. The patient provided consent.
蝶眶脑膜瘤需要在眶上壁和外侧壁、眶上裂和中颅窝底周围广泛切除骨。不完全切除可导致复发或生长到海绵窦 (CS)。一名 46 岁女性,儿童期患有白血病,接受化疗和全身放疗,2004 年因头痛和视力改变就诊于外院,行右侧蝶眶脑膜瘤次全切除术。残留肿瘤生长导致进行性视神经病变,她接受了多次眼眶减压和分次放疗。2017 年,她再次行开颅手术行重复切除术。由于额外的肿瘤生长导致神经病理性面部疼痛综合征和进行性眼肌麻痹,她接受了眼眶切除术。转诊至我院时,磁共振成像显示右侧蝶眶和 CS 脑膜瘤延伸至鞍内并几乎延伸至对侧 CS 的内侧缘。鉴于她完全性动眼神经麻痹和最近的眼眶切除术,她接受了右侧额颞部开颅术进行侵袭性脑膜瘤的根治性切除术,包括右侧颈内动脉闭塞和 CS 切除术(视频 1)。颅底缺损用自体筋膜和游离肌肉瓣修复。术后一过性失语和左侧偏瘫在数天内缓解。在 1 个月的随访检查时,她神经功能完整,面部疼痛综合征中度改善(术前疼痛评分为 10 分中的 9 分;术后疼痛评分为 10 分中的 6 分)。磁共振成像显示大体全切除。病理组织分析与 1 级脑膜瘤一致,有较高的 MIB-1 增殖指数,尽管从临床来看,肿瘤的行为更为恶性。患者已同意。