Bikmaz Kerem, Mrak Robert, Al-Mefty Ossama
Department of Neurosurgery, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205-7199, USA.
J Neurosurg. 2007 Nov;107(5):905-12. doi: 10.3171/JNS-07/11/0905.
OBJECT: The hyperostosis frequently associated with sphenoid wing meningiomas is actual invasion of bone by the tumor. The intracranial portion of the tumor is usually thin with en plaque spread, and the tumor tends to invade the orbit through the superior orbital fissure. METHODS: The authors reviewed the records of 67 patients with sphenoid wing meningiomas who underwent surgery at the University of Arkansas for Medical Sciences between 1994 and 2004. In all 67 cases, the surgery was performed by the senior author. Seventeen of the patients had the distinguishing characteristics of hyperostotic sphenoid wing meningiomas-extensive bone invasion, en plaque dural involvement, and a minimal intracranial mass with minimal orbital involvement. In all patients, hyperostosis was determined on the basis of preoperative neuroimaging. Histopathological evaluation of bone specimens was performed in 14 cases. Estrogen and progesterone receptor expression and Ki 67 labeling were evaluated in all specimens. Chromosome analysis was performed in all tumors resected since 2001 (seven cases). Particular attention was paid to removing all involved bone and dura mater. RESULTS: Total removal was achieved in 14 cases (82.3%), with only one recurrence (7.1%) over a mean follow-up period of 36 months (range 5-72 months). Radical resection was followed by cranioorbital reconstruction to prevent enophthalmos and to obtain good cosmetic results. No deaths or serious complications occurred in association with surgery. Proptosis was corrected in all cases and visual acuity improved in seven (70%) of 10 cases. Revision of the orbital reconstruction was required because of postoperative enophthalmos (two cases) or restricted postoperative ocular movement (one case). CONCLUSIONS: Sphenoid wing meningiomas frequently invade bone, although such invasion does not represent malignancy. These lesions are generally histologically benign. Total removal with a prospect for cure and visual preservation should be the goal of treatment. This requires extensive drilling of the invaded bone and extensive excision of the involved dura. When the optic canal is involved, it should be decompressed. Extensive bone resection should be followed by cranioorbital reconstruction for good cosmesis and to prevent enophthalmos.
目的:蝶骨嵴脑膜瘤常伴发的骨质增生实际上是肿瘤对骨的侵犯。肿瘤的颅内部分通常较薄,呈扁平状蔓延,且肿瘤倾向于通过眶上裂侵犯眼眶。 方法:作者回顾了1994年至2004年间在阿肯色大学医学科学部接受手术的67例蝶骨嵴脑膜瘤患者的病历。所有67例手术均由资深作者完成。其中17例患者具有骨质增生型蝶骨嵴脑膜瘤的特征——广泛的骨侵犯、硬脑膜扁平状受累、颅内肿块极小且眼眶受累极少。所有患者均根据术前神经影像学检查确定有骨质增生。对14例患者的骨标本进行了组织病理学评估。对所有标本均评估了雌激素和孕激素受体表达以及Ki 67标记。对2001年以来切除的所有肿瘤(7例)进行了染色体分析。特别注意切除所有受累的骨和硬脑膜。 结果:14例(82.3%)实现了全切,平均随访36个月(范围5 - 72个月)仅1例复发(7.1%)。根治性切除后进行颅眶重建以防止眼球内陷并获得良好的美容效果。手术未发生死亡或严重并发症。所有病例的眼球突出均得到矫正,10例中有7例(70%)视力改善。因术后眼球内陷(2例)或术后眼球运动受限(1例)需要对眶重建进行修正。 结论:蝶骨嵴脑膜瘤常侵犯骨质,尽管这种侵犯并不代表恶性。这些病变在组织学上一般为良性。以治愈和保留视力为前景的全切应是治疗目标。这需要广泛磨除受累骨质并广泛切除受累硬脑膜。当视神经管受累时,应进行减压。广泛的骨切除后应进行颅眶重建以获得良好的美容效果并防止眼球内陷。
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