Johnson T E, Weatherhead R G, Nasr A M, Siqueira E B
King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
J Pediatr Ophthalmol Strabismus. 1993 Jan-Feb;30(1):43-7. doi: 10.3928/0191-3913-19930101-11.
Meningiomas arising from the optic nerve or secondarily invading the orbit from the intracranial cavity are uncommonly encountered in children. Ectopic (extradural) meningiomas are exceedingly rare orbital tumors that do not originate from either the optic nerve or the intracranial meninges. We evaluated and treated two boys aged 7 and 10 years with probable primary ectopic (extradural) orbital meningiomas. Both patients presented with a gradual onset of progressive, painless proptosis. In addition, computed tomographic scans demonstrated involvement of the superomedial orbit without bony erosion or hyperostosis, but with expansion of the adjacent sinus. Neither tumor demonstrated attachment to the optic nerve or intracranial extension at the time of surgery. Both patients were successfully treated with complete surgical excision. Evaluation did not reveal the presence of neurofibromatosis in either child.
起源于视神经或继发于颅内腔侵犯眼眶的脑膜瘤在儿童中并不常见。异位(硬膜外)脑膜瘤是极其罕见的眼眶肿瘤,既不起源于视神经也不起源于颅内脑膜。我们评估并治疗了两名分别为7岁和10岁的男孩,他们可能患有原发性异位(硬膜外)眼眶脑膜瘤。两名患者均表现为渐进性、无痛性眼球突出逐渐出现。此外,计算机断层扫描显示眶上内侧受累,无骨质侵蚀或骨质增生,但相邻鼻窦有扩张。手术时,两个肿瘤均未显示与视神经相连或颅内延伸。两名患者均通过完整的手术切除成功治疗。评估未发现任何一名儿童患有神经纤维瘤病。