Ben Nsir A, Ben Hamouda K, Hammedi F, Kilani M, Hattab N
Department of Neurosurgery, Fattouma Bourguiba University Hospital - University of Medicine of Monastir, Monastir, Tunisia.
Department of Neurosurgery, The Tunisian National Institute of Neurology - University of Medicine of Tunis El Manar, Tunis, Tunisia.
Neurol Neurochir Pol. 2016 Jul-Aug;50(4):297-302. doi: 10.1016/j.pjnns.2016.04.003. Epub 2016 Apr 26.
While bone invasion and hyperostosis are frequent phenomena in meningiomas, primary intraosseous meningiomas are rare and their occurrence in the skull base is an extraordinary exception. Moreover, radiation-induced meningiomas represent a unique clinical dilemma given the fact that patients with these tumors had often received a prior full course of radiotherapy.
A 42-year-old man presented with a 3-month history of progressively worsening facial asymmetry. His medical history was consistent for a posterior cranial fossa irradiation at the age of 6 years for a non-confirmed brain stem tumor. On admission his Karnofsky performance status was graded as 50% and his neurological examination showed a complete right facial nerve paralysis and hearing impairment. Computed tomography and magnetic resonance imaging demonstrated an osteolytic tumor invading the whole right petrous bone without intracranial involvement.
As the tumor reached the external auditory canal, a tissue sample was obtained locally. Pathological examination of the lesion identified a grade II clear cell meningioma and the patient was consequently addressed for an intensity modulated radiation therapy. His condition remained unchanged till the most recent follow-up examination, 8 months later.
To the best of our knowledge, a radiation induced osteolytic clear cell meningioma of the petrous bone has not been previously reported. As little literature exists regarding the use of adjuvant therapies for these tumors, intensity modulated radiation therapy remains an attractive treatment option in case of pervious irradiation and general status alteration.
虽然骨侵犯和骨质增生在脑膜瘤中较为常见,但原发性骨内脑膜瘤罕见,其发生于颅底更是极为特殊的情况。此外,鉴于患有这些肿瘤的患者通常曾接受过完整疗程的放疗,放射性诱导的脑膜瘤代表了一种独特的临床困境。
一名42岁男性,有3个月逐渐加重的面部不对称病史。他的病史显示6岁时因未确诊的脑干肿瘤接受过后颅窝放疗。入院时其卡氏评分(Karnofsky performance status)为50%,神经系统检查显示右侧面神经完全麻痹及听力障碍。计算机断层扫描和磁共振成像显示一个溶骨性肿瘤侵犯了整个右侧岩骨,无颅内受累。
由于肿瘤累及外耳道部位,局部获取了组织样本。病变的病理检查确定为II级透明细胞脑膜瘤,因此患者接受了调强放射治疗。直至8个月后的最近一次随访检查,其病情一直未变。
据我们所知,此前尚未报道过放射性诱导的岩骨溶骨性透明细胞脑膜瘤。由于关于这些肿瘤辅助治疗的文献较少,对于既往接受过放疗且一般状况改变的情况,调强放射治疗仍是一种有吸引力的治疗选择。