Pediatric Meningiomas- A Case Report and Review of the Literature

A. Kelly, T. Tau, Tshilidzi Sidiki
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Abstract

Background: Pediatric meningiomas are relatively rare accounting for only 3% of intracranial neoplasms. As such most of the literature on pediatric meningiomas exists in the form of isolated case reports or as a case series with small patient numbers. Despite this scarcity of literature several important features distinguish pediatric meningiomas from those that occur in adults. These include unique risk factors; a male predominance; larger tumor sizes at presentation; unusual sites of occurrence including intraventricular and parenchymal; higher World Health Organization histological grades; more aggressive clinical behavior and an increased tendency for recurrence. We present a 12-year-old male patient whom presented to our unit with a left fronto-parietal convexity meningioma of an alarming size. Methods: A 12-year-old male patient presented to our unit with an eight-month history of a progressive headache complicated by a two-week history of vomiting. He also complained of progressive weakness of the right side of his body which had worsened to a point that he was no longer independently ambulant. General examination revealed craniomegaly with tortuous scalp veins. Neurological examination revealed a right upper motor neuron facial nerve palsy and a right hemiplegia of 2/5. Radiological investigation revealed an extremely large left fronto-parietal dural based space-occupying lesion which crossed the midline. Due to the adolescent’s progressive neurology he was taken to the operating room for emergency resection of the lesion. Gross total resection was achieved, and histopathological analysis confirmed the lesion to be a fibroblastic meningioma. Result: Post-operatively the patient demonstrated a complete resolution of his hemiplegia and at three weeks post operatively he was already independently ambulant with power 4/5 on the previously hemiplegic side. Conclusion: Despite the notorious features that characterize pediatric meningiomas, as well as an often-intimidating radiological appearance, adherence to standard Neurosurgical operating principles has the best chance of ensuring a successful outcome.
小儿脑膜瘤1例报告及文献复习
背景:小儿脑膜瘤相对罕见,仅占颅内肿瘤的3%。因此,大多数关于儿童脑膜瘤的文献以孤立病例报告或病例系列的形式存在,患者数量很少。尽管缺乏文献,但有几个重要的特征将儿童脑膜瘤与发生在成人中的脑膜瘤区分开来。这些因素包括独特的风险因素;男性优势;出现时肿瘤体积较大;异常发生部位包括脑室内和实质;较高的世界卫生组织组织学等级;更具侵略性的临床行为和增加的复发倾向。我们提出一个12岁的男性患者谁提出了我们的单位左额顶凸出脑膜瘤惊人的大小。方法:一名12岁的男性患者以8个月的进行性头痛合并两周的呕吐史来到我们的科室。他还抱怨他的右侧身体逐渐虚弱,已经恶化到不能独立行动的地步。全身检查显示颅骨大,伴有头皮静脉曲张。神经学检查显示右上运动神经元面神经麻痹,右半瘫2/5。影像学检查显示一个非常大的左侧额顶硬脑膜占位性病变,横跨中线。由于青少年神经系统的进展,他被带到手术室紧急切除病变。大体全切除,组织病理学分析证实病变为纤维母细胞脑膜瘤。结果:术后患者的偏瘫症状完全缓解,术后三周,患者在先前偏瘫的一侧已能独立行走,力量为4/5。结论:尽管小儿脑膜瘤具有臭名昭著的特征,以及通常令人生畏的放射学表现,但坚持标准的神经外科手术原则是确保成功结果的最佳机会。
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