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首页> 外文期刊>Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery >Management of pediatric intracranial meningiomas: An analysis of 31 cases and review of literature
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Management of pediatric intracranial meningiomas: An analysis of 31 cases and review of literature

机译:小儿颅内脑膜瘤的处理:31例分析及文献复习

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Objective: The purpose of this study is to understand the epidemiology, clinical features, behavior, and the prognostic factors that influence the outcome of intracranial meningiomas in children. Methods: Thirty-one patients with age less than 18 years who underwent surgery for intracranial meningiomas during the period of at 1988-2012 at Voluntary Health Services Hospital, Chennai, India were studied. These formed 3.7 % of the total 831 cases of intracranial meningiomas operated at the institute. Results: The study group included 22 (71 %) males and 9 (29 %) females. The mean age of presentation was 15 years, with the youngest being 9 months old. Two (6 %) had evidence of neurofibromatosis type 2 (NF2). The most common symptoms at presentation were seizures in 11 (35.5 %), weakness of limbs in 11 (35.5 %), and raised intracranial pressure in 10 (32 %). Convexity meningiomas were seen in 16 (51 %) and skull base in 15(49 %). Multiple meningiomas was seen in two (6 %) of the patients and intraventricular location was found in one patient (3 %). Two (6 %) had evidence of NF2. Gross total excision was achieved in 26 (83 %) and subtotal excision in 5 (17 %). WHO grade I was found in 20 (64 %) and higher grade was seen in 11 (36 %). The mean follow-up was 46.2 months. Recurrence was seen in 20 patients (64 %). In patients with higher grade or with recurrence resurgery and radiotherapy was given. Three (9 %) had multiple recurrences. On a mean follow-up of 46.2 months, 25 patients (81 %) were neurologically intact, 5 (16 %) were having moderated disability, and 1 (3 %) patient died. Conclusions: Childhood meningiomas are uncommon lesions with a slight male predominance. They can have a varied clinical presentation. Higher grade is found more frequently compared with adults. Gross total resection is the goal and in higher grade meningiomas radiotherapy helps as a good adjuvant. Though the rate of recurrence is high, resurgery and radiotherapy gives a good outcome.
机译:目的:本研究旨在了解影响儿童颅内脑膜瘤预后的流行病学,临床特征,行为和预后因素。方法:研究对象是1988年至2012年在印度钦奈的自愿健康服务医院接受颅内脑膜瘤手术的年龄在18岁以下的31例患者。这些占该研究所手术的全部831例颅内脑膜瘤病例的3.7%。结果:研究组包括22名男性(71%)和9名女性(29%)。报告的平均年龄为15岁,最小的为9个月大。有2名(6%)有2型神经纤维瘤病(NF2)的证据。呈现的最常见症状是癫痫发作11例(35.5%),四肢无力11例(35.5%)和颅内压升高10例(32%)。凸脑膜瘤见16例(51%),颅底见15例(49%)。在两名(6%)患者中发现了多发脑膜瘤,在一名患者(3%)中发现了脑室内位置。有两个(6%)有NF2证据。总切除量为26(83%),小计切除量为5(17%)。世卫组织I级评分为20(64%),高等级评分为11(36%)。平均随访时间为46.2个月。 20例患者(64%)可见复发。对于等级较高或复发的患者,应进行手术和放疗。 3例(9%)有多次复发。平均随访46.2个月,有25位患者(81%)神经系统完好,5位(16%)中度残疾,1位(3%)死亡。结论:儿童脑膜瘤是一种罕见的病变,男性占主导地位。他们可以有各种各样的临床表现。与成年人相比,高年级学生的学习频率更高。大体全切除是目标,在高级别脑膜瘤放疗中可作为良好的辅助治疗。尽管复发率很高,但手术和放疗可取得良好的效果。

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