Suppr超能文献

儿童颅内非脑膜附着性异时性脑膜瘤——罕见病例报告及文献复习。

Metachronous intracranial meningiomas without dural attachment in a child - Rare case report and review of literature.

机构信息

Department of Neurosurgery, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, 560029, Karnataka, India.

Department of Neuropathology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, 560029, Karnataka, India.

出版信息

Childs Nerv Syst. 2024 Dec;40(12):4265-4269. doi: 10.1007/s00381-024-06582-7. Epub 2024 Aug 24.

Abstract

INTRODUCTION

Meningiomas in children are rare, constituting less than 5% of all paediatric brain tumours and less than 2% of all meningiomas. Multiple meningiomas (synchronous or metachronous) are even more uncommon, typically occurring due to radiation exposure or in patients with phacomatoses like Neurofibromatosis II. This report presents the case of a child with metachronous meningiomas without dural attachment in unusual locations, along with their management.

PURPOSE

This report aims to describe a rare paediatric case of metachronous meningiomas without dural attachment, detailing their presentation, treatment, and outcomes.

CASE DETAILS

A 2-year-old female presented with headaches, irritability, and excessive crying for one year. A CT scan revealed a mass in the fourth ventricle, causing obstruction, which was surgically decompressed. The biopsy confirmed a clear cell meningioma, WHO grade II. A follow-up MRI identified a new lesion in the suprasellar area six months later, for which she underwent right pterional craniotomy and gross total resection, which turned out to be a clear cell meningioma, WHO grade II. The patient recovered well and remained asymptomatic, with no recurrence on MRI at one-year follow-up.

CONCLUSION

This case highlights the unusual presentation of metachronous clear cell meningiomas without dural attachment in a young child. Surgical excision resulted in a favourable outcome, though long-term follow-up is essential due to the high propensity for recurrence.

摘要

介绍

儿童脑膜瘤较为罕见,占儿童脑肿瘤的比例不到 5%,占所有脑膜瘤的比例不到 2%。多发性脑膜瘤(同时性或异时性)更为罕见,通常由于辐射暴露或神经纤维瘤病 II 等神经皮肤疾病而发生。本报告介绍了一例无硬脑膜附着的异时性脑膜瘤患儿的病例,以及其治疗情况。

目的

本报告旨在描述一例罕见的儿童异时性无硬脑膜附着脑膜瘤病例,详细描述其表现、治疗和结果。

病例详情

一名 2 岁女性因头痛、烦躁和过度哭泣一年就诊。CT 扫描显示第四脑室有一肿块,导致梗阻,行手术减压。活检证实为 II 级透明细胞脑膜瘤。6 个月后,随访 MRI 发现鞍上区出现新病变,行右侧翼点开颅肿瘤全切除,结果为 II 级透明细胞脑膜瘤。患者恢复良好,无症状,1 年随访时 MRI 未见复发。

结论

本例突出了儿童罕见的异时性无硬脑膜附着透明细胞脑膜瘤的表现。手术切除结果良好,但由于复发倾向高,需要长期随访。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验