{"title":"Metachronous intracranial meningiomas without dural attachment in a child - Rare case report and review of literature.","authors":"Anup Roy, Abhinith Shashidhar, Gyani J S Birua, Shilpa Rao, Karthik Kulanthaivelu, Arivazhagan Arimappamagan","doi":"10.1007/s00381-024-06582-7","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>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.</p><p><strong>Purpose: </strong>This report aims to describe a rare paediatric case of metachronous meningiomas without dural attachment, detailing their presentation, treatment, and outcomes.</p><p><strong>Case details: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":9970,"journal":{"name":"Child's Nervous System","volume":null,"pages":null},"PeriodicalIF":1.3000,"publicationDate":"2024-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Child's Nervous System","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00381-024-06582-7","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
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.
导言:儿童脑膜瘤非常罕见,在所有儿童脑肿瘤中占比不到 5%,在所有脑膜瘤中占比不到 2%。多发性脑膜瘤(同步或非同步)则更为罕见,通常是由于放射线照射或患有神经纤维瘤病 II 等噬瘤体疾病所致。目的:本报告旨在描述一例罕见的无硬脑膜附着的同步脑膜瘤儿科病例,详细介绍其表现、治疗和结果:病例详情:一名两岁的女孩因头痛、易怒和过度哭闹就诊一年。CT 扫描显示第四脑室有肿块,导致阻塞,经手术减压。活检证实为透明细胞脑膜瘤,WHO II 级。六个月后,随访的核磁共振检查发现星状上区有新的病变,为此她接受了右侧翼状开颅手术和全切术,结果发现是透明细胞脑膜瘤,WHO II 级。患者恢复良好,无任何症状,随访一年,核磁共振检查未见复发:本病例突显了幼儿无硬膜附着的透明细胞脑膜瘤的不寻常表现。手术切除的结果很好,但由于复发的可能性很高,因此必须进行长期随访。
期刊介绍:
The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.