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颅内孤立性外生型脑膜多形性黄色星形细胞瘤:极其罕见病例。

Solitary Extra-axial Intracranial Primary Meningeal Pleomorphic Xanthoastrocytoma: An Extremely Rare Case.

机构信息

Department of Neurosurgery, All India Institute of Medical Sciences, New Delhi, India.

Department of Neurosurgery, All India Institute of Medical Sciences, New Delhi, India.

出版信息

World Neurosurg. 2019 Oct;130:386-390. doi: 10.1016/j.wneu.2019.06.218. Epub 2019 Jul 8.

Abstract

BACKGROUND

Pleomorphic xanthoastrocytomas (PXAs) are a rare type of astrocytoma, which, similar to other gliomas, can rarely arise from glial nests in the meninges, manifesting as an extra-axial mass. We describe a solitary extra-axial intracranial primary meningeal PXA in the pediatric age group, which was masquerading as a tentorial meningioma.

CASE DESCRIPTION

A 9-year-old girl presented with features of raised intracranial pressure. Imaging revealed a dural-based mass in the tentorial region suggestive of a meningioma. This suspicion was further strengthened by intraoperative visualization of an extra-axial tumor with wide tentorial attachment. Near-total excision was achieved. Histopathologic examination established the diagnosis of PXA. Given the tumor's apparent meningeal origin and lack of connection with brain parenchyma in imaging and intraoperative findings, primary meningeal PXA was diagnosed. The absence of coexisting tumor foci on spinal magnetic resonance imaging further refined the diagnosis as solitary extra-axial intracranial primary meningeal PXA. The patient received radiotherapy for the residual tumor and was doing well at 6 months after presentation; however, she was lost to follow-up after that.

CONCLUSIONS

Solitary extra-axial intracranial primary meningeal PXA is an extremely rare entity with only 3 reported cases in the literature including the present case. This is the first report of such a tumor in a pediatric patient. This report also highlights that primary meningeal PXA can manifest as an extra-axial mass lesion and may warrant inclusion in the differential diagnosis of extra-axial mass lesions.

摘要

背景

多形性黄色星形细胞瘤(PXA)是一种罕见的星形细胞瘤,与其他神经胶质瘤一样,也可罕见起源于脑膜中的神经胶质巢,表现为脑外轴内肿块。我们描述了一例儿童期孤立性脑外颅内原发性脑膜 PXA,其表现为天幕脑膜瘤。

病例描述

一名 9 岁女孩出现颅内压升高的特征。影像学显示天幕区硬膜基肿块,提示脑膜瘤。术中观察到与天幕广泛附着的脑外肿瘤进一步加强了这一怀疑。实现了近全切除。组织病理学检查确立了 PXA 的诊断。鉴于肿瘤明显的脑膜起源以及影像学和术中发现与脑实质缺乏联系,诊断为原发性脑膜 PXA。脊髓磁共振成像未见共存肿瘤灶进一步明确诊断为孤立性脑外颅内原发性脑膜 PXA。患者因残余肿瘤接受了放疗,在出现后 6 个月时情况良好,但此后失去了随访。

结论

孤立性脑外颅内原发性脑膜 PXA 是一种极其罕见的实体,文献中仅报告了 3 例,包括本病例。这是首例发生于儿童患者的此类肿瘤报告。本报告还强调,原发性脑膜 PXA 可表现为脑外肿块病变,可能需要纳入脑外肿块病变的鉴别诊断。

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