原发性颅骨肿瘤的鉴别诊断 - 单纯骨内硬膜外脑膜瘤的特征。病例报告和文献综述

IF 0.4 Q4 CLINICAL NEUROLOGY
Franz Jooji Onishi , Ana Camila Gandolfi , Rafi Felicio B. Dauar
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引用次数: 0

摘要

本病例报告旨在描述一例罕见的纯骨内脑膜瘤,表现为颅内淋巴结骨病变。本病例报告的患者为一名 67 岁女性,因持续性头痛就诊,接受了 CT 扫描和 MRI 等影像学诊断。讨论放射学检查显示左侧顶骨有浸润性和溶解性异质性病变。全身 PET-CT 扫描显示没有原发受累的迹象。患者成功接受了手术,组织病理学检查确诊为 I 级脑膜上皮性脑膜瘤伴邻近骨质增生。原发性骨内脑膜瘤极为罕见,由于与其他良性和恶性颅骨病变相似,因此诊断难度很大。建议进行边缘较宽的手术切除,组织病理学检查和免疫组化有助于确诊。由于有复发和恶变的可能,因此有必要进行长期监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential diagnosis of a primary skull bone tumor – Characteristics of an purely intraosseous extradural meningioma. Case report and literature review

Objective

This case report aims to describe a rare occurrence of a purely intraosseous meningioma, presenting as a lytic bone lesion in the skull.

Case Report

We present the case of a 67-year-old female patient who presented with a persistent headache and underwent diagnostic imaging, including CT scan and MRI. Surgical resection with wide margins and cranial reconstruction was performed, followed by histopathological examination of the tumor.

Discussion

The radiological investigation revealed an infiltrative and lytic heterogeneous lesion in the left parietal bone. Whole-body PET-CT scan showed no signs of primary involvement. The patient underwent successful surgery, and the histopathological examination confirmed the diagnosis of a grade I meningothelial meningioma with adjacent hyperostosis. Primary intraosseous meningiomas are exceedingly rare and challenging to diagnose due to their mimicry of other benign and malignant skull lesions. Surgical resection with wide margins is recommended, and histopathological examination with immunohistochemistry aids in confirming the diagnosis. Long-term surveillance is necessary due to the potential for recurrence and malignant transformation.

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来源期刊
CiteScore
1.00
自引率
0.00%
发文量
236
审稿时长
15 weeks
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