颅硬脑膜增厚的一种不寻常原因。

IF 0.9 Q4 CLINICAL NEUROLOGY Case Reports in Neurological Medicine Pub Date : 2020-10-29 eCollection Date: 2020-01-01 DOI:10.1155/2020/8877738
Jing Ming Yeo, Donald MacArthur, Jillian Davis, Ian Scott, Bruno Gran
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引用次数: 1

摘要

我们描述了一个不寻常的原因颅硬脑膜增厚在一个老年女性慢性脑膜炎症过程。70岁华裔新加坡女性,每日慢性头痛病史,无其他脑膜体征。连续脑MRI显示左侧额叶区进行性厚脑膜和轻脑膜增强,伴有血管源性水肿,右侧额叶区类似表现,但程度较轻,双侧鼻窦持续炎性改变。调查检查显示ESR长期升高,CRP正常,ANCA阴性,血清IgA kappa副蛋白长期升高。骨髓穿刺活检提示低水平浆细胞病变。嗅裂活检未发现igg4相关疾病或血管炎,未见明显浆细胞浸润。脑膜活检的组织病理学检查显示诊断为斑状脑膜瘤(WHO, 2016;一级)引起不寻常的肉芽肿反应。我们讨论这种罕见形式的脑膜瘤的放射学和组织学关系。临床医生在鉴别诊断硬脑膜线状增厚和增强时可考虑斑块脑膜瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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An Unusual Cause of Cranial Dural Thickening.

We describe an unusual cause of cranial dural thickening in an elderly female with a chronic meningeal inflammatory process. A 70-year-old ethnically Chinese, Singaporean female presented with a history of chronic daily headache with no other meningeal signs. Serial MRI brains showed progressive pachymeningeal and leptomeningeal enhancement in the left frontal region with underlying vasogenic oedema, similar appearances in the right frontal region to a lesser extent, and persistent inflammatory changes in her bilateral paranasal sinuses. Investigative work-up showed a chronically raised ESR with a normal CRP, negative ANCA, and a chronically raised serum IgA kappa paraprotein. Bone marrow trephine biopsy was suggestive of a low level plasma cell disorder. Olfactory cleft biopsy showed no evidence of IgG4-related disease or vasculitis and no significant plasma cell infiltrate. Histopathological examination from a meningeal biopsy revealed a diagnosis of an en-plaque meningioma (the WHO, 2016; Grade I) causing an unusual granulomatous reaction. We discuss the radiological and histological relations of this rare form of meningioma. Clinicians can consider en-plaque meningioma in the differential diagnosis of linear dural thickening and enhancement.

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自引率
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发文量
26
审稿时长
11 weeks
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