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富含淋巴浆细胞的脑膜瘤:凸面肿块,邻近脑实质有区域性强化。

Lymphoplasmacyte-rich meningioma: a convexity mass with regional enhancement in the adjacent brain parenchyma.

机构信息

Department of Neurosurgery, Nagaoka Red Cross Hospital, Nagaoka, Japan.

出版信息

Neuropathology. 2012 Apr;32(2):174-9. doi: 10.1111/j.1440-1789.2011.01236.x. Epub 2011 Jul 7.

DOI:10.1111/j.1440-1789.2011.01236.x
PMID:21732989
Abstract

Lymphoplasmacyte-rich meningioma (LPM) is a rare, benign variant of meningioma, characterized by massive inflammatory cell infiltration and a variable proportion of meningothelial tumorous elements. Here we report the clinicopathological features of an LPM located at the right frontal convexity in a 37-year-old woman. The patient had suffered an initial generalized tonic-clonic seizure when she was 32 weeks pregnant. The lesion exhibited low intensity on T1-weighted MRI and high intensity on T2-weighted images, with surrounding parenchymal edema. The mass exhibited gadolinium enhancement with dural tail signs. Moreover, multiple foci of linear enhancement spreading through the sulci and into the nearby brain parenchyma were evident. At 1 month after parturition, en bloc removal of the mass, the attached dura mater and adjacent brain tissue was performed. Histologically, the mass located in the subdural space was composed of a mixture of B- and T-lymphocytes and plasma cells. Within the mass, multiple small lobules of meningothelial cells showing immunoreactivity for epithelial membrane antigen and vimentin were observed. The inflammatory cells had also infiltrated the subarachnoid and Virchow-Robin spaces, and the dura mater. The cerebral cortex showed ischemic changes, but no tumor cell invasion. On the basis of these histological features, the lesion appeared to be LPM with an inconspicuous meningothelial component and extensive inflammatory infiltration. This case appears to provide useful information on the pathogenesis of this variant.

摘要

淋巴浆细胞丰富型脑膜瘤(LPM)是脑膜瘤的一种罕见的良性变体,其特征是大量炎症细胞浸润和脑膜上皮肿瘤成分的可变比例。在这里,我们报告了一位 37 岁女性右额凸面 LPM 的临床病理特征。患者在 32 周妊娠时首次出现全面强直阵挛性发作。病变在 T1 加权 MRI 上呈低信号,在 T2 加权图像上呈高信号,伴有周围实质水肿。肿块呈钆增强,伴有脑膜尾征。此外,还可见多个线性增强灶通过脑沟延伸至附近脑实质。产后 1 个月,行肿块、附着硬脑膜和邻近脑组织的整块切除。组织学上,位于硬膜下腔的肿块由 B 细胞和 T 细胞以及浆细胞混合组成。在肿块内,观察到多个具有上皮膜抗原和波形蛋白免疫反应性的脑膜上皮细胞小小叶。炎症细胞也浸润了蛛网膜下腔和 Virchow-Robin 间隙以及硬脑膜。大脑皮层显示缺血性改变,但无肿瘤细胞侵犯。基于这些组织学特征,病变似乎是 LPM,伴有不明显的脑膜上皮成分和广泛的炎症浸润。该病例似乎为这种变体的发病机制提供了有用的信息。

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Lymphoplasmacyte-rich meningioma: our experience with 19 cases and a systematic literature review.富于淋巴细胞-浆细胞型脑膜瘤:我们19例病例的经验及系统的文献综述
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