首页> 外文期刊>Neuropathology: official journal of the Japanese Society of Neuropathology >Lymphoplasmacyte-rich meningioma: A convexity mass with regional enhancement in the adjacent brain parenchyma
【24h】

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

机译:富含淋巴胞质的脑膜瘤:在邻近脑实质中具有局部增强的凸状肿块

获取原文
获取原文并翻译 | 示例
       

摘要

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.
机译:富含淋巴胞质的脑膜瘤(LPM)是一种罕见的良性脑膜瘤变体,其特征是大量的炎性细胞浸润和可变比例的脑膜肿瘤成分。在这里,我们报告了37岁女性右额凸处的LPM的临床病理特征。该患者在怀孕32周时开始出现全身性强直阵挛发作。病变在T1加权MRI上显示低强度,在T2加权图像上显示高强度,周围有实质性水肿。该肿块表现出enhancement增强和硬脑膜尾征。而且,明显的多个线性增强灶扩散穿过龈沟并进入附近的脑实质。分娩后1个月,整块切除肿块,附着的硬脑膜和邻近的脑组织。从组织学上讲,位于硬膜下腔的肿块由B淋巴细胞和T淋巴细胞以及浆细胞的混合物组成。在肿块内,观察到多个小脑膜小细胞,显示对上皮膜抗原和波形蛋白具有免疫反应性。炎性细胞也浸润了蛛网膜下腔和Virchow-Robin腔以及硬脑膜。大脑皮层显示缺血变化,但无肿瘤细胞侵袭。根据这些组织学特征,病变似乎是LPM,脑膜内皮成分不明显,炎症浸润广泛。这种情况似乎提供了有关此变异的发病机理的有用信息。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号