伴有惊厥症状的出血性脑膜瘤:罕见的顶壁脑膜瘤

Dinh Thi Phuong Hoai, Duong Ngoc Thanh Van, Phan Quoc Tho, Nguyen Ngoc Anh Thu, Le Trong Phuoc, Le Trong Hieu, Nguyen Vinh Lac, Vo Ba Tuong, N. T. Minh
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引用次数: 0

摘要

脑膜瘤是最常见的轴外非神经胶质颅内肿瘤,发病率为2.3-5.5/10000,占成人所有原发性脑肿瘤诊断的20%-30%。与肿瘤内出血相关的脑膜瘤非常罕见,发生在0.5%-2.4%的个体中。在此,我们报告一个罕见的出血性脑膜瘤伴惊厥症状。该病例是一名68岁的妇女,因严重头痛和抽搐入院。计算机断层扫描显示右顶叶4×3×2.5cm的异质性病变增加。脑磁共振成像(MRI)显示一个大体稳定、均匀增强的轴外肿块,尺寸为43×33×28 mm,小的钙化外周肿瘤内出血。组织病理学显示多细胞脑膜瘤出血区(世界卫生组织I级)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hemorrhagic Meningioma With Symptom of Convulsion: A Rare Presentation of Parietal Meningioma
Meningioma is the most common, extra-axial, non-glial intracranial tumor with an incidence of 2.3- 5.5/100000, accounting for 20%-30% of all primary brain tumor diagnoses in adults. Meningiomas associated with intratumoral hemorrhage are very rare occurring in 0.5%-2.4%. of individuals. Herein, we report a rare case of hemorrhagic meningioma with the symptom of convulsion. The case was a 68-year-old woman admitted to the hospital with severe headache and convulsions. Computed tomography revealed an increase in heterogeneous lesion measuring 4×3×2.5 cm at the right parietal lobe. Brain magnetic resonance imaging (MRI) showed a grossly stable homogeneously enhancing extra-axial mass measuring 43×33×28 mm, small calcified peripheral, intratumoral hemorrhage. Histopathology showed a multi-celled meningioma with bleeding areas (WHO grade I).
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