Erman Tahsin, Göçer A Iskender, Tuna Metin, Erdoğan Seyda, Zorludemir Suzan
Department of Neurosurgery, Cukurova University School of Medicine, Balcali, Adana, Turkey.
Neurosurg Focus. 2003 Oct 15;15(4):ECP2. doi: 10.3171/foc.2003.15.4.8.
This 65-year-old man presented with a very rare malignant meningioma in the trigonum of the right lateral ventricle. Neurological examination showed bilateral papilledema. Magnetic resonance imaging revealed a solid, enhancing tumor in the right trigonum with a hypointense cystic component located in the center of the tumor. The lesion was totally resected via a superior parietooccipital transcortical approach. Histological examination showed an anaplastic (malignant) meningioma with architectural disarray, high mitotic activity (20/10 hpf), necrosis, and cytological atypism. As in our case, heterogeneous signal, due to necrotic tissue and frequently demonstrated on both T1- and T2-weighted sequences, is suggestive of an aggressive type of meningioma.
这名65岁男性患者患有位于右侧脑室三角区的一种极为罕见的恶性脑膜瘤。神经系统检查显示双侧视乳头水肿。磁共振成像显示右侧三角区有一个实性强化肿瘤,肿瘤中心有一个低信号囊性成分。通过顶枕部经皮质入路将病变完全切除。组织学检查显示为间变性(恶性)脑膜瘤,具有结构紊乱、高有丝分裂活性(每10个高倍视野20个)、坏死和细胞异型性。正如我们的病例一样,由于坏死组织导致的异质性信号在T1加权和T2加权序列上经常显示,提示为侵袭性脑膜瘤。