Lee Ji-Hye, Kim Jong Hyun, Kwon Taek-Hyun
Department of Neurosurgery, VHS Medical Center, Seoul, Korea.
Department of Neurosurgery, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Korea.
J Korean Neurosurg Soc. 2017 May;60(3):380-384. doi: 10.3340/jkns.2015.0303.006. Epub 2017 May 1.
Glioblastoma multiforme (GBM) is located most frequently in the cerebral hemispheres. Glioblastoma presenting as an extraaxial mass of cerebellopontine angle (CPA) is very rare in adults. We report a rare case of GBM arising in the CPA. The patient was a 71-year-old female, who complained of progressive gait disturbance and poor memory. Initial magnetic resonance imaging (MRI) revealed a 1.4×1.3 cm mass in the left CPA, with broad base to the petrous bone, showing homogenous enhancement. Follow-up MRI showed a rapid increase in size of mass (2.7×2.2 cm) with a necrotic portion. A stereotactic biopsy was done under the guidance of navigation system, and the histopathologic diagnosis was GBM, World Heath Organization grade IV. Further surgical resection was not performed considering her general condition, and the patient underwent concurrent chemotherapy with radiation therapy. Although rare, the possibility of glioblastoma should be included in the differential diagnosis of atypical CPA tumor.
多形性胶质母细胞瘤(GBM)最常发生于大脑半球。在成人中,表现为小脑桥脑角(CPA)轴外肿块的胶质母细胞瘤非常罕见。我们报告一例罕见的起源于CPA的GBM病例。患者为一名71岁女性,主诉进行性步态障碍和记忆力减退。最初的磁共振成像(MRI)显示左侧CPA有一个1.4×1.3 cm的肿块,基底部宽阔,附着于岩骨,呈均匀强化。随访MRI显示肿块大小迅速增加(2.7×2.2 cm),出现坏死部分。在导航系统引导下进行了立体定向活检,组织病理学诊断为GBM,世界卫生组织IV级。考虑到患者的一般状况,未进行进一步的手术切除,患者接受了同步放化疗。尽管罕见,但在非典型CPA肿瘤的鉴别诊断中应考虑胶质母细胞瘤的可能性。