Inoue Tomoo, Kanamori Masayuki, Sonoda Yukihiko, Watanabe Mika, Sasajima Toshio, Kamisato Nobuo, Kumabe Toshihiro, Tominaga Teiji
Department of Neurosurgery, Tohoku University Graduate-School of Medicine, Aoba-ku, Sendai-shi, Miyagi, Japan.
No Shinkei Geka. 2008 Aug;36(8):709-15.
Gliomatosis cerebri is a diffuse growth pattern of glioma consisting of exceptionally extensive infiltration of at least three cerebral lobes. We report a case of histologically confirmed glioblastoma multiforme in the cerebellar vermis which occurred 9 years after treatment for gliomatosis cerebri. A 33-year-old woman presented to our department for evaluation of visual disturbance. T2-weighted magnetic resonance (MR) imaging revealed hyperintense lesions in the bilateral frontal and parietal lobes. Histological examination of biopsy specimens from the left frontal lobe lesion demonstrated diffuse infiltration of glial neoplastic cells with preservation of the underlying cytoarchitecture, leading to the diagnosis of gliomatosis cerebri. She received 60 Gy hyperfractionated irradiation to the whole brain, and the lesion responded partially. The patient remained stable for 4 years, but T2-weighted MR imaging 5 years after the initial treatment showed enlargement of the hyperintense area. She received nimustine hydrochloride chemotherapy, and again partial response was observed. However. T1-weighted MR imaging after administration of gadolinium-diethylenetriaminepenta-acetic acid detected enhanced lesions in the cerebellar vermis, cerebellar hemisphere, and left posterior limb of the internal capsule 9 years after the initial treatment, although no abnormal findings were observed on initial and follow-up MR imaging. She underwent subtotal removal of the lesion in the cerebellar vermis. The surgical specimens were characterized by dense proliferation of atypical tumor cells with scattered mitosis and endothelial proliferation. The histological diagnosis was glioblastoma multiforme. The patient received gamma knife irradiation for the remnant lesion in the cerebellar vermis, and the lesions in the cerebellar hemisphere and left posterior limb of the internal capsule, and chemotherapy with temozolomide. However, multiple enhanced lesions were detected in the cerebellar vermis 2 months after the start of the temozolomide chemotherapy, and she died 8 months later. This case suggests that glioblastoma multiforme could develop in the long term after initial treatment for gliomatosis cerebri, and in a location separate from the initial lesion.
大脑胶质瘤病是一种胶质瘤的弥漫性生长模式,其特征是至少三个脑叶出现异常广泛的浸润。我们报告一例经组织学证实的小脑蚓部多形性胶质母细胞瘤病例,该病例发生在大脑胶质瘤病治疗9年后。一名33岁女性因视力障碍前来我院就诊。T2加权磁共振成像显示双侧额叶和顶叶有高信号病变。对左侧额叶病变活检标本进行组织学检查,发现胶质肿瘤细胞弥漫浸润,其下细胞结构保留,诊断为大脑胶质瘤病。她接受了全脑60 Gy超分割照射,病变部分缓解。患者病情稳定4年,但初始治疗5年后的T2加权磁共振成像显示高信号区扩大。她接受了盐酸尼莫司汀化疗,再次观察到部分缓解。然而,在初始治疗9年后,静脉注射钆喷酸葡胺后的T1加权磁共振成像检测到小脑蚓部、小脑半球和内囊左后肢有强化病变,尽管初始和随访磁共振成像均未发现异常。她接受了小脑蚓部病变的次全切除。手术标本的特征是不典型肿瘤细胞密集增殖,有散在的有丝分裂和内皮细胞增殖。组织学诊断为多形性胶质母细胞瘤。患者接受了伽玛刀照射治疗小脑蚓部的残留病变、小脑半球和内囊左后肢的病变,并接受了替莫唑胺化疗。然而,在替莫唑胺化疗开始2个月后,小脑蚓部检测到多个强化病变,她在8个月后死亡。该病例提示,多形性胶质母细胞瘤可在大脑胶质瘤病初始治疗后的长期内发生,且发生部位与初始病变不同。