Department of Neurosurgery, St Mary's Hospital, Fukuoka, Japan.
Department of Pathology, St Mary's Hospital, Fukuoka, Japan.
Neuropathology. 2022 Aug;42(4):282-288. doi: 10.1111/neup.12803. Epub 2022 May 29.
Gliosarcoma is characterized by the presence of alternating lesions of glial and mesenchymal components. Although many mesenchymal components have been reported, there are few reports on glial components. We here report two cases of gliosarcoma. Case 1 was a 42-year-old woman with right hemiparesis and motor aphasia. Magnetic resonance imaging (MRI) identified a tumor in the left frontal lobe. Pathological analysis of the tumor removal specimen revealed gliosarcoma, with a glial component resembling pleomorphic xanthoastrocytoma. Postoperatively, radiotherapy and chemotherapy were conducted, and the patient was symptom-free over 12 months after surgery. Case 2 was a 67-year-old woman with a consciousness disorder and left hemiparesis. MRI revealed a tumor in the right frontal lobe. Pathological analysis of the first tumor removal specimen identified gliosarcoma, with a glial component characterized by large tumor cells. Additionally, the Ki-67 labeling index of the glial component was greater than that of the mesenchymal component, and molecular genetic analysis disclosed a mutation in the telomerase reverse transcriptase (TERT) gene (TERT). Chemotherapy and radiotherapy were performed. Four months later, MRI revealed recurrence, and the second surgery was performed. Pathological analysis revealed giant cell glioblastoma without TERT mutation. The patient died due to tumor progression 12 months after the first surgery. It is essential to continue histopathological evaluation of glial components, and further genetic evaluation on gliosarcoma is required.
胶质肉瘤的特征是存在胶质和间充质成分的交替病变。虽然已经报道了许多间充质成分,但胶质成分的报道很少。我们在此报告两例胶质肉瘤。病例 1 为 42 岁女性,表现为右侧偏瘫和运动性失语。磁共振成像(MRI)发现左额叶肿瘤。肿瘤切除标本的病理分析显示为胶质肉瘤,其中胶质成分类似于多形性黄色星形细胞瘤。术后进行了放疗和化疗,患者术后 12 个月无任何症状。病例 2 为 67 岁女性,表现为意识障碍和左侧偏瘫。MRI 显示右额叶肿瘤。第一次肿瘤切除标本的病理分析确定为胶质肉瘤,其中胶质成分的特点是大肿瘤细胞。此外,胶质成分的 Ki-67 标记指数大于间充质成分,分子遗传学分析显示端粒酶逆转录酶(TERT)基因(TERT)发生突变。进行了化疗和放疗。四个月后,MRI 显示复发,并进行了第二次手术。病理分析显示无 TERT 突变的巨细胞胶质母细胞瘤。患者在第一次手术后 12 个月因肿瘤进展而死亡。继续对胶质成分进行组织病理学评估非常重要,需要对胶质肉瘤进行进一步的遗传评估。