Alatakis Steven, Stuckey Stephen, Siu Kevin, McLean Catriona
Department of Radiology, Alfred Hospital, Commercial Road, Prahran, Vic. 3181, Australia.
J Clin Neurosci. 2004 Aug;11(6):650-6. doi: 10.1016/j.jocn.2003.08.009.
Gliosarcoma is a rare tumor of the central nervous system, consisting of gliomatous and sarcomatous elements. We present an unusual case of gliosarcoma which demonstrated a variation in phenotype over a six month period, changing from a gliosarcoma with osteosarcomatous differentiation, to a gliosarcoma with no osteosarcomatous component. The initial histological diagnosis was glioblastoma multiforme. Fifteen months later the tumor had transformed into a gliosarcoma demonstrating osteosarcomatous differentiation, with the majority of the tumor consisting of osteoid matrix. Further samples taken six months later revealed gliosarcoma with almost no osteosarcomatous component. It is recognized that glioblastoma can undergo a change in phenotype, transforming into a gliosarcoma. This case demonstrates that ongoing changes in phenotype can occur, especially when the tumor has been treated with chemotherapy and radiotherapy. An understanding of the pathological progression of gliosarcoma will become increasingly important as novel treatments for gliosarcoma and glioblastoma become available.
胶质肉瘤是一种罕见的中枢神经系统肿瘤,由胶质瘤样和肉瘤样成分组成。我们报告了一例不寻常的胶质肉瘤病例,该病例在六个月内表现出表型变化,从具有骨肉瘤分化的胶质肉瘤转变为无骨肉瘤成分的胶质肉瘤。最初的组织学诊断为多形性胶质母细胞瘤。15个月后,肿瘤转变为显示骨肉瘤分化的胶质肉瘤,大部分肿瘤由类骨质基质组成。六个月后采集的进一步样本显示胶质肉瘤几乎没有骨肉瘤成分。人们认识到胶质母细胞瘤可发生表型改变,转变为胶质肉瘤。该病例表明表型会持续发生变化,尤其是在肿瘤接受化疗和放疗后。随着胶质肉瘤和胶质母细胞瘤的新型治疗方法问世,了解胶质肉瘤的病理进展将变得越来越重要。