Kakkar Neha, Kaur Jaspreet, Singh Gunjesh Kumar, Singh Pragya, Siraj Fouzia, Gupta Ajay
Department of Radiotherapy, VMMC & Safdarjung Hospital, New Delhi 110029, India.
Department of Pathology, VMMC & Safdarjung Hospital, New Delhi 110029, India.
World J Oncol. 2017 Apr;8(2):53-57. doi: 10.14740/wjon998w. Epub 2017 May 4.
Gliosarcoma is a rare central nervous system (CNS) malignancy. It is characterized by classical biphasic histological pattern with both glial and sarcomatous components, often seen in fifth and sixth decade of life. They are generally located in the supratentorial region. Due to its rarity, exact treatment recommendations are not available in literature. Since it is considered as a variant of glioblastoma multiforme (GBM), it is treated with surgery followed by adjuvant radiotherapy and temozolomide-based chemotherapy. We present a series of four cases of this rare malignancy that were treated at our institute.
胶质肉瘤是一种罕见的中枢神经系统(CNS)恶性肿瘤。其特征为具有神经胶质和肉瘤成分的典型双相组织学模式,常见于50至60岁。它们通常位于幕上区域。由于其罕见性,文献中尚无确切的治疗建议。由于它被认为是多形性胶质母细胞瘤(GBM)的一种变体,治疗方法是手术,随后进行辅助放疗和基于替莫唑胺的化疗。我们报告了在我们研究所治疗的一系列4例这种罕见恶性肿瘤的病例。