Temporoparietal Gliosarcoma : A Case Report with Literature Review

F. Ahmad, B. Hernowo, A. Adam, M. Arifin
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引用次数: 1

Abstract

Gliosarcoma (GSM) is a primary tumor of the central nervous systemcomposed of both malignant glial and sarcomatous elements. GSM isclassified as grade IV according to World Health Organization (WHO)and regarded as aggressive tumor and often requires both surgeryand radiotherapy. The incidence of GSM is between 1.8%-2.8% ofall malignant gliomas and thus represents an exceptionally rareneoplasm. Consequently, our knowledge about this entity is limited tosmall retrospective case series and case reports. Here, we describe acase of a 46-year-old male with progressive right extremity weakness,accompanied with aphasia. Imaging studies showed a tumor mass inthe left temporoparietal region. Surgery was performed and gross totalremoval was achieved. Histopathology finding established a diagnosisof GSM. The extremity weakness was improved postoperatively withina week.
颞顶叶胶质肉瘤1例并文献复习
神经胶质瘤(GSM)是中枢神经系统的原发性肿瘤,由恶性神经胶质瘤和肉瘤组成。GSM被世界卫生组织(WHO)列为IV级,被认为是侵袭性肿瘤,通常需要手术和放疗。GSM的发病率在所有恶性胶质瘤的1.8%-2.8%之间,因此是一种非常罕见的肿瘤。因此,我们对该实体的了解仅限于小型回顾性病例系列和病例报告。在这里,我们描述了一个46岁的男性进行性右肢无力,并伴有失语的情况。影像学检查显示左侧颞顶区有肿块。手术完成,大体全切除。组织病理学结果确定了GSM的诊断。术后1周内四肢无力得到改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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