Fukuda Aya, Queiroz Luciano de Souza, Reis Fabiano
Universidade Estadual de Campinas, Faculdade de Ciências Médicas, Departamento de Radiologia, Campinas SP, Brazil.
Universidade Estadual de Campinas, Faculdade de Ciências Médicas, Departamento de Anatomia Patológica, Campinas SP, Brazil.
Arq Neuropsiquiatr. 2020 Feb;78(2):112-120. doi: 10.1590/0004-282X20190158.
Central nervous system (CNS) gliosarcoma (GSM) is a rare primary neoplasm characterized by the presence of glial and sarcomatous components.
In this report, we describe the clinical and neuroimaging aspects of three cases of GSM and correlate these aspects with pathological findings. We also provide a brief review of relevant literature.
Three patients were evaluated with magnetic resonance imaging (MRI), and biopsies confirmed the diagnosis of primary GSM, without previous radiotherapy.
The analysis of conventional sequences (T1, T1 after contrast injection, T2, Fluid attenuation inversion recovery, SWI and DWI/ADC map) and advanced (proton 1H MR spectroscopy and perfusion) revealed an irregular, necrotic aspect of the lesion, peritumoral edema/infiltration and isointensity of the solid component on a T2-weighted image. These features were associated with irregular and peripheral contrast enhancement, lipid and lactate peaks, increased choline and creatine levels in proton spectroscopy, increased relative cerebral blood volume (rCBV) in perfusion, multifocality and drop metastasis in one of the cases.
These findings are discussed in relation to the general characteristics of GSM reported in the literature.
中枢神经系统(CNS)胶质肉瘤(GSM)是一种罕见的原发性肿瘤,其特征是存在神经胶质和肉瘤成分。
在本报告中,我们描述了3例GSM患者的临床和神经影像学表现,并将这些表现与病理结果相关联。我们还对相关文献进行了简要综述。
对3例患者进行了磁共振成像(MRI)评估,活检证实为原发性GSM,之前未接受过放疗。
对常规序列(T1、注射造影剂后的T1、T2、液体衰减反转恢复序列、磁敏感加权成像和扩散加权成像/表观扩散系数图)以及高级序列(质子1H磁共振波谱和灌注成像)的分析显示,病变呈不规则、坏死状,瘤周水肿/浸润,T2加权像上实性成分呈等信号。这些特征与不规则及周边强化、脂质和乳酸峰、质子波谱中胆碱和肌酸水平升高、灌注成像中相对脑血容量(rCBV)增加、多灶性以及其中1例出现的脑脊液播散转移有关。
结合文献报道的GSM的一般特征对这些发现进行了讨论。