Ghaderi Sadegh, Mohammadi Sana, Hoseini Pourasl Masoud, Fatehi Farzad
Neuromuscular Research Center, Department of Neurology, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran; Department of Neuroscience and Addiction Studies, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Neuromuscular Research Center, Department of Neurology, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran; Department of Medical Sciences, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Int J Surg Case Rep. 2024 Jan;114:109152. doi: 10.1016/j.ijscr.2023.109152. Epub 2023 Dec 13.
Unlike children, high-grade brainstem glioma (HG-BSG) in adults is a rare and diverse group of tumors. They can be classified based on their location and physical characteristics, which distinguishes them from pediatric brainstem gliomas. They are rare in adults, constituting only 1 % to 2 % of intracranial gliomas. They are often aggressive and have a poor prognosis, with a median survival time of 24 months. The diagnosis of brainstem gliomas typically involves a combination of clinical evaluation and imaging studies, mainly magnetic resonance imaging (MRI), which provides detailed images and can help identify the characteristics of the tumor.
We present a case study of an uncommon presentation of an early stage of HG-BSG in a 33-year-old male, who had a contrast-enhancing lesion in the ventrolateral medulla that extended to the lower aspect of the fourth ventricle and caused ventricular compression.
The findings were consistent with the literature on the current state of HG-BSG MRI findings, which typically show contrast-enhancing, hyperintense, and infiltrative lesions that involve the pons, midbrain, or medulla oblongata. The diagnosis of HG-BSG was based on clinical and radiological criteria, as the patient refused to undergo a surgical biopsy. We also performed a literature review on the current state of brainstem HG-BSG MRI findings, summarizing the main features and patterns of these tumors.
MRI can offer useful information regarding the tumor's location, size, and features, as well as its impact on surrounding tissues and cerebrospinal fluid circulation.
与儿童不同,成人高级别脑干胶质瘤(HG-BSG)是一组罕见且多样的肿瘤。它们可根据位置和物理特征进行分类,这使其有别于小儿脑干胶质瘤。它们在成人中很罕见,仅占颅内胶质瘤的1%至2%。它们通常具有侵袭性,预后较差,中位生存时间为24个月。脑干胶质瘤的诊断通常涉及临床评估和影像学检查相结合,主要是磁共振成像(MRI),它能提供详细图像并有助于识别肿瘤特征。
我们报告一例33岁男性HG-BSG早期罕见表现的病例研究,该患者延髓腹外侧有一个强化病灶,延伸至第四脑室下部并导致脑室受压。
这些发现与关于HG-BSG MRI表现现状的文献一致,其通常显示累及脑桥、中脑或延髓的强化、高信号和浸润性病灶。由于患者拒绝接受手术活检,HG-BSG的诊断基于临床和放射学标准。我们还对脑干HG-BSG MRI表现现状进行了文献综述,总结了这些肿瘤的主要特征和模式。
MRI可提供有关肿瘤位置、大小、特征以及其对周围组织和脑脊液循环影响的有用信息。