Department of Neuroradiology, San Camillo Forlanini Hospital, Rome, Italy.
Department of Neuroradiology, San Bortolo Hospital, Vicenza, Italy.
Radiol Med. 2021 Nov;126(11):1468-1476. doi: 10.1007/s11547-021-01401-4. Epub 2021 Aug 2.
The aim of this study was to report our experience with early stage glioblastoma (e-GB) and to investigate the possible clinical and imaging features that may be helpful to the radiologist to correctly diagnose this entity.
We performed a retrospective research of patients diagnosed with glioblastoma at two hospitals during a 10-year period. We reviewed all pre-operative MR and included only patients with early stage GB lesions, characterized by hyperintense on T2-weighted signal, with or without contrast-enhancement at post-contrast T1-weighted images, without "classic" imaging appearance of GB (necrosis, haemorrhage, oedema). All preoperative MR were evaluated by an experienced neuroradiologist and information on patients' demographics, clinical presentation, follow-up, and histopathology results study were collected. When available, preoperative CT examination was also evaluated.
We found 14 e-GBs in 13 patients (9 males, 4 females, median age 63 years) among 660 patients diagnosed with GB between 2010 and 2020. In 10 lesions, serial imaging revealed the transformation of e-GB in classic glioblastoma in a median time of 3 months. Clinical presentation included stroke-like symptoms, vertigo, seizures and confusion. Preoperative plain CT was performed in 8/13 cases and in 7 e-GBs presented as a hyperdense lesion. Ten out of 14 lesions transformed in classic GB before surgical intervention or biopsy. All lesions revealed typical immunohistochemical pattern of primary glioblastoma.
E-GB is a rare entity that can often lead to misdiagnosis. However, the radiologist should be aware of its imaging appearance to suggest the diagnosis and to request close imaging follow-up, hopefully improving the prognosis of this very aggressive disease.
本研究旨在报告我们在早期胶质母细胞瘤(e-GB)方面的经验,并探讨可能有助于放射科医生正确诊断该疾病的临床和影像学特征。
我们对两家医院在 10 年内诊断为胶质母细胞瘤的患者进行了回顾性研究。我们回顾了所有术前磁共振成像(MRI),并仅纳入具有早期 GB 病变的患者,这些病变在 T2 加权信号上呈高信号,在增强后 T1 加权图像上有或没有增强,没有“典型”的 GB 影像学表现(坏死、出血、水肿)。所有术前 MRI 均由经验丰富的神经放射科医生进行评估,并收集了患者的人口统计学、临床表现、随访和组织病理学结果研究的信息。如有可能,还评估了术前 CT 检查。
我们在 2010 年至 2020 年间诊断的 660 例胶质母细胞瘤患者中发现了 13 例患者(9 名男性,4 名女性,中位年龄 63 岁)中的 14 例 e-GB。在 10 个病变中,连续影像学显示 e-GB 在中位时间 3 个月内转变为典型的胶质母细胞瘤。临床表现包括类似中风的症状、眩晕、癫痫发作和意识混乱。术前平扫 CT 检查在 8/13 例中进行,在 7 例 e-GB 中表现为高密度病变。在手术干预或活检前,10 例病变转变为典型的胶质母细胞瘤。所有病变均显示原发性胶质母细胞瘤的典型免疫组织化学模式。
e-GB 是一种罕见的实体,往往会导致误诊。然而,放射科医生应该了解其影像学表现,以提示诊断,并要求进行密切的影像学随访,希望改善这种非常侵袭性疾病的预后。