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早期胶质母细胞瘤:临床和影像学特征的回顾性多中心分析。

Early stage glioblastoma: retrospective multicentric analysis of clinical and radiological features.

机构信息

Department of Neuroradiology, San Camillo Forlanini Hospital, Rome, Italy.

Department of Neuroradiology, San Bortolo Hospital, Vicenza, Italy.

出版信息

Radiol Med. 2021 Nov;126(11):1468-1476. doi: 10.1007/s11547-021-01401-4. Epub 2021 Aug 2.

Abstract

OBJECTIVES

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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