Otomo Mayuko, Kanamori Masayuki, Sato Shiho, Shimoda Yoshiteru, Watanabe Mika, Kawaguchi Tomohiro, Saito Ryuta, Tominaga Teiji
Department of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, JPN.
Department of Diagnostic Radiology, Tohoku University Graduate School of Medicine, Sendai, JPN.
Cureus. 2023 Feb 6;15(2):e34672. doi: 10.7759/cureus.34672. eCollection 2023 Feb.
Glioblastoma sometimes develops with acute onset due to intracerebral hemorrhage. Although it is sometimes difficult to diagnose patients with hemorrhagic-onset glioblastoma at the acute phase of intracerebral hemorrhage (ICH), the progressive enlargement of perifocal edema or the development of contrast-enhanced lesion triggers the diagnosis of glioblastoma within six months. Herein, we present a rare case of glioblastoma in which the diagnosis was delayed as long as 17 months after ICH. A 62-year-old man presented with a headache and aphasia. Computed tomography revealed ICH in the left temporal lobe. Magnetic resonance (MR) images revealed that the hematoma had a mix of isointense and surrounding hypointense lesions on T1-weighted MR images and gadolinium-enhanced lesions at the wall and the septum of the hematoma. An endoscopic evacuation of the hematoma was performed. No causative lesions were found during intraoperative and histological examinations. After seven months, abnormal signals were completely resolved on MR images, except for the small and stable enhanced lesion on three-dimensional gadolinium-enhanced T1-weighted MR imaging (3D Gd-T1WI) at the base of the hematoma, which did not change in size for seven months. However, a large gadolinium-enhanced lesion at the left temporal lobe developed 17 months after ICH. He underwent total resection of the lesion and was diagnosed with glioblastoma. He received radiation therapy and temozolomide but died of disseminated recurrence 31 months after ICH. In conclusion, this report presents a didactic case of glioblastoma in which the diagnosis of glioblastoma was delayed 17 months after ICH whereas hemorrhagic-onset glioblastoma was previously considered ruled out in cases in which six months or more have passed after ICH. In order not to overlook these cases, follow-up with 3D Gd-T1WI is essential in the case of suspected tumor-related ICH and close follow-up is recommended when the enhanced lesion does not resolve after a long period even if it does not grow.
胶质母细胞瘤有时会因脑出血而急性起病。尽管在脑出血(ICH)急性期诊断出血性起病的胶质母细胞瘤患者有时很困难,但病灶周围水肿的逐渐扩大或强化病灶的出现会促使在六个月内诊断出胶质母细胞瘤。在此,我们报告一例罕见的胶质母细胞瘤病例,其诊断在脑出血后长达17个月才得以确定。一名62岁男性出现头痛和失语症状。计算机断层扫描显示左颞叶脑出血。磁共振(MR)图像显示,血肿在T1加权MR图像上有等信号和周围低信号混合病灶,且在血肿壁和间隔处有钆强化病灶。进行了血肿的内镜清除术。术中及组织学检查未发现病因性病灶。七个月后,除血肿底部在三维钆增强T1加权MR成像(3D Gd-T1WI)上有小而稳定的强化病灶且七个月大小未变外,MR图像上的异常信号已完全消失。然而,脑出血17个月后左颞叶出现一个大的钆强化病灶。他接受了病灶全切术并被诊断为胶质母细胞瘤。他接受了放疗和替莫唑胺治疗,但在脑出血31个月后死于播散性复发。总之,本报告展示了一例有教育意义的胶质母细胞瘤病例,其中胶质母细胞瘤的诊断在脑出血后延迟了17个月,而此前认为在脑出血后六个月或更长时间的病例中可排除出血性起病的胶质母细胞瘤。为了不遗漏这些病例,对于疑似肿瘤相关的脑出血病例,进行3D Gd-T1WI随访至关重要,并且当强化病灶即使不增大但长期不消退时,建议密切随访。