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酷似病因不明的蛛网膜下腔出血的胶质母细胞瘤:一例报告

Glioblastoma Mimicking Subarachnoid Hemorrhage of Unknown Etiology: A Case Report.

作者信息

Matsuda Ryosuke, Nakamura Mitsutoshi, Tanaka Yoshitaka, Takamura Yoshiaki, Nakagawa Ichiro, Motoyama Yasushi

机构信息

Department of Neurosurgery, Nara Medical University, Kashihara, Japan.

Department of Neurosurgery, Nara Medical University, Kashihara, Japan.

出版信息

World Neurosurg. 2018 Dec;120:54-58. doi: 10.1016/j.wneu.2018.08.149. Epub 2018 Aug 29.

Abstract

BACKGROUND

Glioblastoma is the most common primary malignant tumor of the brain. Common radiologic findings using initial computed tomography (CT) reveal an intra-axial lesion with perifocal edema. Here, we present a rare case of diffuse subarachnoid hemorrhage (SAH) detected on an initial CT image in a patient without intracranial aneurysm in whom the final diagnosis was glioblastoma.

CASE DESCRIPTION

We report the rare case of a 57-year-old man with glioblastoma in the right temporal lobe who presented with a sudden onset of disturbance of consciousness as an initial manifestation. Initial CT of the head revealed a diffuse SAH. Digital subtraction angiography revealed no cerebral aneurysm or dissection of intracranial arteries. The patient was treated for SAH of unknown etiology with conservative therapy, and a repeat digital subtraction angiography demonstrated no vascular disease. Eventually, he was discharged without any neurologic deficit. A follow-up CT of the brain revealed an intracerebral hemorrhage in the right temporal lobe, and magnetic resonance imaging revealed a ring enhancing lesion in the anterior section of right temporal lobe. The patient was transferred to our department, where he underwent surgical resection, and a pathologic diagnosis of glioblastoma was made.

CONCLUSIONS

We present a rare case of glioblastoma mimicking SAH of unknown etiology and recommend including glioblastoma in the differential diagnosis of SAH of unknown etiology.

摘要

背景

胶质母细胞瘤是最常见的原发性脑恶性肿瘤。初次计算机断层扫描(CT)的常见影像学表现为轴内病变伴灶周水肿。在此,我们报告一例罕见病例,一名最终诊断为胶质母细胞瘤的患者在初次CT图像上检测到弥漫性蛛网膜下腔出血(SAH),且无颅内动脉瘤。

病例描述

我们报告一例罕见病例,一名57岁男性,右颞叶胶质母细胞瘤,最初表现为突发意识障碍。头部初次CT显示弥漫性SAH。数字减影血管造影未发现脑动脉瘤或颅内动脉夹层。该患者因病因不明的SAH接受保守治疗,重复数字减影血管造影未显示血管疾病。最终,他出院时无任何神经功能缺损。脑部随访CT显示右颞叶脑出血,磁共振成像显示右颞叶前部环形强化病变。患者转至我科,接受手术切除,病理诊断为胶质母细胞瘤。

结论

我们报告一例罕见的胶质母细胞瘤病例,其表现类似病因不明的SAH,并建议在病因不明的SAH鉴别诊断中考虑胶质母细胞瘤。

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