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结节性硬化症中的室管膜下巨细胞星形细胞瘤:内镜图像及对治疗的启示

Subependymal giant-cell astrocytoma in tuberous sclerosis: endoscopic images and the implications for therapy.

作者信息

Beems T, Grotenhuis J A

机构信息

Department of Neurosurgery, Academic Hospital St. Radboud, Nijmegen, The Netherlands.

出版信息

Minim Invasive Neurosurg. 2001 Mar;44(1):58-60. doi: 10.1055/s-2001-13580.

Abstract

Supratentorial intraventricular tumors are not frequently encountered in childhood. One of the most frequent intraventricular glial tumors is the subependymal giant-cell astrocytoma, mostly associated with tuberous sclerosis. These tumors are diagnosed on computed tomography (CT) or magnetic resonance imaging (MRI) scans. They can occur isolated or multiple and operative resection is advised if these tumors cause symptoms, usually raised intracranial pressure due to obstructive hydrocephalus. However, the number of tumors can be much higher than seen on radiological examination making total resection of all tumors impossible. We demonstrate this with the endoscopic images derived during the endoscopic removal of a subependymal giant-cell astrocytoma obstructing a foramen of Monro in a 15-year-old boy with tuberous sclerosis.

摘要

幕上脑室肿瘤在儿童时期并不常见。最常见的脑室胶质肿瘤之一是室管膜下巨细胞星形细胞瘤,大多与结节性硬化症相关。这些肿瘤通过计算机断层扫描(CT)或磁共振成像(MRI)扫描得以诊断。它们可以孤立出现或多发,如果这些肿瘤引起症状,通常是由于梗阻性脑积水导致颅内压升高,建议进行手术切除。然而,肿瘤的数量可能比影像学检查所见的要多得多,这使得完全切除所有肿瘤变得不可能。我们通过一名患有结节性硬化症的15岁男孩在进行内镜下切除阻塞Monro孔的室管膜下巨细胞星形细胞瘤过程中获取的内镜图像来证明这一点。

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