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后颅窝神经节胶质瘤

Posterior cranial fossa gangliogliomas.

作者信息

Safavi-Abbasi Sam, Di Rocco Federico, Chantra Kraisri, Feigl Guenther C, El-Shawarby Amr, Samii Amir, Samii Madjid

机构信息

Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona.

出版信息

Skull Base. 2007 Jul;17(4):253-64. doi: 10.1055/s-2007-984486.

Abstract

Ganglioglioma (GG) is an uncommon primary lesion of the central nervous system that is typically located supratentorially. There are only a few reports of GG arising from the cerebellum. To the best of our knowledge this is the first case of a cerebellar GG with supratentorial extension and a longstanding history before its recognition. In fact, this 29-year-old male presented with an 11-year history of intermittent headaches. A cranial computerized tomography (CT) performed at the onset of his complaints failed to reveal the tumor. After a particularly longstanding cephalalgic episode, the patient underwent a new CT scan that was also negative. However, magnetic resonance (MR) imaging of the brain revealed a space-occupying lesion in the right cerebellar hemisphere with extension to the level of the superior colliculi and pineal recess. The tumor was partially removed through a midline suboccipital craniotomy and supracerebellar approach. Pathological examination of the tumor showed composition of atypical ganglion cells and astrocytes, indicating the diagnosis of cerebellar GG. At last follow-up, 24 months after surgery, the patient reported a marked improvement of his clinical condition with significant reduction of intensity and frequency of the headache. The present report illustrates how cerebellar GG may remain undetectable by CT and may therefore present with a longstanding history and nonspecific signs and symptoms. MR investigation can lead to the proper diagnosis. Even after partial removal the prognosis remains good and remission of the symptoms may be achieved. In this article, we review the literature and summarize the current understanding of infratentorial GGs.

摘要

节细胞胶质瘤(GG)是一种罕见的中枢神经系统原发性病变,通常位于幕上。仅有少数关于起源于小脑的GG的报道。据我们所知,这是首例具有幕上扩展且在确诊前有长期病史的小脑GG。事实上,这位29岁男性有11年的间歇性头痛病史。在其主诉发作时进行的头颅计算机断层扫描(CT)未发现肿瘤。在一次特别漫长的头痛发作后,患者接受了新的CT扫描,结果也是阴性。然而,脑部磁共振成像(MR)显示右侧小脑半球有占位性病变,向上延伸至中脑上丘和松果体隐窝水平。通过枕下中线开颅和小脑上入路部分切除了肿瘤。肿瘤的病理检查显示由非典型神经节细胞和星形胶质细胞组成,提示诊断为小脑GG。在术后24个月的最后一次随访中,患者报告其临床状况有显著改善,头痛的强度和频率明显降低。本报告说明了小脑GG如何可能在CT检查中未被发现,因此可能表现为长期病史以及非特异性的体征和症状。MR检查可导致正确诊断。即使部分切除后,预后仍然良好,症状可能会缓解。在本文中,我们回顾了文献并总结了目前对幕下GG的认识。

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Posterior cranial fossa gangliogliomas.后颅窝神经节胶质瘤
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Ganglioglioma of the brainstem: report of three cases and review of the literature.
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