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室管膜下瘤:临床与影像学特征分析

Subependymomas: an analysis of clinical and imaging features.

作者信息

Ragel Brian T, Osborn Anne G, Whang Kum, Townsend Jeannette J, Jensen Randy L, Couldwell William T

机构信息

Department of Neurosurgery, University of Utah, and Huntsman Cancer Institute, Salt Lake City 84132, USA.

出版信息

Neurosurgery. 2006 May;58(5):881-90; discussion 881-90. doi: 10.1227/01.NEU.0000209928.04532.09.

Abstract

OBJECTIVE

Subependymomas are slow-growing, benign tumors usually found incidentally in the fourth ventricle at autopsy. They are typically associated with the ventricular system and become apparent clinically only when symptoms of hydrocephalus or mass effect develop. We review clinical, histological, and contemporary radiographic presentations of 16 subependymomas, including 2 intraparenchymal tumors.

METHODS

We retrospectively evaluated eight patients with pathologically proven subependymomas. Initial magnetic resonance imaging and magnetic resonance spectroscopy were reviewed when available. Imaging was also available on eight outside subependymoma cases reviewed by our radiology department.

RESULTS

Twelve of these subependymomas were intraventricular, one was in the posterior fossa, two were intraparenchymal, and one was an intramedullary spinal cord tumor. These lesions were hypo- to hyperintense on T1- and T2-weighted magnetic resonance imaging, with minimal to moderate enhancement. Initial complaints included headache, seizures, tingling sensations, and weakness. Among our eight patients who underwent gross total resection with no adjuvant therapy, no recurrences have been noted on follow-up magnetic resonance imaging.

CONCLUSION

Subependymomas are rare, representing only 0.51% of all central nervous system tumors operated on during an 8-year period at the University of Utah. Clinical symptoms were associated with tumor location: intracranial masses caused headaches, seizures, and neurological complaints, and spinal cord locations resulted in neurological deficit. The authors review the clinical presentation, management, and contemporary radiographic appearance of this rare tumor.

摘要

目的

室管膜下瘤是生长缓慢的良性肿瘤,通常在尸检时偶然发现于第四脑室。它们通常与脑室系统相关,只有在出现脑积水或占位效应症状时才会在临床上显现出来。我们回顾了16例室管膜下瘤的临床、组织学和现代影像学表现,其中包括2例脑实质内肿瘤。

方法

我们回顾性评估了8例经病理证实的室管膜下瘤患者。如有可用的初始磁共振成像和磁共振波谱检查结果也进行了回顾。我们放射科还对另外8例室管膜下瘤病例的影像学资料进行了评估。

结果

这些室管膜下瘤中,12例位于脑室内,1例位于后颅窝,2例位于脑实质内,1例为脊髓髓内肿瘤。这些病变在T1加权和T2加权磁共振成像上呈低信号至高信号,强化程度轻微至中等。初始症状包括头痛、癫痫发作、刺痛感和无力。在我们8例接受了全切除且未进行辅助治疗的患者中,随访磁共振成像未发现复发。

结论

室管膜下瘤较为罕见,在犹他大学8年期间接受手术的所有中枢神经系统肿瘤中仅占0.51%。临床症状与肿瘤位置相关:颅内肿块引起头痛、癫痫发作和神经症状,脊髓部位则导致神经功能缺损。作者回顾了这种罕见肿瘤的临床表现、治疗及现代影像学表现。

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