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后颅窝多形性胶质母细胞瘤:磁共振成像表现

Posterior fossa glioblastoma multiforme: MR findings.

作者信息

Kuroiwa T, Numaguchi Y, Rothman M I, Zoarski G H, Morikawa M, Zagardo M T, Kristt D A

机构信息

Department of Diagnostic Radiology, University of Maryland Medical System, Baltimore 21201, USA.

出版信息

AJNR Am J Neuroradiol. 1995 Mar;16(3):583-9.

Abstract

PURPOSE

To characterize the MR findings of glioblastoma multiforme in the posterior fossa.

METHODS

MR studies of nine patients with surgically proved posterior fossa glioblastoma multiforme were retrospectively evaluated. MR characteristics studied included tumor location, signal intensity, enhancement pattern, and presence of intratumoral hemorrhage, as well as presence of secondary hydrocephalus or metastatic spread.

RESULTS

The tumors were located in the median portion of the cerebellum or brain stem in eight cases. Six extended into the fourth ventricle. Hydrocephalus was seen in four cases. Six cases demonstrated decreased T1- and increased T2-weighted signal intensities. Three cases demonstrated mixed signal intensities suggesting intratumoral hemorrhage. All of the eight patients who received contrast showed moderate to marked heterogeneous ringlike enhancement suggesting intratumoral necrosis. Multicentric/multifocal lesions or extraaxial metastases were identified in three of the nine cases, and there was extracranial extension into the cervical region in one case.

CONCLUSION

Glioblastoma multiforme is a rare tumor in the posterior fossa. Differentiating it from metastatic tumor or malignant astrocytoma was difficult. However, combination of heterogeneous and ringlike enhancement, midline location, poorly defined margin, tumoral hemorrhage, concomitant multicentric/multifocal lesions, and extraaxial or extracranial metastasis may be clues for the prospective diagnosis of glioblastoma multiforme.

摘要

目的

描述后颅窝多形性胶质母细胞瘤的磁共振成像(MR)表现。

方法

回顾性评估9例经手术证实的后颅窝多形性胶质母细胞瘤患者的MR研究。研究的MR特征包括肿瘤位置、信号强度、强化模式、瘤内出血情况,以及是否存在继发性脑积水或转移扩散。

结果

8例肿瘤位于小脑或脑干的正中部位。6例延伸至第四脑室。4例可见脑积水。6例T1加权像信号减低,T2加权像信号增高。3例表现为混合信号强度,提示瘤内出血。接受对比剂检查的8例患者均显示中度至明显的不均匀环状强化,提示瘤内坏死。9例中有3例发现多中心/多灶性病变或轴外转移,1例病变向颈部颅外扩展。

结论

多形性胶质母细胞瘤在后颅窝是一种罕见肿瘤。将其与转移瘤或恶性星形细胞瘤鉴别困难。然而,不均匀和环状强化、中线位置、边界不清、肿瘤出血、并存多中心/多灶性病变以及轴外或颅外转移等表现相结合,可能为多形性胶质母细胞瘤的前瞻性诊断提供线索。

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