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儿童恶性脊髓星形细胞瘤的磁共振成像特征

MR characteristics of malignant spinal cord astrocytomas in children.

作者信息

Kulkarni A V, Armstrong D C, Drake J M

机构信息

Division of Neurosurgery, Hospital for Sick Children, University of Toronto, Canada.

出版信息

Can J Neurol Sci. 1999 Nov;26(4):290-3. doi: 10.1017/s0317167100000408.

Abstract

OBJECTIVE

Malignant spinal cord astrocytomas are rare tumors and their specific MR characteristics have not been previously described. We present a detailed MR analysis of four children with malignant astrocytoma.

METHODS

A review of the clinical database at the Hospital for Sick Children, Toronto revealed four patients with histologically-verified malignant spinal cord astrocytomas (WHO Grade 3 or 4) with pre-operative MR available for retrospective review.

RESULTS

There were three boys and one girl with a mean age at presentation of four years (range 7 months-12 years). Mean duration of symptoms prior to presentation was six weeks (range 3 days-5 months). Pre-operative MR analysis revealed that all tumors were located in the cervical or cervico-thoracic regions and expanded the cord over an average of 6.5 vertebral levels. The signal was usually hypointense on T1-weighted and hyperintense or mixed intensity on T2-weighted images. In the three cases where gadolinium was given, all demonstrated enhancement (one rim enhancement with a discrete border and two with inhomogeneous central enhancement). One tumor appeared to be exophytic, one had a significant cystic component, and none showed evidence of hemorrhage. Pre-operative leptomeningeal spread of tumor was documented in two of four cases and involved intracranial spread in both cases.

CONCLUSIONS

There did not appear to be any specific MR characteristics to help differentiate a malignant astrocytoma from a low-grade tumor, except for the high rate of leptomeningeal spread at presentation. It is recommended that full neuraxis MR imaging be performed pre-operatively in children in whom a rapidly progressive clinical course suggests a malignant lesion. This will likely have a high positive yield and provide valuable information prior to surgical intervention.

摘要

目的

恶性脊髓星形细胞瘤是罕见肿瘤,其特定的磁共振成像(MR)特征此前尚未见报道。我们对4例恶性星形细胞瘤患儿进行了详细的MR分析。

方法

回顾多伦多病童医院的临床数据库,发现4例经组织学证实的恶性脊髓星形细胞瘤(世界卫生组织3级或4级)患者,其术前MR图像可供回顾性分析。

结果

3例男孩和1例女孩,就诊时平均年龄为4岁(范围7个月至12岁)。就诊前症状的平均持续时间为6周(范围3天至5个月)。术前MR分析显示,所有肿瘤均位于颈段或颈胸段,脊髓平均受累6.5个椎体节段。T1加权像上信号通常为低信号,T2加权像上为高信号或混合信号。在3例使用钆剂增强的病例中,均显示强化(1例为边缘强化,边界清晰,2例为中央不均匀强化)。1例肿瘤呈外生性,1例有明显的囊性成分,均未显示出血迹象。4例中有2例记录到术前肿瘤软脑膜播散,且2例均有颅内播散。

结论

除就诊时软脑膜播散率高外,似乎没有任何特定的MR特征有助于将恶性星形细胞瘤与低级别肿瘤区分开来。建议对于临床病程快速进展提示为恶性病变的儿童,术前进行全神经轴MR成像。这可能会有很高的阳性检出率,并在手术干预前提供有价值的信息。

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