对颅底偶然出现的良性脊索瘤病变采取观察、等待和重新扫描的方法

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Inga E. Usher, Evangelos Drosos, Abdalla Morsy, Andrea Wadeson, Roger Laitt, Sarah Abdulla, Aparna Madhavan, Jane Halliday, Scott Rutherford, Andrew T. King, Omar N. Pathmanaban
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引用次数: 0

摘要

目的:本研究旨在描述颅底偶发良性脊索瘤病变的自然病史,特别关注那些可能导致与低级别脊索瘤更难鉴别的特征,即对比剂摄取和骨侵蚀。方法在这一回顾性病例系列中,作者描述了 58 例颅底偶然出现的良性脊索瘤病变患者的临床结果,包括那些具有骨侵蚀或造影剂摄取等轻微放射学特征的患者。结果在近 3 年的中位随访期间,所有病变均保持稳定。37例(64%)患者接受了造影剂增强磁共振成像检查;其中14例(38%)患者的病变显示出最小的造影剂增强。结论:这些数据表明,即使造影剂摄取较少或骨侵蚀程度较轻,也应首先对某些看似良性的梭形细胞病变病例进行监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A watch, wait, and rescan approach for incidental benign-appearing notochordal lesions of the skull base
OBJECTIVE

The aim of this study was to describe the natural history of incidental benign-appearing notochordal lesions of the skull base with specific attention to features that can make differentiation from low-grade chordoma more difficult, namely contrast uptake and bone erosion.

METHODS

In this retrospective case series, the authors describe the clinical outcomes of 58 patients with incidental benign-appearing notochordal lesions of the clivus, including those with minor radiological features of bone erosion or contrast uptake.

RESULTS

All lesions remained stable during a median follow-up of almost 3 years. Thirty-seven (64%) patients underwent contrast-enhanced MRI; lesions in 14 (38%) of these patients exhibited minimal contrast enhancement. Twenty-seven (47%) patients underwent CT; lesions in 6 (22%) of these patients exhibited minimal bone erosion.

CONCLUSIONS

These data make the case for monitoring selected cases of benign-appearing notochordal lesions of the clivus in the first instance even when there is minor contrast uptake or minimal bone erosion.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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