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42例颅底脊索瘤和软骨肉瘤的放射学特征与组织病理学相关性分析。

Analysis of radiological features relative to histopathology in 42 skull-base chordomas and chondrosarcomas.

作者信息

Pamir M Necmettin, Ozduman Koray

机构信息

Department of Neurosurgery, Marmara University Faculty of Medicine, Istanbul, Turkey.

出版信息

Eur J Radiol. 2006 Jun;58(3):461-70. doi: 10.1016/j.ejrad.2006.03.020. Epub 2006 May 2.

Abstract

Chordomas and chondrosarcomas are malignant tumors that are reported to have similar clinical presentations and radiological features but different behaviors and outcomes. The aim of this retrospective study was to determine whether specific radiological features of skull-base chordomas or chondrosarcomas are correlated with histopathology, and thus allow preoperative diagnosis. The study involved 32 classic chordomas, 6 chondroid chordomas and 4 chondrosarcomas (42 tumors total). For each case, tumor size and extent, the detailed anatomy involved, and magnetic resonance imaging and computed tomography findings were analyzed. Tumor extent was assessed using a novel method that assessed presence/absence in 18 defined skull-base zones. The chondrosarcomas presented significantly earlier in life than the chordomas (means, 20.5 years versus 36 years, respectively). At time of diagnosis, the median tumor volume was 23 cm(3) (range, 1.2-78.8 cm(3)) and the mean tumor extent was 6.7+/-2.9 zones. There were no differences between chordomas and chondrosarcomas, or between the two chordoma subgroups, with respect to lesion volume or extent. Comparison of other imaging findings revealed no features that were diagnostic for either chordoma or chondrosarcoma. The data support previous claims that chondrosarcomas present earlier in life than chordomas, but this finding is not diagnostic. There is wide variation in the extent of skull-base chordomas and chondrosarcomas, and in the specific anatomical structures these tumors involve. None of the MRI or CT features of these tumors appear to be useful for differentiating chordomas from chondrosarcomas preoperatively. For surgical planning, specific, area-oriented definition of tumor extent might provide more useful information than tumor-type classification schemes.

摘要

脊索瘤和软骨肉瘤是恶性肿瘤,据报道它们具有相似的临床表现和放射学特征,但行为和预后不同。这项回顾性研究的目的是确定颅底脊索瘤或软骨肉瘤的特定放射学特征是否与组织病理学相关,从而实现术前诊断。该研究纳入了32例经典脊索瘤、6例软骨样脊索瘤和4例软骨肉瘤(共42个肿瘤)。对每例病例的肿瘤大小和范围、所累及的详细解剖结构以及磁共振成像和计算机断层扫描结果进行了分析。使用一种新方法评估肿瘤范围,该方法评估18个定义的颅底区域中肿瘤的存在与否。软骨肉瘤的发病年龄明显早于脊索瘤(平均年龄分别为20.5岁和36岁)。在诊断时,肿瘤体积中位数为23 cm³(范围为1.2 - 78.8 cm³),平均肿瘤范围为6.7±2.9个区域。脊索瘤和软骨肉瘤之间,以及两个脊索瘤亚组之间,在病变体积或范围方面没有差异。对其他影像学表现的比较未发现可诊断脊索瘤或软骨肉瘤的特征。这些数据支持了之前关于软骨肉瘤发病年龄早于脊索瘤的说法,但这一发现并无诊断价值。颅底脊索瘤和软骨肉瘤的范围以及它们所累及的特定解剖结构存在很大差异。这些肿瘤的磁共振成像或计算机断层扫描特征似乎都无助于术前区分脊索瘤和软骨肉瘤。对于手术规划而言,基于特定区域的肿瘤范围定义可能比肿瘤类型分类方案提供更有用的信息。

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