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难以区分良性脊索细胞瘤与脊索瘤这一情况进一步表明了它们之间的联系。

Difficulty distinguishing benign notochordal cell tumor from chordoma further suggests a link between them.

作者信息

Kreshak Jennifer, Larousserie Frédérique, Picci Piero, Boriani Stefano, Mirra Joseph, Merlino Biagio, Brunocilla Eugenio, Vanel Daniel

出版信息

Cancer Imaging. 2014 Apr 22;14(1):4. doi: 10.1186/1470-7330-14-4.

Abstract

BACKGROUND

Much discussion about benign notochordal cell tissue in vertebrae has centered on the nature of its relationship, if any, to chordoma. Often referred to as benign notochordal cell tumors (BNCTs), these lesions have unique morphological features, however, differentiating between notochordal cells in discs, BNCT, and chordoma can be difficult. They are described as radiologically distinct from chordoma, with lysis, contrast enhancement, and a soft tissue mass indicating chordoma.

METHODS

All chordomas diagnosed at our institution, the Istituto Ortopedico Rizzoli (Bologna, Italy), prior to 2008 were reviewed, yielding 174 cases. Five were limited to bone; one was a recurrent chordoma without original data available. The remaining four were re-evaluated in detail.

RESULTS

There were three women and one man, aged 33-57 years (mean, 48 years). Two were BNCTs and two were mixed lesions containing BNCT and chordoma. On computed tomography, all were radiopaque with areas of lysis. One BNCT was heterogeneous on magnetic resonance imaging, enhancing after contrast. Microscopically, one BNCT had a well-defined cystic area with a sclerotic border. The other had a minute atypical area; it recurred as chordoma. The mixed lesions had areas of definitive BNCT, definitive chordoma, and atypical areas that did not meet the criteria for either. The atypical areas in all three cases 'blended' with areas of chordoma or BNCT.

CONCLUSION

These cases illustrate the ongoing challenges in differentiating between BNCT and chordoma. All had unique imaging features; three had atypical microscopic areas blending with BNCT or chordoma, strengthening the argument for a relationship between the two entities and supporting the idea that some BNCTs may progress to chordoma. Our study dispels the notion that any single radiologic criterion used to distinguish between chordoma and BNCT is reliable, opening the discussion as to whether or how to monitor BNCTs.

摘要

背景

关于椎体内良性脊索细胞组织的诸多讨论都聚焦于其与脊索瘤之间的关系本质(若存在关系的话)。这些病变常被称为良性脊索细胞瘤(BNCT),具有独特的形态学特征,然而,区分椎间盘内的脊索细胞、BNCT和脊索瘤可能存在困难。它们在影像学上被描述为与脊索瘤不同,骨质溶解、对比增强以及软组织肿块提示为脊索瘤。

方法

对2008年前在我们机构——意大利博洛尼亚的里佐利骨科研究所诊断的所有脊索瘤进行回顾,共174例。5例局限于骨骼;1例为复发性脊索瘤,无原始数据。其余4例进行了详细的重新评估。

结果

有3名女性和1名男性,年龄33 - 57岁(平均48岁)。2例为BNCT,2例为包含BNCT和脊索瘤的混合性病变。在计算机断层扫描上,所有病变均表现为不透光且伴有骨质溶解区域。1例BNCT在磁共振成像上表现为不均匀,对比增强后强化。显微镜下,1例BNCT有边界清晰的囊性区域且边界硬化。另1例有微小的非典型区域;复发时为脊索瘤。混合性病变有明确的BNCT区域、明确的脊索瘤区域以及不符合两者标准的非典型区域。所有3例中的非典型区域都与脊索瘤或BNCT区域“融合”。

结论

这些病例说明了在区分BNCT和脊索瘤方面持续存在的挑战。所有病例都有独特的影像学特征;3例有与BNCT或脊索瘤融合的非典型显微镜下区域,这强化了两者之间存在关联的观点,并支持了一些BNCT可能进展为脊索瘤的观点。我们的研究消除了用于区分脊索瘤和BNCT的任何单一放射学标准是可靠的这一观念,开启了关于是否以及如何监测BNCT的讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e4a/4212531/55f744e104db/1470-7330-14-4-1.jpg

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