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一例硬化性骨肉瘤中基质矿化的改变。

Altered matrix mineralization in a case of a sclerosing osteosarcoma.

机构信息

Department of Orthopaedic Surgery, Vienna General Hospital, Medical University of Vienna, Vienna, Austria.

出版信息

Bone. 2013 Apr;53(2):409-13. doi: 10.1016/j.bone.2012.12.043. Epub 2013 Jan 2.

Abstract

Little is known about the tumor matrix mineralization of highly sclerotic osteosarcoma. We used quantitative backscattered electron imaging (qBEI) to determine the Bone mineralization density distribution (BMDD) of a highly sclerosing osteosarcoma of the proximal tibia as well as adjacent normal bone of a 10-year-old girl following chemotherapy according to the EURAMOS-1 protocol. Data were compared to recently published normative reference data for young individuals. Backscattered electron imaging of the tumor region revealed a dense accumulation of mineralized tumor bone matrix (up to 90% of the medullar space). The BMDD was shifted tremendously towards higher matrix mineralization (CaMean +18.5%, CaPeak +22.5%, CaHigh +100 fold) compared to normal bone. Additionally the BMDD became much wider, indicating a higher heterogeneity in mineralization (CaWidth +40%). In contrast to lamellar bone, which mineralizes via a mineralization front, the mineralization of the tumor matrix starts by randomly distributed spots of mineral clusters fusing together to a highly mineralized non-lamellar bone matrix. We also found an altered BMDD of the patient's normal bone when compared with the reference BMDD of young individuals. In conclusion this high radiodensity region of the sclerosing sarcoma is not only due to the high amount of tumor matrix but also to its high mineralization density. Chemotherapy may lead to altered matrix mineralization of normal bone due to suppression of bone turnover. The mechanism of matrix mineralization in a sclerosing osteosarcoma warrants further studies.

摘要

关于高度硬化性骨肉瘤的肿瘤基质矿化,人们知之甚少。我们根据 EURAMOS-1 方案,使用定量背散射电子成像(qBEI)来确定一名 10 岁女孩化疗后胫骨近端高度硬化性骨肉瘤以及相邻正常骨的骨矿物质化密度分布(BMDD)。数据与最近公布的年轻人正常参考数据进行了比较。肿瘤区域的背散射电子成像显示矿化肿瘤骨基质的密集堆积(高达髓腔的 90%)。与正常骨相比,BMDD 向更高的基质矿化(CaMean+18.5%,CaPeak+22.5%,CaHigh+100 倍)发生了巨大的偏移。此外,BMDD 变得更宽,表明矿化的异质性更高(CaWidth+40%)。与通过矿化前缘矿化的板层骨不同,肿瘤基质的矿化始于随机分布的矿化簇点融合在一起,形成高度矿化的非板层骨基质。与年轻人的正常骨参考 BMDD 相比,我们还发现患者正常骨的 BMDD 发生了改变。总之,硬化性肉瘤的这种高放射密度区域不仅是由于肿瘤基质的大量存在,还由于其高矿化密度。化疗可能会导致正常骨的基质矿化发生改变,原因是骨转换受到抑制。硬化性骨肉瘤基质矿化的机制需要进一步研究。

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