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Juvenile trabecular ossifying fibroma: an update

机译:少年小梁骨化性纤维瘤:最新进展

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摘要

Fibro-osseous lesions are characterized by the presence of bone marrow that has changed into fibrous tissue and that contains mineralized material of varying appearances. Because of overlapping clinical, radiological, and histopathological features, their classification has evoked much discussion. The current classification recognizes fibrous dysplasia, ossifying fibroma, and osseous dysplasia. Juvenile trabecular ossifying fibroma is a rare variant of ossifying fibroma that is clinically characterized by rapid growth that may suggest malignancy. A series of 15 cases is reported with emphasis on a hitherto unnoticed histological feature that may be helpful in recognizing this lesion.
机译:纤维性骨病变的特征是存在骨髓,该骨髓已变成纤维组织,并包含外观各异的矿物质。由于临床,放射学和组织病理学特征重叠,它们的分类引起了很多讨论。当前的分类可识别纤维不典型增生,骨化纤维瘤和骨不典型增生。少年小梁性骨化性纤维瘤是骨化性纤维瘤的一种罕见变体,临床上的特征是生长迅速,可能提示恶性。报告了一系列15例病例,重点是迄今为止尚未发现的组织学特征,可能有助于识别该病变。

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