Department of Orthopedics and Physical Rehabilitation, University of Massachusetts Memorial Medical Center, Worchester, MA, USA.
J Am Acad Orthop Surg. 2010 Jun;18(6):358-66. doi: 10.5435/00124635-201006000-00008.
Osteofibrous dysplasia (OFD) is a rare, benign, fibro-osseous lesion that typically is seen within the cortex of the tibia in children. Adamantinoma (AD) is a rare, low-grade malignant primary bone tumor that occurs most often in the tibia and/or fibula of adolescent persons and young adults; however, it has been reported in other long bones, as well. Immunohistochemical and ultrastructural evidence has shown that the neoplastic cell in AD derives from an epithelial lineage. More recently, published reports have described another clinical entity-differentiated or OFD-like AD-that appears to lie between OFD and AD along a spectrum of disease. Controversy exists as to whether OFD is a precursor lesion to AD or whether OFD may be a residual lesion resulting from a spontaneously regressing AD. Management of OFD varies from observation to surgical intervention, depending on the age of the patient and the extent of the lesion. Management of AD requires surgical resection with wide margins, followed by appropriate reconstruction, to minimize the risk of local recurrence or metastasis.
骨纤维结构不良(OFD)是一种罕见的良性纤维骨病变,通常发生在儿童胫骨皮质内。造釉细胞瘤(AD)是一种罕见的低度恶性原发性骨肿瘤,最常发生在青少年和年轻成年人的胫骨和/或腓骨;然而,它也已在其他长骨中报道过。免疫组化和超微结构证据表明,AD 中的肿瘤细胞来源于上皮谱系。最近,发表的报告描述了另一种临床实体——分化型或 OFD 样 AD——它似乎沿着疾病谱位于 OFD 和 AD 之间。关于 OFD 是否是 AD 的前驱病变,或者 OFD 是否可能是自发消退的 AD 遗留的病变,存在争议。OFD 的治疗因患者年龄和病变范围而异,从观察到手术干预不等。AD 的治疗需要广泛切除肿瘤,然后进行适当的重建,以最大程度地降低局部复发或转移的风险。