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Osteonecrosis of the jaw: who gets it, and why?

机译:颌骨坏死:谁得到的,为什么?

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摘要

Osteonecrosis of the jaw (ONJ) is now defined by the presence of exposed bone in the mouth, which fails to heal after appropriate intervention over a period of six or eight weeks. It is commonly precipitated by a tooth extraction in patients treated with zoledronate, pamidronate or a combination of these agents, for the management of myeloma, breast cancer or prostate cancer. In patients with these malignancies who are treated with bisphosphonates, the overall prevalence is about 5%. There is a need to clearly delineate the incidence of ONJ in osteoporosis patients treated with bisphosphonates, and in appropriate control populations. Based on current evidence, the risk of ONJ in osteoporosis appears to be comparable to that in the general population. It is likely that ONJ results from direct toxicity to cells of bone and soft tissue from high potency bisphosphonates, probably acting through their effects on the mevalonate pathway. The bone in ONJ lesions does not appear to be 'frozen', rather there is very active resorption present, probably stimulated by local infection. This is likely to result in the local release at high concentrations of bisphosphonates. Management focuses on prevention, treatment of infection and cessation of bisphosphonates. The role of surgery is unclear.
机译:现在,颌骨坏死(ONJ)的定义是口腔中存在裸露的骨头,经过六到八周的适当干预后,骨头无法愈合。在唑来膦酸盐,帕米膦酸盐或这些药物的组合治疗的患者中,通常是通过拔牙而沉淀出来的,用于治疗骨髓瘤,乳腺癌或前列腺癌。用双膦酸盐治疗的这些恶性肿瘤患者的总患病率约为5%。有必要明确描述在用双膦酸盐治疗的骨质疏松症患者中以及在适当的对照人群中ONJ的发生率。根据目前的证据,骨质疏松症中ONJ的风险似乎与普通人群相当。 ONJ可能是由高效双膦酸盐对骨骼和软组织细胞的直接毒性所致,可能是通过它们对甲羟戊酸途径的作用而起作用的。 ONJ病变中的骨骼似乎没有“冻结”,而是存在非常活跃的吸收作用,可能是受到局部感染的刺激。这很可能导致高浓度的双膦酸酯局部释放。管理重点是预防,治疗感染和停止双膦酸盐治疗。手术的作用尚不清楚。

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