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首页> 外文期刊>International Journal of Dentistry >Mew Dimensional Staging of Bisphosphonate-Related Osteonecrosis of the Jaw Allowing a Guided Surgical Treatment Protocols Long-Term Follow-Up of 266 Lesions in Neoplastic and Osteoporotic Patients from the University of Bari
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Mew Dimensional Staging of Bisphosphonate-Related Osteonecrosis of the Jaw Allowing a Guided Surgical Treatment Protocols Long-Term Follow-Up of 266 Lesions in Neoplastic and Osteoporotic Patients from the University of Bari

机译:颌骨的双膦酸盐相关骨坏死的喵尺寸分期,可对来自巴里大学的肿瘤和骨质疏松患者的266个病灶进行长期随访

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Bisphosphonates (BPs) are synthetic drugs analogues of inorganic pyrophosphate that can be divided into two groups, nitrogen-containing and non-nitrogen-containing BPs, with different mechanisms of action on osteoclasts [1, 2]. These compounds were originally licensed for the management of skeletal complications of malignancy, including advanced breast cancer and multiple myeloma, but now they are also the drugs of choice in the management of other bone disorders including osteoporosis, cancer-induced hypercalcaemia, Paget's disease, osteogenesis imperfecta [3-5], primary and secondary hyperparathyroidism, and other conditions that feature bone fragility [1]. The most serious side effect of BPs therapy is the bisphosphonate-related osteonecrosis of jaw (BRONJ), firstly described in 2003 by Marx [6]. BPs decrease both bone reabsorption and formation, leading to increased bone fragility and fractures caused by inability to replace old bone by young bone and to repair Microtracks [7]. According to the most widely used definition, given by the American Association of Oral and Maxillofacial Surgeons (AAOMS) and modified by Colella et al., BRONJ is the presence of exposed or otherwise necrotic bone for at least 8 weeks in patients with exposure to BPs and no history of radiotherapy to the jaw [6, 8, 9]. BRONJ can occur in patients receiving
机译:双膦酸盐(BPs)是无机焦磷酸盐的合成药物类似物,可分为两组,含氮和不含氮的BP,对破骨细胞具有不同的作用机制[1、2]。这些化合物最初被许可用于治疗包括晚期乳腺癌和多发性骨髓瘤在内的恶性骨骼并发症,但是现在它们还是用于治疗其他骨疾病(包括骨质疏松症,癌症引起的高钙血症,Paget病,成骨)的药物。不完美[3-5],原发性和继发性甲状旁腺功能亢进以及其他以骨脆性为特征的疾病[1]。 BPs治疗最严重的副作用是双膦酸盐相关的颌骨坏死(BRONJ),最早在2003年由马克思描述[6]。 BPs减少了骨的重吸收和形成,导致骨脆性增加和骨折,这是由于无法用年轻的骨头替代旧的骨头以及无法修复Microtracks引起的[7]。根据最广泛使用的定义(由美国口腔颌面外科医师协会(AAOMS)给出并由Colella等人修改),BRONJ是暴露于BP的患者中存在暴露或其他坏死骨至少8周而且没有对颌骨放疗的历史[6,8,9]。接受治疗的患者可能发生BRONJ

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