Sala Alessandra, Mattano Leonard A, Barr Ronald D
Department of Pediatrics, McMaster University, HSC 3N27, 1200 Main Street West, Hamilton, Ont., Canada L8S 4J9.
Eur J Cancer. 2007 Mar;43(4):683-9. doi: 10.1016/j.ejca.2006.11.002. Epub 2006 Dec 13.
Osteonecrosis (ON) is recognised increasingly as a complication of the treatment of cancer in children and adolescents. It is especially prevalent among survivors of acute lymphoblastic leukaemia and non-Hodgkin lymphoma, in whom as many as 1/3 may be affected, likely reflecting the cumulative exposure to glucocorticosteroid therapy. The pathogenesis is complex and includes suppression of bone formation, expansion of the intra-medullary lipocyte compartment and a direct effect on nutrient arteries. Children > or =10 years of age are at particular risk and the disorder is substantially more common in Whites than in Blacks. Genetic predispositions have been identified. ON is often multi-articular and bilateral, affecting weight-bearing joints predominantly. Surgical management options are of concern in young growing subjects, although injection of autologous marrow into affected sites offers promising results. Other novel approaches include the use of anti-resorptive drugs and strategies for prevention, such as with lipid-lowering agents, are being explored.
骨坏死(ON)越来越被认为是儿童和青少年癌症治疗的一种并发症。它在急性淋巴细胞白血病和非霍奇金淋巴瘤幸存者中尤为普遍,其中多达三分之一的人可能会受到影响,这可能反映了糖皮质激素治疗的累积暴露。其发病机制复杂,包括抑制骨形成、骨髓脂肪细胞腔扩大以及对营养动脉的直接影响。10岁及以上的儿童尤其危险,这种疾病在白人中比在黑人中更常见。已经确定了遗传易感性。骨坏死通常是多关节和双侧的,主要影响负重关节。尽管将自体骨髓注射到受影响部位取得了有希望的结果,但手术管理方案在年轻生长的受试者中令人担忧。其他新方法包括使用抗吸收药物,并且正在探索预防策略,如使用降脂药物。