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低剂量阿德福韦酯治疗引起的低磷血症性骨软化症:重点关注骨骼系统的表现及文献复习。

Hypophosphatemic osteomalacia induced by low-dose adefovir therapy: focus on manifestations in the skeletal system and literature review.

机构信息

Department of Rehabilitation Medicine, Keimyung University School of Medicine, Daegu, Korea.

出版信息

J Bone Miner Metab. 2013 Mar;31(2):240-6. doi: 10.1007/s00774-012-0384-y. Epub 2012 Sep 14.

Abstract

Osteomalacia is a metabolic bone disease that leads to softening of the bones and can be caused by hypophosphatemia. Large clinical studies of low-dose adefovir dipivoxil (adefovir) have found no evidence of renal tubular dysfunction leading to hypophosphatemia after 48 weeks of treatment. We report two cases of low-dose adefovir-induced hypophosphatemic osteomalacia that initially presented with diffuse musculoskeletal pain. The first patient was a 62-year-old man with a 2-year history of bone pain involving the dorsal mid-thorax, lower anterior chest wall, right sacroiliac joint area, and both knees. The patient had been receiving adefovir for 5 years before confirmation of hypophosphatemia and urinary phosphate wasting. Bone scintigraphy revealed multifocal lesions including multiple ribs, costochondral junctions, costovertebral junctions, sacrum, both posterior iliac bones, both proximal tibia, right calcaneus, and the left second metatarsophalangeal joint area, which were suggestive of metabolic bone disorder. Bone pain was significantly reduced within 3 months after supplementation with phosphate and calcitriol. The second patient was a 54-year-old male who presented with an 18-month history of severe bone pain of the right medial knee and low back. The patient had been taking adefovir for approximately 40 months before the development of bone pain. Laboratory data revealed hypophosphatemia and vitamin D deficiency. Bone scintigraphy showed increased uptake in bilateral ribs, sternum, both scapulae, both costovertebral junctions, both pelvic bones, medial cortex of the right proximal femur, right proximal tibia, and the left lateral tarsal bone. The symptoms improved by changing the antiviral agent from adefovir to entecavir. Because osteomalacia often presents with diffuse bone pain, non-specific radiologic findings and non-characteristic routine serum biochemical changes, the disease can be confused with various musculoskeletal diseases and a high index of suspicion is necessary for an early diagnosis in patients receiving adefovir therapy.

摘要

骨软化症是一种代谢性骨病,可导致骨骼变软,可由低磷血症引起。阿德福韦酯(adefovir)低剂量的大型临床研究发现,在治疗 48 周后,没有证据表明肾小管功能障碍导致低磷血症。我们报告了两例低剂量阿德福韦酯引起的低磷血症性骨软化症,最初表现为弥漫性肌肉骨骼疼痛。第一例患者为 62 岁男性,有 2 年的胸椎中段、前胸下部、右侧骶髂关节区和双膝骨痛史。在确认低磷血症和尿磷酸盐丢失之前,该患者已接受阿德福韦治疗 5 年。骨闪烁显像显示多发性病变,包括多个肋骨、肋软骨连接处、肋椎关节、骶骨、双侧髂骨后部、双侧胫骨近端、右侧跟骨和左侧第二跖趾关节区,提示代谢性骨病。补充磷酸盐和骨化三醇后 3 个月内,骨痛明显减轻。第二例患者为 54 岁男性,右侧内侧膝关节和腰部严重骨痛 18 个月。在出现骨痛之前,该患者大约已服用阿德福韦 40 个月。实验室数据显示低磷血症和维生素 D 缺乏。骨闪烁显像显示双侧肋骨、胸骨、双侧肩胛骨、双侧肋椎关节、双侧骨盆、右侧股骨近端内侧皮质、右侧胫骨近端和左侧外侧跗骨骨摄取增加。将抗病毒药物从阿德福韦酯改为恩替卡韦后,症状得到改善。由于骨软化症常表现为弥漫性骨痛、非特异性放射学表现和非特征性常规血清生化变化,因此该疾病可能与各种肌肉骨骼疾病混淆,在接受阿德福韦酯治疗的患者中,需要高度怀疑才能早期诊断。

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