Ludwig Boltzmann Institute of Osteology at the Hanusch Hospital of WGKK and AUVA Trauma Centre Meidling, 1st Med. Dept., Hanusch Hospital, Vienna, Austria.
Institute of Radiology and Nuclear Medicine, Hanusch Hospital, Vienna, Austria.
J Bone Miner Res. 2018 Mar;33(3):534-539. doi: 10.1002/jbmr.3319. Epub 2017 Nov 21.
Intravenous infusions of different iron formulations are recognized as a cause of hypophosphatemia. Chronic hypophosphatemia can alter bone metabolism and bone material structure. As a consequence, osteomalacia may develop and lead to bone fragility. Herein, we report a patient with Crohn's disease presenting with persistent hypophosphatemia and insufficiency fractures while receiving regular iron infusions due to chronic gastrointestinal bleeding. Previously, the patient regularly received vitamin D and also zoledronic acid. The patient underwent bone biopsy of the iliac crest that showed typical signs of osteomalacia with dramatically increased osteoid volume and decreased bone formation. Analysis of the bone mineralization density distribution (BMDD) revealed a more complex picture: On the one hand, there was a shift to higher matrix mineralization, presumably owing to low bone turnover; on the other hand, a broadening of the BMDD indicating more heterogeneous mineralization due to osteomalacia was also evident. This is the first report on changes of bone histomorphometry and bone matrix mineralization in iron-induced osteomalacia. © 2017 American Society for Bone and Mineral Research.
静脉输注不同的铁制剂已被确认为低磷血症的原因。慢性低磷血症可改变骨代谢和骨物质结构。因此,可能会发展为佝偻病,并导致骨骼脆弱。在此,我们报告一例克罗恩病患者,因慢性胃肠道出血而经常接受铁输注,出现持续性低磷血症和骨脆性骨折。此前,患者定期接受维生素 D 和唑来膦酸治疗。患者行髂嵴骨活检,显示典型的佝偻病表现,类骨质体积显著增加,骨形成减少。骨矿化密度分布(BMDD)分析显示出更为复杂的情况:一方面,由于骨转换率低,基质矿化向更高值转移;另一方面,由于佝偻病导致矿化更不均匀,BMDD 也变宽。这是第一篇关于铁诱导性佝偻病中骨组织形态计量学和骨基质矿化变化的报告。 © 2017 美国骨矿研究学会。