Fink Nadia Rahman, Pedersen Freddy Karup, Gyhrs Annette V Falkenberg
BørneUngeKlinikken, Rigshospitalet, Blegdamsvej 9, 2100 København Ø.
Ugeskr Laeger. 2014 May 19;176(21).
X-linked hypophosphataemia (XLH) is the most common form of hereditary rickets. We present a case report of a girl who was diagnosed with XLH. She was treated with activated vitamin D and phosphate and received several correctives surgical procedures. After a knee surgery, complicated with osteomyelitis, she presented with symptoms of severe calciphylaxis with calcification of several organ systems. Medical therapy was paused and systemic inflammation was treated with steroids and loop diuretics. This case report underlines the necessity of careful dosage of vitamin D and pausing of medical therapy after surgical procedures in patients with XLH.
X连锁低磷血症(XLH)是遗传性佝偻病最常见的形式。我们报告一例被诊断为XLH的女孩病例。她接受了活性维生素D和磷酸盐治疗,并接受了多次矫正手术。一次膝关节手术后,并发骨髓炎,她出现了严重钙质沉着的症状,多个器官系统出现钙化。暂停了药物治疗,使用类固醇和袢利尿剂治疗全身炎症。本病例报告强调了XLH患者手术过程后谨慎使用维生素D剂量以及暂停药物治疗的必要性。