Kim S, Park C H, Chung Y S
Department of Nuclear Medicine, Ajou University School of Medicine, Suwon, Korea.
Clin Nucl Med. 2000 May;25(5):337-40. doi: 10.1097/00003072-200005000-00003.
Hypophosphatemic osteomalacia, a familial or rarely acquired disorder, is characterized biochemically by hypophosphatemia, decreased renal tubular reabsorption of phosphate, decreased intestinal absorption of calcium, and normal serum calcium. This report concerns a rare case of hypophosphatemic osteomalacia of unknown cause that was shown on Tc-99m MDP bone scanning.
低磷性骨软化症是一种家族性或罕见的后天性疾病,其生化特征为低磷血症、肾小管对磷的重吸收减少、肠道对钙的吸收减少以及血清钙正常。本报告涉及一例病因不明的低磷性骨软化症罕见病例,该病例在Tc-99m MDP骨扫描中显示。