Leehey D J, Ing T S, Daugirdas J T
Am J Med. 1985 Apr;78(4):708-10. doi: 10.1016/0002-9343(85)90419-x.
A 20-year-old man presenting with osteomalacia was found to have the Fanconi syndrome, as evidenced by hypophosphatemia with hyperphosphaturia, glycosuria in the presence of normoglycemia, and generalized aminoaciduria. After removal of a non-ossifying fibroma of the left tibia, the renal tubular abnormalities promptly resolved with subsequent healing of the osteomalacia. A humoral factor released from the tumor may have caused the disorder in proximal renal tubular cell transport.
一名20岁患骨软化症的男性被发现患有范科尼综合征,表现为低磷血症伴高磷尿症、血糖正常时出现糖尿以及全身性氨基酸尿。切除左胫骨的非骨化性纤维瘤后,肾小管异常迅速消失,随后骨软化症治愈。肿瘤释放的一种体液因子可能导致了近端肾小管细胞转运紊乱。