Gou Manting, Ma Zhongshu
Department of Endocrinology, Tianjin Medical University General Hospital, China.
J Int Med Res. 2018 Aug;46(8):3487-3490. doi: 10.1177/0300060518763708. Epub 2018 Apr 3.
We herein report two cases of Fanconi syndrome with refractory hypophosphatemic osteomalacia that was difficult to correct by phosphorus replacement therapy. The pathological result was a bony giant cell tumor and osteosarcoma, respectively. Interestingly, after resection of the tumors, the patient with osteosarcoma recovered completely but the patient with the bony giant cell tumor had a relapse. Although she underwent nine operations, her symptoms and laboratory tests did not improve. These findings indicate that Fanconi syndrome can result from a bone tumor.
我们在此报告两例范科尼综合征合并难治性低磷性骨软化症的病例,此类骨软化症难以通过补充磷疗法纠正。病理结果分别为骨巨细胞瘤和骨肉瘤。有趣的是,肿瘤切除后,骨肉瘤患者完全康复,但骨巨细胞瘤患者复发。尽管她接受了九次手术,其症状和实验室检查结果并未改善。这些发现表明范科尼综合征可能由骨肿瘤引起。