Oncogenic osteomalacia associated with mesenchymal tumor in the middle cranial fossa: A case report

被引:10
|
作者
Isao Chokyu
Kenichi Ishibashi
Takeo Goto
Kenji Ohata
机构
[1] Department of Neurosurgery, Osaka City University, Graduate School of Medicine, Abeno-ku, Osaka, 545-8585
关键词
Osteomalacia; Giant Cell Tumor; Hypophosphatemia; Middle Cranial Fossa; Serum Phosphate Level;
D O I
10.1186/1752-1947-6-181
中图分类号
学科分类号
摘要
Introduction. Tumor-induced osteomalacia is a paraneoplastic syndrome of hypophosphatemia. Osteomalacia causes multiple bone fractures and severe pain. Case presentation. We report the case of a 57-year-old Japanese man with tumor-induced osteomalacia associated with a middle cranial fossa bone tumor. The tumor was successfully resected by using a middle fossa epidural approach. His phosphate level recovered to a normal range immediately after the surgery. Conclusions: It is rare that tumor-induced osteomalacia originates from the middle skull base. This report suggests that, if patients have a clinical and biochemical picture suggestive of tumor-induced osteomalacia, it is crucial to perform a meticulous examination to detect the tumor or the lesion responsible for the tumor. The serum level of fibroblast growth factor 23 is the most reliable marker for evaluating the treatment outcome of tumor-induced osteomalacia. © 2012 Chokyu et al.; licensee BioMed Central Ltd.
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