| Literature DB >> 24900011 |
Hyo Jung Seo1, Yun Jung Choi1, Hyun Jeong Kim1, Yong Hyu Jeong1, Arthur Cho1, Jae Hoon Lee1, Mijin Yun1, Jong Doo Lee1, Won Jun Kang1.
Abstract
Oncogenic osteomalacia is a rare paraneoplastic syndrome characterized by renal phosphate excretion, hypophosphatemia, and osteomalacia. This syndrome is often caused by tumors of mesenchymal origin. Patients with oncogenic osteomalacia have abnormal bone mineralization, resulting in a high frequency of fractures. Tumor resection is the treatment of choice, as it will often correct the metabolic imbalance. Although oncogenic osteomalacia is a potentially curable disease, diagnosis is difficult and often delayed because of the small size and sporadic location of the tumor. Bone scintigraphy and radiography best characterize osteomalacia; magnetic resonance imaging findings are nonspecific. Here, we report a case of oncogenic osteomalacia secondary to a phosphaturic mesenchymal tumor that was successfully detected by (18)F-fluorodeoxyglucose positron emission tomography/computed tomography ((18)F-FDG PET/CT). This case illustrates the advantages of (18)F-FDG PET/CT in detecting the occult mesenchymal tumor that causes oncogenic osteomalacia.Entities:
Keywords: 18F-fluorodeoxyglucose; Oncogenic osteomalacia; Positron emission tomography
Year: 2011 PMID: 24900011 PMCID: PMC4043009 DOI: 10.1007/s13139-011-0095-7
Source DB: PubMed Journal: Nucl Med Mol Imaging ISSN: 1869-3474