Nuclear imaging of bone tumors: FDG-PET

Semin Musculoskelet Radiol. 2001 Jun;5(2):183-7. doi: 10.1055/s-2001-15678.

Abstract

Positron emission tomography (PET) has become a very useful adjunct to anatomic imaging techniques, because it can provide an in vivo method for quantifying functional metabolism in normal and diseased tissues. Clinical trials with [(18)F] 2-deoxy-2-fluoro-D-glucose (FDG), the most commonly used radiolabeled tracer for PET imaging, has demonstrated increased accumulation of FDG in cancer tissue. FDG-PET is now widely used for the detection, differentiation, grading, staging, and monitoring of various neoplasms. However, the significance of FDG-PET in such evaluations of primary bone tumors and tumor-like lesions has not been extensively elucidated. In this article, we present recent advances in FDG-PET studies for evaluating primary bone tumors and tumor-like lesions.

Publication types

  • Review

MeSH terms

  • Bone Neoplasms / diagnostic imaging*
  • Diagnosis, Differential
  • Fluorodeoxyglucose F18*
  • Humans
  • Radiopharmaceuticals*
  • Sarcoma / diagnostic imaging
  • Tomography, Emission-Computed*

Substances

  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18