Pathologic hepatic Tc-99m-MDP uptake in polyostotic fibrous dysplasia

Ersoy Kekilli1, Cengiz Yagmur, Akin Kuzucu

  • 1Department of Nuclear Medicine, Inonu University, Turgut Ozal Medical Center, Malatya, Turkey. ekekilli@inonu.edu.tr

Annals of Nuclear Medicine
|December 14, 2004
PubMed

Insights

This study reports a rare case of liver uptake of Tc-99m-MDP in polyostotic fibrous dysplasia. Pamidronate treatment resolved the hepatic uptake, suggesting a link to crystal deposition.

Area of Science:

  • Nuclear Medicine
  • Radiopharmaceuticals
  • Skeletal Dysplasias

Background:

  • Fibrous dysplasia of bone is a rare congenital disorder causing bone deformities.
  • Hepatic technetium-99m-methylene diphosphonate (Tc-99m-MDP) uptake is an uncommon finding in bone scans.

Observation:

  • A 25-year-old male with severe polyostotic fibrous dysplasia showed increased Tc-99m-MDP uptake in bones and liver.
  • The patient received monthly intravenous pamidronate for two months.

Findings:

  • Follow-up bone scintigraphy revealed resolution of hepatic Tc-99m-MDP uptake despite persistent bone involvement.
  • This suggests pamidronate treatment may improve or resolve abnormal hepatic accumulation.

Implications:

  • Pathologic hepatic Tc-99m-MDP uptake in fibrous dysplasia might be associated with calcium oxalate and phosphate crystal formation.
  • Pamidronate therapy may be effective in managing this rare scintigraphic finding.

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