Related Experiment Video
Updated: May 19, 2026

07:00
Intra-iliac Artery Injection for Efficient and Selective Modeling of Microscopic Bone Metastasis
Published on: September 26, 2016
Mild 18 F-PSMA-1007 Uptake in a Giant Bone Island
Zhengguang Xiao1, Ting Chen2, Aisheng Dong3
1Department of Radiology, Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai.
Clinical Nuclear Medicine
|May 18, 2026
Summary
Giant bone islands, rare sclerotic lesions larger than 2.0 cm, can be detected using 18F-PSMA-1007 PET/CT. This imaging technique revealed mild uptake in a 2.2 cm giant bone island, suggesting potential osteoblastic activity.
Area of Science:
- Radiology
- Nuclear Medicine
- Orthopedic Oncology
Background:
- Giant bone islands, defined as bone islands with a diameter greater than 2.0 cm, are uncommon findings.
- Bone islands are typically benign, asymptomatic, and radiographically characterized by well-defined sclerotic lesions.
Purpose of the Study:
- To describe the 18F-PSMA-1007 Positron Emission Tomography/Computed Tomography (PET/CT) findings in a patient with a giant bone island.
- To evaluate the potential role of 18F-PSMA-1007 uptake in characterizing giant bone islands and its association with osteoblastic activity.
Main Methods:
- A case report detailing the imaging findings in a patient with a giant bone island.
- Utilized 18F-PSMA-1007 PET/CT to visualize and assess the metabolic activity of the giant bone island.
- Standard Computed Tomography (CT) was used to determine the size and morphology of the lesion.
Main Results:
- The giant bone island was located in the left femoral head and measured 2.2 cm in maximum diameter on CT.
- The lesion appeared as a well-defined sclerotic lesion.
- Mild 18F-PSMA-1007 uptake was observed in the giant bone island on PET imaging.
Conclusions:
- 18F-PSMA-1007 PET/CT can visualize giant bone islands.
- Mild 18F-PSMA-1007 uptake in a giant bone island may indicate underlying osteoblastic activity.
- Further research is warranted to understand the implications of PSMA expression in benign bone lesions.

