25
Musculoskeletal Tumors
Eugene C. Lin and Abass Alavi
In a known bone or soft tissue lesion, positron emission tomography (PET) is of some value in determining whether the lesion is benign or malignant and in grading malignant lesions. In addition, bone or soft tissue lesions are detected incidentally on PET performed for other indications. The degree of fluorodeoxyglucose (FDG) uptake in the lesion can aid in differential diagnosis when correlated with conventional imaging modalities.
- Low uptake. A low level of uptake suggests that a bone lesion is likely benign (although there are false-negative results in plasma-cytoma and low-grade chondrosarcoma).
- High uptake. A high level of uptake is less specific. Although lesions with high uptake are more likely to represent malignancy (primary or metastatic), high uptake can be seen in a large number of benign lesions (see Pitfalls section).
- Chondrosarcoma versus enchondroma1
- Chondrosarcomas (Fig. 25.1) usually have less uptake than other sarcomas but more uptake than enchondromas.
- PET cannot distinguish between benign tumors and grade I chondrosarcomas.
- Grade II and III chondrosarcomas have higher glucose metabolism than low-grade cartilage tumors.
- A standardized uptake value (SUV) cutoff of 2.3 is helpful in differentiating grade II and III chondrosarcomas from low-grade tumors.
- Chondrosarcoma versus osteochondroma. Limited data suggest an SUV cutoff of 2.0 may differentiate benign from malignant osteochondromas.2
- PET. Sensitivity 93%, specificity 67%3
- These results were obtained using tumor-to-background ratio of 3.0 as a positive result.
- In general, malignant bone lesions have higher FDG uptake than benign lesions.
- Metastases have the highest uptake, usually more than primary malignant bone lesions.4
- However, benign bone tumors can have substantial FDG accumulation (> 2.0 SUV).
- Particularly true for histiocytic or giant cell-containing lesions (Fig. 25.2)
- False-negatives.3,5 Low-grade chondrosarcoma, plasmacytoma, myxoid tumors
- False-positives.6,7 Giant cell tumor, chon-droblastoma, fibrous dysplasia, sarcoidosis, Langer hans cell histiocytosis, nonossifying fibroma, osteoblastoma, aneurysmal bone cyst, Paget disease (active), enchondroma, chondromyxoid fibroma, desmoplastic fibroma, brown tumor, fibro-osseous defects, osteomyelitis, bone infarct, acute or sub-acute fracture
- Low uptake. Low FDG uptake is of limited value in differentiating benign from malignant soft tissue tumors, as it could be represent either a nonmalignant lesion or a low-grade sarcoma.
- High uptake. High uptake is more useful, as it usually indicates intermediate or high-grade malignancy. Although some benign lesions can have high uptake, radiographic correlation can often differentiate these lesions from sarcomas.
- Liposarcoma versus lipoma. Limited data suggest that an SUV cutoff of 0.81 may differentiate liposarcomas (Fig. 25.3) from lipomas.8
- PET. Sensitivity 92%, specificity 73%9
- These results were obtained using qualitative interpretation.
- Tumor grade. FDG uptake correlates with tumor grade.10
- Lesions with SUV ≥ 1.6 are usually high grade.
- Lesions with SUV < 1.6 are usually low grade or benign.
- Benign lesions. Benign soft tissue lesions usually do not have substantial FDG uptake.11
- Lipomas and hemangiomas have the lowest uptake.
- False-positives. High uptake can be seen in giant cell tumor of the tendon sheath, sarcoid, desmoid, and schwannomas. Uptake in a hibernoma can mimic a liposarcoma.12
- Delayed imaging. Delayed imaging can help differentiate benign from malignant tumors, as malignant lesions show an increase in uptake on delayed images.
PET is valuable in both osseous and soft tissue malignancies. The primary uses are staging, guiding biopsy, detecting recurrence, therapy response, and tumor grading.
The primary applications of PET are in guiding biopsy, therapy monitoring, and diagnosing local recurrence.
- Staging. PET is of limited value in staging osteosarcoma (Fig. 25.4).
- PET is less sensitive than bone scan for the detection of bone metastases from osteosarcoma.16