Imaging Principles
Plain radiography remains the first-line and often diagnostic in most bone tumors, while CT provides detailed cortical and 3D anatomical evaluation. MRI offers superior soft-tissue and marrow contrast, essential for assessing intramedullary extension and surgical margins. PET/CT assist in detecting metastases and evaluating treatment response.
1. Introduction
Imaging plays a central role in the diagnosis, staging, and surgical planning of musculoskeletal (MSK) tumors.
Plain radiography, CT, MRI, nuclear medicine scans, and PET/CT remain the core modalities, often complemented by angiography and ultrasound for specific indications.
Selection of modality depends on tumor type, location, aggressiveness, and tissue composition
2. Plain Radiography (X-ray)
Serves as the first-line imaging tool and remains diagnostic in >80% of bone tumor cases
Reveals:
Tumor location within the bone (epiphyseal, metaphyseal, diaphyseal).
Cortical destruction or thickening, periosteal reactions (e.g., Codman triangle, sunburst pattern).
Matrix type — osteoid, chondroid, or fibrous.
Soft-tissue calcification patterns suggesting tumor type.
Limitation: early detection in pelvic and spinal lesions is poor due to overlapping structures.
3. Computed Tomography (CT)
Preferred modality for assessing extent of cortical destruction and 3D anatomy.
Helical CT with ≤1 mm slice thickness allows high-resolution multiplanar and 3D reconstructions
Contrast-enhanced CT delineates:
Relationship of tumor to vessels and neurovascular bundles.
Vascular invasion or distortion aiding surgical planning.
3D reconstruction helps estimate need for en bloc vessel resection or approach modification.
4. Magnetic Resonance Imaging (MRI)
Superior to CT for evaluating intramedullary spread and extraosseous soft-tissue extension
Advantages:
Multiplanar imaging (axial, sagittal, coronal).
Excellent contrast resolution for tumor–muscle–fat differentiation.
Contrast-enhanced MRI defines vascular involvement, cystic components, and nerve proximity.
MRI is essential for surgical margin planning and defining safe resection limits.
Characteristic tumor appearances:
Lipomas, liposarcomas, PVNS, hemangiomas, and fibromatoses show distinctive patterns.
Pitfalls: Hemorrhagic high-grade sarcomas may mimic hematomas — clinical follow-up is vital.
5. Bone Scintigraphy (Bone Scan)
Used to detect metastatic spread or multifocal disease
Bone tumors imaging
Three-phase bone scan reflects tumor biologic activity:
“Tumor blush” pattern — increased uptake during late flow phase in malignant lesions.
Also used to monitor chemotherapy response by comparing uptake pre- and post-treatment.
6. Angiography and Venography
Angiography:
Demonstrates arterial displacement, occlusion, or encasement by tumors
CT angiography is increasingly replacing conventional techniques.
Preoperative embolization reduces intraoperative bleeding in hypervascular metastases (e.g., renal carcinoma).
Venography:
Shows venous obstruction or compression by tumor mass.
Indirectly suggests neural invasion when adjacent vein occlusion is present.
7. Positron Emission Tomography / CT (PET/CT)
Functional imaging using FDG uptake proportional to tumor glucose metabolism
Applications:
Initial staging, monitoring therapy response, and recurrence detection.
PET-CT fusion combines functional and structural data — useful in detecting small metastatic lesions.
Standardized Uptake Value (SUV) quantifies uptake, helping to distinguish malignancy from infection or inflammation.
8. Ultrasonography (USG)
Recommended initial test for superficial soft-tissue masses (per ACR Appropriateness Criteria)
Benefits:
No radiation, real-time vascular evaluation, dynamic movement analysis, cost-effective.
Evaluates echogenicity, margins, vascularity, and cystic vs. solid composition.
Diagnostic accuracy: 77–93%, though specificity for malignancy is limited.
Pitfall: differentiation between lipoma and liposarcoma remains challenging.
Suspicious features (pain, rapid growth) → further MRI required.
9. MRI
Next-line imaging if diagnosis remains uncertain after USG or radiographs
Provides superior soft-tissue contrast and local staging.
Diagnostic parameters:
Size (>5 cm), deep location, heterogeneous T2 signal, ill-defined margins, perilesional edema.
Necrosis, bone or neurovascular invasion → suggest malignancy.
Post-contrast MRI enhances diagnostic accuracy:
Differentiates cystic vs. solid lesions.
Identifies necrotic areas and optimal biopsy sites.
Reported sensitivity and specificity for differentiating benign vs. malignant: 64–93% and 82–85%, respectively.
10. CT and PET/CT in Soft-Tissue Tumors
CT acts as a second-line modality when MRI is nondiagnostic or contraindicated (e.g., pacemaker, claustrophobia).
Contrast-enhanced CT evaluates bone involvement and surgical planning.
PET/CT:
Not routine for primary diagnosis but valuable for metastatic work-up and treatment response evaluation.
Studies suggest PET/CT may help differentiate benign and malignant tumors, but ACR discourages routine use.
Key Findings
Optimal MSK tumor imaging requires multimodal integration.
Radiography and MRI form the diagnostic backbone, with CT and PET/CT for staging and surgical planning.
Ultrasound remains useful for superficial masses, while angiography assists in vascular evaluation.
Advances in functional imaging (PET/MRI) and 3D reconstruction continue to enhance preoperative accuracy and individualized treatment planning.
References
1. Rajakulasingam R, Stediuk K, Teh JJ, et al. Current progress and future trends in imaging of bone tumours. Eur Radiol Exp. 2021;5(1):27.
2. Shu H, Ma Q, Li A, et al. Diagnostic performance of US and MRI in predicting malignancy of soft tissue masses: using a scoring system. Front Oncol. 2022;12:853232.
3. Gitto S, Ippolito D, Bandiera E, et al. CT and MRI radiomics of bone and soft-tissue sarcomas. Insights Imaging.2024;15(1):16.
Modality | Main Role | Advantages | Limitations |
X-ray | Initial screening | Identifies matrix, periosteal reaction | Poor soft-tissue detail |
CT | Cortical detail, 3D mapping | High resolution | Radiation exposure |
MRI | Soft-tissue and marrow evaluation | Multiplanar, no radiation | Costly, motion artifacts |
Bone Scan | Detects metastases | High sensitivity | Low specificity |
Angiography | Vascular mapping | Guides embolization | Invasive |
USG | Superficial mass evaluation | Real-time, no radiation | Operator-dependent |
PET/CT | Functional staging | Detects active disease | Limited initial utility |
Summary Table of Modalities
