Giant Cell Tumor (GCT)
Overview
GCBT is an aggressive benign bone tumour, classified as intermediate (locally aggressive) in the 2020 WHO classification.
Accounts for 5–10% of all primary bone tumours.
Typically affects individuals aged 20–40 years.
Female > Male (1.3–2:1).
Associated conditions: Noonan syndrome, Paget’s disease.
Common Sites
Most common: Knee region (distal femur, proximal tibia)
Also seen in: Distal radius, proximal humerus, sacrum (most common axial site)
Clinical Presentation
Persistent pain (most common)
Joint swelling, limited motion, or pathological fracture (5–10%)
Palpable mass (if soft tissue extension exists)
No constitutional symptoms
Imaging Features
X-ray:
Eccentric, lytic lesion
No sclerotic rim, no calcification
Cortical expansion without periosteal reaction
Wide transition zone in fibula/ulna
Aggressive signs: Geographic destruction, soft tissue mass, fluid-fluid levels (if secondary ABC)
CT:
Detects lung metastases, evaluates axial involvement and trabecular pattern
MRI:
T1: Hypo- to isointense
T2: Hyperintense, heterogeneous
Shows soft tissue extension and blooming on GRE (hemosiderin)
Campanacci Classification
Used as a surgical guide.
Differential Diagnosis
Chondroblastoma: Epiphyseal, sclerotic rim, surrounding bone marrow oedema
Aneurysmal Bone Cyst (ABC): May co-exist, lacks soft tissue mass
Brown Tumour: Consider if high PTH
Treatment
Surgical Management (Extremities)
Intralesional curettage + adjuvant (phenol, ethanol, cryotherapy, argon gas, high-speed burr) + PMMA or graft
PMMA advantages: Exothermic necrosis, easier recurrence detection
Risks: Subchondral damage → early osteoarthritisWide resection: Indicated in Campanacci 3, distal ulna/proximal fibula
Denosumab (pre-op): Used to shrink tumour for limb-salvage surgery in Campanacci 3
Management of Pelvic & Axial GCBTs
Surgery carries high local complication risk
Grade 1–2: Intralesional resection after radioembolization
Grade 3:
If feasible → Wide resection ± radioembolization
If unresectable → Denosumab aloneRadiotherapy: Only for inoperable cases (malignant transformation risk)
Medical Therapy
Denosumab (RANKL inhibitor):
Pre-op or in inoperable patients
Avoid in Grade 1–2: Can reduce curettage efficacy and increase recurrence
Risks: Malignant transformation with long-term use, osteonecrosis of jaw
Bisphosphonates (e.g., zoledronic acid):
Reduces tumour size
Side effects: ONJ, atypical femur fracture, oesophagitis, hypo-/hypercalcemia
Metastasis & Complications
Lung metastases: Typically indolent; metastasectomy for progressive disease
Recurrence: 20–50% within 3 years, higher in axial/distal radius sites
Malignant transformation: Rare but severe (e.g., UPS or osteosarcoma, linked to denosumab)
PMMA-induced osteoarthritis due to chondral necrosis
References
Siegel, G. W., & Biermann, J. S. Orthopaedic Knowledge Update®: Musculoskeletal Tumors 5
Kang, H. S., et al. Oncologic Imaging: Bone Tumors, Springer
Choi, J. H., & Ro, J. Y. 2020 WHO Classification of Bone Tumors
Bayram, S., et al. EFORT Open Rev, 2024;9(3):181–189
