Revision 25 for 'Giant cell tumour of bone'
Giant cell tumour of bone
A giant cell tumour (GCT) of bone is a relatively common bone tumour, usually benign and typically found in the metaepiphysis of long bones.
Demographics and clinical presentation
GCTs are common comprising 18 - 23% of benign bone neoplasms and 4 - 9.5% of all primary bone neoplasms 1. They almost invariably (97 - 99%) occur when growth plate has closed an is therefore seen typically early adult hood with 80% of cases reported between the ages of 20 and 50, with a peak incidence between 20 and 30 1.
There is overall a mild female predilection, especially when located in the spine, however malignant transformation is far more common in men (M:F 3:1) 1.
Presentation is not specific, typically presents insidiously and relates to bone pain, soft tissue mass, compression of adjacent structures or acutely with a pathological fracture.
They typically occur as single lesions. Although any bone can be affected the most common sites are 1-2:
- around the knee : distal femur and proximal tibia : 50 - 65%
- distal radius : 10 - 12%
- sacrum : 4 - 9%
Multiple locations : ≈ 1 % (multiple lesions usually occur in association with Paget's disease)
Macroscopically, giant cell tumours are variable in appearance, depending on amount of haemorrhage, presence of co-existent ABC, and degree of fibrosis.
These tumours contain numerous thin walled vascular channels predisposing to areas of haemorrhage and presumably related to the relatively frequent co-existence of aneurysmal bone cysts (ABC) found in 14% of cases 1-2,4.
Microscopically GCT are characterised by prominent and diffuse osteoclastic giant cells and mononuclear cells ( round, oval, or polygonal and may resemble normal histiocytes). Frequent mitotic figures in the mononuclear cells may be seen, especially in pregnant women or those on the oral contraceptive pill (due to increased hormone levels) 1.
It is important to realise that features may be difficult to interpret histologically with a relatively wide histological differential diagnosis (e.g. giant cell reparative granuloma, brown tumour, osteoblastoma, chondroblastoma, non-ossifying fibroma, and even osteosarcoma with abundant giant cells)1 thus making radiology indispensable to the interpretation of these lesions.
Four radiographic features are characteristic when a GCT is located in a long bones:
- occurs only with closed growth plate
- abuts articular surface : 84 - 99% come within 1 cm of the articular surface 1
- well defined with non-sclerotic margin
- eccentric : if large this may be difficult to asses
Plain film and CT
General radiographic features include:
- narrow zone of transition: a broader zone of transition is seen in more aggressive GCTs
- no surrounding sclerosis : 80 - 85%
- overlying cortex is thinned, expanded or deficient
- periosteal reaction is only seen in 10 - 30% of cases
- soft tissue mass is not infrequent
- pathological fracture may be present
- not matrix calcification / mineralisation
- low to intermediate solid component
- low signal periphery
- solid component enhance, helping distinguish GCT with ABC from pure ABC 3-4
- some enhancement may also be seen in adjacent bone marrow
- heterogeneous intermediate to high signal T2 2,4 - this is variable 1
- low signal periphery
- if an ABC component present, then fluid fluid levels can be seen
- high signal in adjacent bone marrow thought to represent inflammatory oedema 4
Most GCT demonstrate increased uptake on delayed images, especially around the periphery, with central photopenic region (doughnut sign). Increased blood pool activity is also seen, and can be seen in adjacent bones due to generalised regional hyperaemia (contiguous bone activity).
If performed, usually in the setting of pre-operative embolisation, angiography usually demonstrates a hypervascular tumour (2/3 cases) with the rest being hypo or avascular.
Treatment and prognosis
Classically treatment is with curettage and packing with bone chips, or polymethylmethacrylate (PMMA). Local recurrence is from the periphery of the lesion and has historically occurred in up to 40 - 60% of cases. Newer intraoperative adjuncts such as thermal or chemical treatment of the resection margins have lowered the recurrence rate to 2.5 - 10%1. Wide local excision is associated with a lower recurrence rate, but has greater morbidity.
Approximately 5 - 10% of GCTs are malignant 1. Sarcomatous transformation is seen, especially in radiotherapy treated inoperable tumours.
- chondroblastoma : epiphyseal, usually in skeletally immature patients
- chondromyxoid fibroma : metaphyseal, with a well defined sclerotic margin, with a multiloculated bubbly appearance 3
- aneurysmal bone cyst (ABC) : younger age group, but may co-exist with GCT; fluid-fluid levels
- non-ossifying fibroma : usually younger age group 4
- brown tumour : in the setting of hyperparathyroidism
- enchondroma : only really a consideration in lesions of small bones of the hand and foot 3
- haemophiliac pseudotumour
- chondrosarcoma : typically older age group
- metastases and multiple myeloma
- intraosseous ganglion cysts