This site is targeted at medical and radiology professionals, contains user contributed content, and material that may be confusing to a lay audience. Use of this site implies acceptance of our Terms of Use.


Chondroblastomas (Codman tumour) are rare benign cartilaginous neoplasms that characteristically arise in the epiphysis or apophysis of a long bone in young patients 1-2,7.  Despite being rare, they are one of the most frequently encoutered benign epiphyseal neoplasms in skeletally immature patients.


Chondroblastomas represent less than 1% of all primary bone tumours, occurring predominantly in young patients (<20 years of age) 7. There is a male predilection 7.

Clinical presentation

Clinical presentation is non-specific and may include joint pain, muscle wasting, tenderness, and swelling/local mass. 


Microscopically they are composed of chondroblasts (no surprise there), chondroid matrix, cartilage with occasional giant multi-nucleated cells (which may lead to the incorrect diagnosis of giant cell tumour).

Calcium deposition surrounding the chondroblasts, which are typically polyhedral shape, results in typical "chicken-wire calcification"  (pathognomonic) 7,10

Malignant transformation has been seen in a small proportion of cases, with local and vascular invasion, and distant metastases.

Aneurysmal bone cysts can be seen secondarily to underlying chondroblastoma.


Chondroblastomas most frequently arise in the epiphyses of long bones, with 70% occurring in the humerus (most frequent), femur and tibia9. ~10% are found in the hands and feet 7.  

Radiographic features

Chondroblastomas (along with chondromyxoid fibroma) constitute the “C” in the FEGNOMASHIC mnemonic for benign appearing cystic lesions 3.

Plain film

Chondroblastomas are seen as well defined lucent lesions, with either smooth or lobulated margins and a thin sclerotic rim, arising eccentrically in the epiphysis of long tubular bone such as the femur, humerus, or tibia or apophysis such as greater trochanter, greater tuberosity, calcaneus or talus. Internal calcifications can be seen in up to 40-60% of cases 7,9.  A joint effusion is seen in ~1/3 of patients. They range in size from 1-10 cm, with most being 3-4 cm at diagnosis 10.


CT demonstrates the plain film findings with better delineation of the relationship to the growth plate and articular surface. Solid periosteal reaction (seen in up to 50% of cases) and internal calcification (calcified matrix seen in ~1/2 of cases) and cortical breach are also more easily appreciated 7-8. Endosteal scalloping may be seen 10.


MRI is ideal for the evaluation of transphyseal or transcortical extension, and for demonstrating associated surrounding bone marrow and soft tissue oedema, which is seen in a large proportion of cases 5,7

These lesions have signal typical of cartilage:

  • T1:  lesion itself is of low to intermediate signal
  • T2/STIR: lesion is of intermediate to high signal

Fluid-fluid levels may occasionally be seen (see fluid fluid level containing bone lesions) presumably due to an associated aneurysmal bone cyst 4.

Treatment and prognosis

Treatment typically consists of curettage and packing of the resulting cavity with either bone or bone cement (polymethylmethacrylate). Radiofrequency ablation has also been used 7.

Unfortunately due to their proximity to the articlular surface and growth plate complete eradication is difficult. As a result recurrence rates are relatively high (8-20%), and injury to the growth plate may result in growth arrest and limb-length discrepancy 7.


Complications associated with chondroblastomas include pathologic fractures and rarely, malignant transformation and pulmonary metastasis 6.

Differential diagnosis

The differential is that of other lesions which have a predilection for the epiphysis or apophysis (see differential for an epiphyseal lesion). Specific lesions to be considered include 10

Presence of bone marrow oedema frequently seen surrounding chondroblastomas is helpful, as it is not a usual feature of chondromyxoid fibromas, giant cell tumours or enchondromas 7.

Related articles

Bone tumours

The differential diagnosis for bone tumours is dependant on the age of the patient, with a very different set of differentials for the paediatric patient.

Updating… Please wait.


Error Unable to process the form. Check for errors and try again.

Alert_accept Thank you for updating your details.