A benign lesion derived from aberrant cartilage from the perichondral ring; the most common benign bone tumour
Aetiology
- Common in adolescents and young adults (10-20 years)
- Can be solitary or multiple
- Multiple osteochondromata can occur as an autosomal dominant hereditary disorder - Multiple Hereditary Exostosis (MHE)
Pathophysiology
- Produces a bony outgrowth on the external surface with a cartilaginous cap
Clinical presentation
- Commonly occur near the knee - distal femur/proximal tibia
- May be symptoms with activity - pain from tendons, numbness from nerve compression
Investigations
- Imaging (x-ray, MRI) - cartilage capped ossified pedicle
Management
- Close observation - small risk of malignant transformation (<1%) so any lesion growing in size or causing pain may require excision
- In MHE there are more tumours so higher change of malignancy