
Learn the Excision of osteochondroma from the medial distal femur surgical technique with step by step instructions on OrthOracle. Our e-learning platform contains high resolution images and a certified CME of the Excision of osteochondroma from the medial distal femur surgical procedure.
Osteochondromas represent approximately 1/3 of all benign bone tumours. They are an exostosis of bone that is covered by cartilage on its external surface. They typically present in the second or third decades of life and most frequently effect the appendicular skeleton, with the lower limbs more commonly effected. They may be solitary or multiple hereditary osteochondromatosis. The risk of sarcomatous change is rare, seen in approximately 1% of solitary osteochondromas, with rates of 1-25% seen in multiple hereditary osteochrondromatosis.
Surgery for benign osteochondromas should be avoided and only performed if they cause pain, decreased range of motion, pressure on neurovascular structures, tendon irritation or significant bursal formation.
In this case a young male patient had pain and limitation of deep flexion, which was interfering with his active job. Previously he had suffered a fracture of the stalk of the osteochondroma. A period of conservative management had been tried prior to offering excision. An MRI pre-operatively confirmed there was no suggestion of malignant transformation.

INDICATIONS
Indications for surgical removal include pain per se, or due to symptomatic compression of local anatomy such as nerve, blood vessels or tendons.
SYMPTOMS & EXAMINATION
Classically a discreet, well defined bony mass is noted in the lower or upper limbs. They may well be asymptomatic. If present symptoms will include pain, decreased range of motion, pressure on neurovascular structures, tendon irritation or significant bursal formation. A sudden change in symptoms should prompt re-evaluation and may indicate malignant transformation to a chondrosarcoma.
Such secondary chondrosarcomas arise in the cartilage cap of a longstanding osteochondroma. Those located in the pelvis and scapula seem to be the most susceptible to malignant change, perhaps because these sites permit undetected growth. Malignant transformation occurs in 1% of solitary osteochondromas and in 4% of patients with multiple osteochondromas (diaphyseal aclasia). This change is often seen in the fourth decade. MO is an autosomal dominant disorder; in almost 90% of MO patients germline mutations in the tumour suppressor genes EXT1 or EXT2 are present.
IMAGING
Xray findings are very characteristic and allow quantification and documentation of size and location.
MRI imaging is used exclude malignant transformation or assist in diagnosis if plain X-Rays are equivocal. A cartilage cap thicker than 1.5 cm when measured with MRI may indicate malignant change and surgical excision


Full weight bear
Histology from specimen
Remove bandages 24 hours
Wound check 2 weeks
Analgesia
Physiotherapy as needed
Avoid heavy manual work and impact sports for 3 months.

Surgical treatment of symptomatic osteochondroma. JBJS Br 2003;85B:1161-5.
Bottner et al.
The majority of patients had osteochondroma’s removed for pain. Local recurrence was noted more frequent in cases of mulitple hereditary osteochondroma’s occurring in 3 of 30 verses 1 of 56 solitary osteochondromas excised. Almost 85% of patients were satisfied with the outcome of surgery
A very comprehensive review of the condition is available open access on the journal RadioGraphics, 2000.
Imaging of osteochondroma: Varients and complications with radio-pathologic correlation.
Mark D Murphey et al
https://pubs.rsna.org/doi/full/10.1148/radiographics.20.5.g00se171407
Another very useful open access paper is to be found in the journal Human Mutation from 2009.
Multiple Osteochondromas: Mutation Update and Description of the Multiple Osteochondromas Mutation Database (MOdb)
Ivy Jennes et al.
https://onlinelibrary.wiley.com/doi/epdf/10.1002/humu.21123
Reference
- orthoracle.com

































