Treatment of Enchondroma
For solitary, asymptomatic enchondromas in the long bones, observation with annual radiologic follow-up is the preferred initial approach, as malignant transformation is exceedingly rare and surgical intervention carries considerable complication rates. 1, 2
Initial Management Strategy
Asymptomatic Lesions
- Active surveillance is now recommended by some reference centers for non-progressive asymptomatic lesions, particularly in the long bones of the extremities 3
- Annual radiologic follow-up should be performed for asymptomatic enchondromas or atypical cartilaginous tumors in long bones, irrespective of tumor size 2
- Only 6% of conservatively treated enchondromas required surgery for medical indications during follow-up 2
- The complication rate of enchondroma curettage is considerable (23% in one series), making observation a safer option for asymptomatic lesions 1
Symptomatic Lesions Requiring Surgery
- Curettage with or without local adjuvant therapy (phenol, cement, cryotherapy) is the standard treatment for symptomatic enchondromas 3
- Surgical indications include: persistent pain, radiologic growth, pathologic fracture, or patient preference after thorough discussion 2
- Most patients (81%) achieve full range of motion after curettage and bone grafting 4
Location-Specific Treatment Approaches
Hand Enchondromas
- Curettage is the standard of care for symptomatic lesions 5
- Cancellous bone grafting (autologous or allograft) is typically performed after curettage 6, 4
- Patients presenting with pathologic fracture have higher rates of postoperative extension deficit (28% vs 15%) 4
- In the phalanges of hands and feet, malignancy is extremely rare 3
Long Bone Lesions
- Atypical cartilaginous tumors in long bones of the limbs can be managed by curettage with or without local adjuvant therapy 3
- Alternative approach: active surveillance with close radiological monitoring for non-progressive asymptomatic lesions 3
Important Clinical Caveats
Signs of Malignant Transformation
- Pain at the site of a cartilaginous lesion may indicate malignancy 3
- Serial radiographs showing slow increase in size should raise concern 3
- Cartilage "cap" measuring >2 cm or documented growth after skeletal maturity suggests sarcomatous transformation 3
- Contrast-enhanced MRI can reveal high-grade areas and guide biopsy location 3
High-Risk Populations
- Patients with Ollier disease (enchondromatosis) have approximately 30% risk of malignant transformation to chondrosarcoma 3
- Patients with Maffucci syndrome also carry increased malignancy risk 3
- These syndromic patients require closer surveillance and should be counseled appropriately 3
- Recurrence rates are higher in patients with Ollier disease (23%) and giant form lesions (43%) 4
Surgical Technique Considerations
- Curettage followed by cancellous bone grafting is the most common approach 1, 6
- Internal fixation may not be necessary in all cases 4
- Adjuvant therapy options include phenol, cement, and cryotherapy 3
- Wide excision with negative margins is reserved for larger lesions or those with intraarticular/pelvic localization 3
Recurrence and Complications
- Recurrence of solitary enchondromas is rare (approximately 10% with minimum 2-year follow-up) 4
- Malignant transformation of solitary enchondroma to chondrosarcoma is exceedingly rare 1
- Postoperative complications include joint stiffness and soft-tissue deformities 5
- Most patients return to full function after surgery 5