FORTY YEARS FOLLOWING PAEDIATRIC CHONDROMYXOID FIBROMA OF THE DISTAL FEMUR: A CASE REPORT AND REVIEW OF THE LITERATURE
DOI:
https://doi.org/10.48188/hczz.6.1.9Keywords:
CHONDROMYXOID FIBROMA, FIBROMA, BENIGN NEOPLASMS, RECURRENCE, RESIDUAL NEOPLASM, MAGNETIC RESONANCE IMAGING, POSITRON EMISSION TOMOGRAPHY, COMPUTED TOMOGRAPHY, LONG-TERM FOLLOW UP, CASE REPORTAbstract
Background: Chondromyxoid fibroma (CMF) is a rare type of benign bone tumour comprising less than 2% of all benign bone neoplasms; it predominantly affects young individuals and typically arises in the metaphysis of long bones. Despite its benign nature, CMF poses diagnostic and therapeutic challenges due to its potential for local recurrence and its radiological resemblance to chondrosarcoma.
Case Presentation: We report the case of a 9-year-old girl diagnosed with CMF of the distal femur in 1985. She underwent curettage twice, three years apart, with histological confirmation of CMF. Following surgical management, the patient remained asymptomatic and functionally unrestricted for nearly four decades. At the age of 49, she presented with medial knee pain, unrelated
to tumour recurrence. Imaging studies, using magnetic resonance imaging and computed tomography (MRI and CT), revealed multiple small, well-defined lesions in the left femoral diaphysis, radiologically consistent with residual CMF. The lesions were asymptomatic and biologically inactive. A multidisciplinary evaluation supported conservative management and follow-up imaging.
Discussion: This case highlights the importance of long-term monitoring in patients with CMF and raises the question of
whether late-appearing lesions represent true recurrence or, more likely in this case, post-surgical residuals with no biological activity. Positron emission tomography and computed tomography (PET/CT) may offer additional insights into the metabolic activity of such lesions, aiding in differentiation and treatment planning. Our case underscores the relevance of a tailored, patient-centred
approach that leverages modern imaging and minimally invasive diagnostics.
Conclusion: CMF requires careful long-term follow-up, due to the potential for recurrence and rare malignant transformation. This case demonstrates that residual lesions may persist without clinical consequences for decades and that advanced imaging techniques play a crucial role in ongoing evaluation and management.
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