Abstract
1. A series of thirty-two cases of chondromyxoid fibroma is reported.
2. The clinical, radiographic and pathological features are described.
3. The rarity of the tumour and of malignant change is stressed.
4. Excision or block resection is preferred to curettage as a method of treatment, because of the liability to recurrence after curettage.
5. It is suggested that the designation "fibromyxoid chondroma" is more appropriate than the usual designation "chondromyxoid fibroma".
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