Key result
An 11-year-old boy with metatarsal Ewing sarcoma successfully underwent a pedicled osteocutaneous fibular transfer after neo-adjuvant chemotherapy induced adamantinoma-like morphology.
Case Report (n=1)
Reports the first use of a pedicled osteocutaneous fibular transfer for a metatarsal malignancy and documents chemotherapy-induced squamous differentiation in Ewing sarcoma.
Should not yet change reconstructive practice in metatarsal tumors; hypothesis-generating for fibular transfer and chemotherapy-induced differentiation.
Adamantinoma-like Ewing sarcoma is a rare variant of Ewing sarcoma known to have histologic and immunohistochemical evidence of squamous differentiation. This variant most commonly occurs in the head and neck region with a few cases reported in long bones of the limbs. It may be associated with poorer clinical outcome and could pose a diagnostic challenge(s) particularly if it occurs in older patients or as a metastatic lesion. We present a case of Ewing sarcoma in the metatarsal of an 11 year old boy that manifested adamantinoma-like morphology after neo-adjuvant chemotherapy. Chemotherapy has been reported to induce neuronal maturation and rhabdoid morphology in cases of Ewing sarcoma, but no reports of treatment induced squamous differentiation with P40/P63 expression have been demonstrated. This is also the first documented case to use a pedicled osteocutaneous fibular transfer in a metatarsal malignancy, which is usually treated by either ray or below knee amputation.
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Marais et al. (2021) conducted a case report in Adamantinoma-like Ewing sarcoma (n=1). Pedicled osteocutaneous fibular transfer and neo-adjuvant chemotherapy was evaluated. An 11-year-old boy with metatarsal Ewing sarcoma successfully underwent a pedicled osteocutaneous fibular transfer after neo-adjuvant chemotherapy induced adamantinoma-like morphology.
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