Abstract
Schwannoma is a rare benign intraosseous neoplasm, originating in Schwann cells of the nerve fibers and usually in sensitive nerves. It constitutes less than 1% of primary benign bone neoplasms. Most cases occur in the mandible; the sacrum is also a preferred site. Schwannomas are generally asymptomatic. Radiographs show a lucent, usually well-defined, intramedullary lesion. The tumor is very well-delimited, composed of spindle cells with wavy nuclei, with a focal palisading arrangement. Immunohistochemistry shows positivity for S100 protein. Once a relationship to neurofibromatosis is excluded, prognosis is excellent. Marginal resection or curettage is curative.
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Kalil, R.K. (2020). Schwannoma of Bone. In: Santini-Araujo, E., Kalil, R.K., Bertoni, F., Park, YK. (eds) Tumors and Tumor-Like Lesions of Bone. Springer, Cham. https://doi.org/10.1007/978-3-030-28315-5_46
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DOI: https://doi.org/10.1007/978-3-030-28315-5_46
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