Abstract
Fibrosarcoma can occur at all ages (Fig. 12.1) and in all sites (Fig. 12.2). Before the era of immunohistochemistry, fibrosarcoma was one of the most common diagnoses for a soft tissue sarcoma. With the development of immunohistochemical and molecular techniques, it is now rare for a sarcoma to be termed a fibrosarcoma, which by its name implies fibroblasts as the cell of origin. With increasing sophistication in diagnosis, more and more subtypes of fibroblastic sarcomas are now appreciated, all relatively rare tumors.
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Brennan, M.F., Antonescu, C.R., Maki, R.G. (2013). Fibrosarcoma and Its Variants. In: Management of Soft Tissue Sarcoma. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-5004-7_12
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DOI: https://doi.org/10.1007/978-1-4614-5004-7_12
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