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Undifferentiated Pleomorphic Sarcoma (UPS) (Malignant Fibrous Histiocytoma (MFH) and Myxofibrosarcoma)

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Management of Soft Tissue Sarcoma

Abstract

The most common term for a generic high-grade sarcoma has evolved over the years from fibrosarcoma to malignant fibrous histiocytoma (MFH), and now to high-grade undifferentiated pleomorphic sarcoma (UPS), as of the writing of the 2013 WHO sarcoma fascicle. The new nomenclature is utilized to differentiate from tumors that are truly histiocytic, i.e., histiocytic sarcoma, recognizing that their microscopic morphology is not specific for this sarcoma subtype. Specific varieties of what was called MFH in the past have proved to be unique entities. For example, myxofibrosarcoma is now a clearly defined sarcoma subtype that was formerly termed myxoid MFH. Myxofibrosarcoma occurs more frequently in the subcutaneous tissue and has infiltrating pattern (Fig. 7.1). Angiomatoid MFH is reclassified as angiomatoid fibrous histiocytoma, having mostly a benign clinical course and occurring in children and young adults. The situation is further complicated since the term MFH is still sometimes employed as a term for a high-grade bone sarcoma that lacks osteoblastic or chondroblastic differentiation (and treated most commonly as osteogenic sarcoma in children). Increasingly, the term UPS of bone is increasingly used instead of MFH of bone.

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Brennan, M.F., Antonescu, C.R., Alektiar, K.M., Maki, R.G. (2016). Undifferentiated Pleomorphic Sarcoma (UPS) (Malignant Fibrous Histiocytoma (MFH) and Myxofibrosarcoma). In: Management of Soft Tissue Sarcoma. Springer, Cham. https://doi.org/10.1007/978-3-319-41906-0_7

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  • DOI: https://doi.org/10.1007/978-3-319-41906-0_7

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