Abstract
Definition: Malignant tumor composed of fibroblasts. It is a diagnosis of exclusion.
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Definition: Malignant tumor composed of fibroblasts. It is a diagnosis of exclusion.
Epidemiology: <1 % of adult soft tissues sarcomas. Medium age 45 years. No sex predilection.
Location: Most are deep tumors. Anywhere where fibrous tissue is found. Thigh, knee, trunk, arm, forearm. Rare in the head and neck. Hand and foot are most frequent sites of fibrosarcoma in the child.
Clinical: Palpable, globose, well-defined mass rarely >10 cm. It is slow growing (few weeks to 20 years). It is nearly or totally painless except when it compresses a nerve. In advanced forms it may adhere to the bone and ulcerate the skin.
Imaging: On X-rays: a mass denser than muscles. Calcifications are exceptional. Bone may be eroded or saucerized with minimal periosteal reaction. On CT: homogeneous density, compact soft tissue mass with ill-defined margins and poor enhancement after contrast administration. On MRI: inhomogeneous, lower or isointense signal as those of muscle on T1, 90 % marked, peripheral enhancement on gadolinium, and dark areas on a background of intermediate or high intensity on T2.
Histopathology: Low-grade well-differentiated tumor: firm, scar-like consistency, white yellow, rounded limits, growing in an expansile fashion with a pseudocapsule of reactive tissue that sharply delimits it from surrounding normal tissues. High-grade poorly differentiated tumor: soft, fish-flesh consistency, gray-white, irregular margins, growing in an invasive fashion without a capsule and with multiple processes that infiltrate the surrounding tissues, and satellites nodules isolated from the main tumor mass. On low-power view a uniform aspect of interlacing bundles of monomorphic spindle cells with interwoven parallel arranged eosinophilic collagen fibers. The cells are characteristically arranged in long, sweeping fascicles in a herringbone pattern. The cells have tapered darkly stained nuclei. High-grade lesions with marked anaplasia and pleomorphism are better classified as undifferentiated pleomorphic sarcoma. Immunohistochemistry is consistently positive for vimentin and may be positive for pan-muscle actin and smooth muscle actin.
Course and Staging: Fibrosarcoma can come from transformation of preexisting benign processes (neurofibromatosis, burn scars) and from radiation exposure. Any stage: more frequently stage IA and stage IIB. Low-grade and age <10 years are favorable prognostic factors. In children metastases are rare (<10 %). Lymph node metastases are rare (<5 %).
Treatment: Wide excision. In the adult and in a high-grade lesion, radical margins may be indicated. Radiotherapy is less effective, and it is used as adjuvant in high-grade tumors. Recent studies have demonstrated that adjuvant chemotherapy is useful for a better prognosis. When surgical margins are inadequate, local recurrence occurs in 50 % of cases. Lung metastases occur in 60 % of cases. Ten-year survival rate is 60 % for low-grade and 30 % for high-grade tumors.
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Selected Bibliography
Alaggio R, Bisogno G, Rosato A, Ninfo V, Coffin CM (2009) Undifferentiated sarcoma: does it exist? A clinicopathologic study of 7 pediatric cases and review of literature. Hum Pathol 40(11):1600–1610. Review
Bahrami A, Folpe AL (2010) Adult-type fibrosarcoma: A reevaluation of 163 putative cases diagnosed at a single institution over a 48-year period. Am J Surg Pathol 34(10):1504–1513
Collini P, Sorensen PH, Patel S, Blay JY, Issels RD, Maki RG, Eriksson M, del Muro XG (2009) Sarcomas with spindle cell morphology. Semin Oncol 36(4):324–337. Review
Fletcher CD, Dal Cin P, de Wever I, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, van den Berghe H, Vanni R, Willén H (1999) Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group. Am J Pathol 154(6):1841–1847
Wong SL (2008) Diagnosis and management of desmoid tumors and fibrosarcoma. J Surg Oncol 97(6):554–558. Review
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Gambarotti, M. (2014). Fibrosarcoma. In: Picci, P., Manfrini, M., Fabbri, N., Gambarotti, M., Vanel, D. (eds) Atlas of Musculoskeletal Tumors and Tumorlike Lesions. Springer, Cham. https://doi.org/10.1007/978-3-319-01748-8_65
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DOI: https://doi.org/10.1007/978-3-319-01748-8_65
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