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PubMed · 6256934

Myofibroblasts in soft tissue sarcomas.

R Lagacé·W Schürch·T A Seemayer
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Abstract

A series of 129 soft tissue sarcomas was examined ultrastructurally to determine in which neoplasms and to what extent myofibroblasts could be demonstrated. Twenty cases of fibromatosis and fasciitis served as controls. Myofibroblasts were identified in all 30 cases of malignant fibrous histiocytoma and all 4 cases of well-differentiated sclerosing liposarcoma. Though most numerous in areas of desmoplasia, in no instance did myofibroblasts constitute the dominant cellular constituent of either neoplasm. Myofibroblasts were identified with lesser frequency and in smaller numbers in fibrosarcoma, synovial sarcoma, malignant hemangiopericytoma and neuroblastoma. None were observed in a wide assortment of diverse sarcomas in which desmoplasia was not a feature. In comparison each lesion judged by light microscopy to represent either fibromatosis or fasciitis was composed principally of myofibroblasts. The demonstration of abundant myofibroblasts within a soft tissue lesion which has been subjected to wide sampling strongly suggests a benign proliferative process as opposed to a malignant neoplasm. It is hypothesized that myofibroblasts observed within collagenized regions of soft tissue sarcomas may constitute an expression of host response to neoplasia.

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FibroblastsFibrosarcomaHemangiopericytomaHistiocytoma, Benign FibrousHumansLiposarcomaMicroscopy, ElectronNeuroblastomaSarcomaSarcoma, SynovialSoft Tissue NeoplasmsJournal Article

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BibTeXRIS

R Lagacé, W Schürch, T A Seemayer. 1980. Myofibroblasts in soft tissue sarcomas.. https://doi.org/10.1007/bf00428664

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