Fibrosarcoma. The malignant tumor of fibroblasts

Stout, Arthur Purdy

doi:10.1002/1097-0142(194805)1:1<30::aid-cncr2820010104>3.0.co;2-d

Cited by 265 publications

(47 citation statements)

References 65 publications

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“…It is noteworthy that Stout in his classic 1948 paper on fibrosarcoma classified these tumors as congenital, fibroblastic, juvenile, myxoid, and pleomorphic variants [72,73]. Figure 9 of Hajdu's historic commentary on fibrosarcomas illustrates a ''high-grade pleomorphic fibro-sarcoma with pleomorphic fibroblasts in abundant collagenous matrix'' [73].…”

Section: A Proposed New Classification For Sarcomas Formerly Designatmentioning

confidence: 99%

The Rise and Fall of Malignant Fibrous Histiocytoma

Erlandson

Antonescu

2004

Ultrastructural Pathology

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Section: A Proposed New Classification For Sarcomas Formerly Designatmentioning

confidence: 99%

The Rise and Fall of Malignant Fibrous Histiocytoma

Erlandson

Antonescu

2004

Ultrastructural Pathology

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“…He defined fibrosarcoma as 'a tumor composed of spindle shaped fibroblasts and connective tissue fibers which are wrapped around all the cells rather than forming long wire.' 5 In the first, Armed Forces Institute of Pathology (AFIP) fascicle on soft tissue tumor (1953), the term 'nonmetastasizing fibrosarcoma' was placed under the heading of fibromatosis, while dermatofibrosarcoma under fibrosarcoma. However, these lesions were removed from these heading in their 2nd edition (1966).…”

Section: Discussionmentioning

confidence: 99%

Intraoral Soft Tissue Fibrosarcoma: A Case Report and Review

Tupkari¹,

Chettiakandy²,

Padawe³

et al. 2014

Journal of Contemporary Dentistry

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Adult fibrosarcoma (FS), defined by the World Health Organization as 'malignant neoplasm composed of fibroblasts with variable collagen production and, in classical cases, a 'herringbone' architecture', is a very rare soft tissue sarcoma. The earlier literature revealed that the adult fibrosarcoma was the most commonly occurring lesion, however the incidence of which has declined dramatically over the past several decades. This is due to evolution in the classification of soft tissue tumors, recognition of its subtypes and increased understanding of the many other mesenchymal and nonmesenchymal tumors. Sarcomas are the rare group of malignancies which accounts for less than 1% of all the body sarcomas of which 5 to 15% occurs in head and neck region. It involves deep soft tissues of extremities, trunk, head and neck. Among the head and neck region, intraoral adult fibrosarcomas are very rare without any sex predilection. A case of primary soft tissue FS in posterior mandible of an 13-year-old female patient is documented here, which will be an addition to the cases reported earlier in the literatures.

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“…Reexamination by x-ray on Sept. 2,1950, showed that the previously described nodule seen within the trachea, or main stem bronchus, was no longer demonstrable. Microscopic and Pathological Examination and Diagnosis.-Biopsy of the trachéal tumor was done.…”

mentioning

confidence: 85%