Extra-osseous chondrosarcoma. Report of five cases and review of the literature.

Wu, Kao; Collon, D J; Guise, Edwin R

doi:10.2106/00004623-198062020-00004

Cited by 39 publications

(7 citation statements)

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“…That tumours arising in soft tissue may very rarely resemble the more common chondrosarcoma of bone, be they well or poorly differentiated, is probable but not well substantiated. In fact at least some well differentiated lesions so diagnosed in the past (Stout & Verner 1953, Goldenberg, Cohen & Steinlauf 1967, Wu, Collon & Guise 1980 most probably represent examples of soft tissue chondroma, a tumour notorious for its cytological pleomorphism (Dahlin & Salvador 1974, Chung & Enzinger 1978, Humphreys et et al 1986).…”

Section: Introductionmentioning

confidence: 99%

Extraskeletal myxoid chondrosarcoma: a histochemical and immunohistochemical study

1986

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In reviewing a large series of soft tissue sarcomas, nine cases of extraskeletal myxoid chondrosarcoma have been retrieved. These tumours, which principally presented in middle-aged adults, have been examined histochemically to determine the heteroglycan content of their myxoid matrix and immunohistochemically for the presence of S-100 protein. The principal mucopolysaccharides identified were chondroitin-4 and 6-sulphate and keratan sulphate; each of the tumours was S-100 positive. The relevance of these findings to the histogenesis and differential diagnosis of these uncommon neoplasms is discussed.

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Section: Introductionmentioning

confidence: 99%

Extraskeletal myxoid chondrosarcoma: a histochemical and immunohistochemical study

1986

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“…20 The tumor in the authors' case manifested a locally aggressive nature with recurrence in a matter of three months. Fifteen patients showed metastasis from four months to 17 years after excision, with a mean of three years.…”

Section: Discussionmentioning

confidence: 77%

Extraskeletal Soft-Tissue Chondrosarcoma

Amir¹,

Amir²,

Mogle³

et al. 1985

Clinical Orthopaedics and Related Research

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“…Approximately 14%-25% of MSCs occur in extraskeletal sites [3,4]. Unlike conventional chondrosarcomas, ESMCs have a female preponderance and occur most frequently in the brain, meninges, and lower extremities [5]. There are two principal age groups in which ESMC occur: those that arise in the central nervous system characteristically occur in the 20-to 30-year age group; ESMCs that arise in soft tissues usually occur in patients older than 40 years of age [6].…”

Section: Discussionmentioning

confidence: 99%