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Extraskeletal myxoid chondrosarcoma: A clinicopathologic, immunohistochemical, and molecular analysis of 18 cases

✍ Scribed by Sumika Okamoto; Masanori Hisaoka; Tsuyoshi Ishida; Tetsuo Imamura; Hiroaki Kanda; Shyohei Shimajiri; Hiroshi Hashimoto

Book ID
117818491
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
652 KB
Volume
32
Category
Article
ISSN
1532-8392

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Extraskeletal myxoid chondrosarcoma : A
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## Abstract ## BACKGROUND Extraskeletal myxoid chondrosarcoma (EMC) is a rare malignant neoplasm. Despite a consensus for the distinct clinicopathologic entity of EMC, its clinical features remain controversial. In addition, most studies have contained a small number of patients who underwent defi

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Extraskeletal myxoid chondrosarcoma (EMC) is a rare soft tissue sarcoma that has been reported to have a relatively good prognosis. The authors report ten patients with EMC on whom there was a minimum follow-up of 10 years. The patients' ages ranged from 31 to 72 years (mean, 57 years); there were s

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Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma
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## Abstract Extraskeletal myxoid chondrosarcoma (EMC) is a soft‐tissue neoplasm cytogenetically characterized by the translocations t(9;22)(q22;q11–12) or t(9;17)(q22;q11), generating __EWS/CHN__ or __RBP56/CHN__ fusion genes, respectively. In the present study, 18 EMCs were studied both cytogeneti