| Autor: |
Farhane, Fatima Zahra, Alami, Zineb, Bouhafa, Touria, Elmazghi, Abderrahmane, Hassouni, Khalid |
| Předmět: |
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| Zdroj: |
Pan African Medical Journal; 2015, Vol. 21, p1-6, 6p |
| Abstrakt: |
The extraskeletal myxoid chondrosarcoma (CME) is a rare malignant soft tissue tumour described as a distinct clinical, histological, immunohistochemical, genetical and evolutive entity. It represents only 2.5% of soft tissue sarcomas. Its individualization is important because it has a long and indolent clinical course, and tumour-related death often occurs after a long survival period. The diagnostic key is morphological supported by immunohistochemistry and genetics t (9; 22) that allow differentiating it from other tumours with myxoid stroma and from chordoma. This report describes a patient with paravertebral extraskeletal myxoid chondrosrcoma with a high locoregional extension. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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