Panicker NK, Archana C Buch, Kunal Garg and Vijay H Satav
A case of ossifying fibromyxoid tumour of the soft part, a rare neoplasm arising about the knee of a young man is reported. The tumour has the characteristic morphology, having a thin bony shell, vascular myxohyaline stroma with oval or slightly spindly epitheloid cells arranged in cord pattern. The important histomorphological features have been highlighted and illustrated. The histogenesis, biological behavioral variations and differential diagnosis has been briefly discussed.
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