Ossifying Fibromyxoid Tumour of Soft Tissues: A Rare Case Report
Panicker NK, Archana C Buch*, Kunal Garg and Vijay H Satav
Department of Pathology, Padmashree Dr. D.Y.Patil Medical College, Pimpri, Pune, India
- *Corresponding Author:
- Archana Buch
Professor, B-603 Gold Coast
Ivory Estates, Someshwarwadi
E-mail: [email protected]
Received date: July 10, 2014; Accepted date: August 27, 2014; Published date: September 02, 2014
Citation: Panicker NK, Buch AC, Garg K, Satav VH (2014) Ossifying Fibromyxoid Tumour of Soft Tissues: A Rare Case Report. J Cancer Sci Ther 6:322-323. doi:10.4172/1948-5956.1000288
Copyright: © 2014 Panicker NK, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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.