Ossifying fibromyxoid tumor: A rare case report with review of literature and its differential diagnosis
| Autor: | Karthik Dhandapani, Jahnavi Gandhi, Amisha Gami |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2024 |
| Předmět: | |
| Zdroj: | Indian Journal of Pathology and Microbiology, Vol 67, Iss 3, Pp 672-676 (2024) |
| Druh dokumentu: | article |
| ISSN: | 0377-4929 0974-5130 |
| DOI: | 10.4103/ijpm.ijpm_298_22 |
| Popis: | Ossifying fibromyxoid tumor (OFMT) is a rare mesenchymal tumor of uncertain histogenesis with intermediate malignant potential presenting commonly in the fifth to sixth decade in the proximal limb and limb girdle. A 65-year-old male patient presented with a slow-growing gluteal mass. Wide local excision performed showed a well-defined tumor in the subcutaneous plane with a partially hard outer shell. Microscopy showed a moderately cellular tumor having cords and nests of round to ovoid cells with moderate cytoplasm and bland nuclei embedded in a myxo-hyaline matrix. An incomplete peripheral rim of ossification was seen. Pleomorphism/high cellularity was not seen. Mitosis was |
| Databáze: | Directory of Open Access Journals |
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