Very rare intraoral appearance of ossifying fibro myxoid tumor: A case report
Ossifying fibro myxoid tumor (OFMT) is a rare soft tissue neoplasm and may present diagnostic difficulty. Only a few cases of oral cavity are described. A 49 –year-old male presented with a mass in the vestibular region of the mandible middle line, complaining of pain for the last three months. The...
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2020-12-01
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doaj-6685390936ca4d93860d561ec0f5747e2020-12-19T05:07:31ZengElsevierOral and Maxillofacial Surgery Cases2214-54192020-12-0164100196Very rare intraoral appearance of ossifying fibro myxoid tumor: A case reportÜmit Ertas0Ömer Gunhan1Yunus Emre AŞÇI2Atatürk University Faculty of Dentistry Head of Oral and Maxillofacial Surgery Department, Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Ataturk University, 25240, Erzurum, TurkeyDepartment of Pathology, TOBB ETU School of Medicine, Ankara, TurkeyDepartment of Oral and Maxillofacial Surgery, Faculty of Dentistry, Ataturk University, 25240, Erzurum, Turkey; Corresponding author. Tel./Fax: 90 442 231 2734.Ossifying fibro myxoid tumor (OFMT) is a rare soft tissue neoplasm and may present diagnostic difficulty. Only a few cases of oral cavity are described. A 49 –year-old male presented with a mass in the vestibular region of the mandible middle line, complaining of pain for the last three months. The mass contains spindle and polygonal mesenchymal cells on the myxoid ground in histochemical examinations. The tumor had a partial fibrous capsule surrounded by a non-metaplastic bone trabeculae. Histopathological examination was typical for OFMT. Although most cases of OFMT follow a benign course, recurrence and metastasis have been reported. Therefore, this type of tumor should be followed carefully.http://www.sciencedirect.com/science/article/pii/S2214541920300572Ossifying fibro myxoid tumorMezenchymal neoplasmSubcutaneous |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ümit Ertas Ömer Gunhan Yunus Emre AŞÇI |
spellingShingle |
Ümit Ertas Ömer Gunhan Yunus Emre AŞÇI Very rare intraoral appearance of ossifying fibro myxoid tumor: A case report Oral and Maxillofacial Surgery Cases Ossifying fibro myxoid tumor Mezenchymal neoplasm Subcutaneous |
author_facet |
Ümit Ertas Ömer Gunhan Yunus Emre AŞÇI |
author_sort |
Ümit Ertas |
title |
Very rare intraoral appearance of ossifying fibro myxoid tumor: A case report |
title_short |
Very rare intraoral appearance of ossifying fibro myxoid tumor: A case report |
title_full |
Very rare intraoral appearance of ossifying fibro myxoid tumor: A case report |
title_fullStr |
Very rare intraoral appearance of ossifying fibro myxoid tumor: A case report |
title_full_unstemmed |
Very rare intraoral appearance of ossifying fibro myxoid tumor: A case report |
title_sort |
very rare intraoral appearance of ossifying fibro myxoid tumor: a case report |
publisher |
Elsevier |
series |
Oral and Maxillofacial Surgery Cases |
issn |
2214-5419 |
publishDate |
2020-12-01 |
description |
Ossifying fibro myxoid tumor (OFMT) is a rare soft tissue neoplasm and may present diagnostic difficulty. Only a few cases of oral cavity are described. A 49 –year-old male presented with a mass in the vestibular region of the mandible middle line, complaining of pain for the last three months. The mass contains spindle and polygonal mesenchymal cells on the myxoid ground in histochemical examinations. The tumor had a partial fibrous capsule surrounded by a non-metaplastic bone trabeculae. Histopathological examination was typical for OFMT. Although most cases of OFMT follow a benign course, recurrence and metastasis have been reported. Therefore, this type of tumor should be followed carefully. |
topic |
Ossifying fibro myxoid tumor Mezenchymal neoplasm Subcutaneous |
url |
http://www.sciencedirect.com/science/article/pii/S2214541920300572 |
work_keys_str_mv |
AT umitertas veryrareintraoralappearanceofossifyingfibromyxoidtumoracasereport AT omergunhan veryrareintraoralappearanceofossifyingfibromyxoidtumoracasereport AT yunusemreasci veryrareintraoralappearanceofossifyingfibromyxoidtumoracasereport |
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