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Indian J Surg Oncol. 2018 Jun;9(2):260-264. doi: 10.1007/s13193-018-0759-1. Epub 2018 Apr 21.

Juvenile Trabecular Ossifying Fibroma-a Case Report.

Author information

1
1Oral Health Research Center, Institute of Health, Babol University of Medical Sciences, Babol, Iran.
2
2Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Babol University of Medical Sciences, Babol, Iran.
3
Department of Oral and Maxillofacial Pathology, Bandarabbas University of Medical Sciences, Bandar Abbas, Iran.
4
4Department of Oral and Maxillofacial Pathology, Faculty of Dentistry, Babol University of Medical sciences, Babol, Iran.
5
5Department of Oral and Maxillofacial Surgery Specialized, Babol University of Medical Sciences, Babol, Iran.

Abstract

Ossifying fibroma is a benign osteogenic mesenchymal tumor that is classified in the fibro-osseous lesions. Fibro-osseous lesions contain minerals, blood vessels, and giant cells that have the same radiographic and pathologic features but have different clinical behaviors, and were replaced with the normal bone. These lesions include fibrous dysplasia, cemento-osseous dysplasia, and ossifying fibroma. Juvenile ossifying fibroma is a type of uncommon and has invasive behavior, high incidence and occurs in young men, especially in maxilla, and is different from the type of adult in age, location, and clinical behavior and microscopic view. Pathologically, ossifying fibroma is divided into two types of trabecular and psammomatoid. The trabecular type is characterized by the presence of the osteoid trabeculae and the woven bone, and the type of psammomatoid by the presence of round, integrated, and small ossicles that are similar to the components of the psammoma. The purpose of this report is the clinical examination, radiography, pathology, and the treatment of a rare case of ossifying fibroma (trabecular) in mandible in a 7-year-old boy.

KEYWORDS:

Fibro-osseous lesions; Mandible; Ossifying fibroma; Trabecular

PMID:
29887713
PMCID:
PMC5984869
[Available on 2019-06-01]
DOI:
10.1007/s13193-018-0759-1

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