1. UNUSUAL MORPHOLOGIC PRESENTATION OF AN AMELOBLASTIC FIBROMA IN A YOUNG PATIENT
- Author
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Pedro José Targino Ribeiro, Tiago João Da Silva Filho, Jozinete Vieira Pereira, Daliana Queiroga de Castro Gomes, Igor Figueiredo Pereira, Waleska Ohana de Souza-Melo, and Ernani Canuto Figueirêdo Júnior
- Subjects
Pathology ,medicine.medical_specialty ,business.industry ,Odontogenic tumor ,Multilocular Lesion ,Ghost cell ,medicine.disease ,Pathology and Forensic Medicine ,Malignant transformation ,Lesion ,Calcifying odontogenic cyst ,Ameloblastic fibroma ,medicine ,Radiology, Nuclear Medicine and imaging ,Dentistry (miscellaneous) ,Surgery ,Oral Surgery ,medicine.symptom ,business ,Dental papilla - Abstract
Ameloblastic fibroma (AF) is a rare mixed odontogenic tumor that may present with aggressive behavior and may have potential for malignant transformation. Despite its very well-established histopathologic patterns, AF may have different types of tissues that might affect the final diagnosis, treatment choices, and outcome. An 11-year-old female patient presented with a well-defined multilocular lesion related to the impacted left inferior second molar, which was submitted to incisional biopsy. At the microscopic analysis, mesenchymal (resembling dental papilla) and epithelial (resembling odontogenic epithelium and disposed in small nests and cords) proliferating components were observed, characterizing as AF. Moreover, cystic degenerations, clear cells, ameloblastoma-like nests, and an epithelial fragment with ghost cells resembling the calcifying odontogenic cyst lining were found. The patient underwent another incisional biopsy, but no additional unusual features were found. Thus, treatment was decided as the total removal of the lesion and long-term follow-up.
- Published
- 2020
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