| Literature DB >> 36002688 |
Makihito Hamamoto1, Hiroaki Shimamoto2, Kaori Oya3, Yasuo Fukuda3, Sven Kreiborg1,4,5,6,7, Sanjay M Mallya1,8, Fan-Pei Gloria Yang1,9,10, Shumei Murakami1.
Abstract
An ameloblastic fibroma with formation of dental hard tissues, which the classical name is ameloblastic fibro-odontoma (AFO), is a rare type of mixed odontogenic tumor. An 8-year-old boy was diagnosed with AFO, with an inhomogeneous high signal within the lesion shown by T2-weighted magnetic resonance imaging (MRI). Computed tomography (CT) imaging revealed a unilocular low CT value area of 24 × 19 × 26 mm with buccolingual bony expansion and cortical bone thinning on the left side of the mandible including the crown of the mandibular left second molar. In addition, multiple calcified bodies were detected within the lesion, one of which had a CT value of approximately 2200 HU, equivalent to that of enamel. MRI indicated the lesion to be sized 24 × 19 × 25 mm along with buccolingual bony expansion in the left side of the mandible. Additionally, the lesion showed an internal inhomogeneous high signal, while a portion had an especially high signal in T2-weighted images. That particularly high signal area coincided with the nodular growth area of mucus-rich mesenchymal components without the epithelial component in histopathology findings. The particularly high signal revealed by T2-weighted imaging could be attributed to the mucus-rich component. MRI was found useful for revealing differences in the internal histopathological properties of an AFO in our patient.Entities:
Keywords: Ameloblastic fibro-odontoma; Ameloblastic fibroma; Benign tumor; Hamartoma; MRI
Year: 2022 PMID: 36002688 DOI: 10.1007/s11282-022-00649-4
Source DB: PubMed Journal: Oral Radiol ISSN: 0911-6028 Impact factor: 1.882