Jihed Sghaier, Slim Afef, Charfeddine Abir, Smida Abdelkader, Abdellatif Chokri, Selmi Jamil
Department of Oral Medicine and Oral Surgery, Faculty of Dental Medicine of Monastir, Monastir, Tunisia.
Ann Maxillofac Surg. 2024 Jan-Jun;14(1):116-119. doi: 10.4103/ams.ams_7_24. Epub 2024 May 24.
Ameloblastic fibro-odontoma (AFO) is a rare mixed odontogenic tumour with a preferential location in the posterior mandible and with a variety of radiological aspects. We report two clinical cases of AFO in two rare locations and with unusual radiological aspects.
The first patient is a 37-year-old female with an asymptomatic intraoral swelling located in the anterior mandibular. The second patient is a 16-year-old girl with a chief complaint of missing maxillary canine.
Both cases were diagnosed with AFO.
For the first patient, a biopsy was performed, and for the second one, the lesion was surgically excised.
The first patient is under regular surveillance and the other was followed up for one year without any evidence of recurrences.
TAKE-AWAY LESSONS: Despite many efforts, the nature, histology and therapy of these lesions remain very confusing.
成釉细胞纤维牙瘤(AFO)是一种罕见的混合性牙源性肿瘤,好发于下颌后部,具有多种放射学表现。我们报告两例AFO的临床病例,其发生于两个罕见部位且具有不寻常的放射学表现。
首例患者为一名37岁女性,下颌前部存在无症状的口腔内肿物。第二例患者是一名16岁女孩,主要诉求为上颌尖牙缺失。
两例均诊断为AFO。
首例患者进行了活检,第二例患者的病变进行了手术切除。
首例患者接受定期监测,另一例患者随访一年无复发迹象。
尽管进行了很多努力,但这些病变的性质、组织学和治疗仍然非常令人困惑。