Mainenti P, Oliveira G S, Valério J B, Daroda L S L, Daroda R F, Brandão G, Rosa L E B
Department of Oral and Maxillofacial Surgery, Hospital Nove de Julho-Instituto Oncológico de Juiz de Fora, Juiz de Fora (MG), Brazil.
Int J Oral Maxillofac Surg. 2009 Mar;38(3):289-92. doi: 10.1016/j.ijom.2008.11.025. Epub 2009 Jan 15.
This paper reports one case, of an ameloblastic fibro-odontosarcoma (AFOS) affecting the mandible, in a 12-year-old girl. This neoplasm is a rare odontogenic neoplasm. To the authors' knowledge this is the fifteenth case of AFOS reported in English. The patient's chief complaint was a swelling in the face for 6 months. An incisional biopsy was performed diagnosing the case as an ameloblastic fibroma. After radiography ameloblastic fibro-odontoma was diagnosed. Computed tomography was performed and a stereolithography model made to plan the surgical procedures. A hemimandibulectomy followed by a vascularized fibular flap was then proposed. The surgery was uneventful. Microscopic features diagnosed an AFOS. After 23 months of close follow-up there is no sign of recurrence or metastasis. Dental implants were recently placed in the fibular flap.
本文报告了一例发生在一名12岁女孩下颌骨的成釉细胞纤维牙肉瘤(AFOS)病例。这种肿瘤是一种罕见的牙源性肿瘤。据作者所知,这是英文报道的第15例AFOS病例。患者的主要诉求是面部肿胀6个月。进行了切开活检,诊断该病例为成釉细胞纤维瘤。经影像学检查后诊断为成釉细胞纤维牙瘤。进行了计算机断层扫描并制作了立体光刻模型以规划手术程序。随后建议进行半侧下颌骨切除术并采用带血管的腓骨瓣修复。手术过程顺利。显微镜检查特征诊断为AFOS。经过23个月的密切随访,没有复发或转移的迹象。最近在腓骨瓣中植入了牙种植体。