Niu Haoman, Liu Junyu, Chen Yu, Geng Ning
State Key Laboratory of Oral Disease, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan 610041, P.R. China.
Department of Oral Pathology, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan 610041, P.R. China.
Mol Clin Oncol. 2017 Dec;7(6):971-975. doi: 10.3892/mco.2017.1448. Epub 2017 Oct 12.
Ameloblastic fibro-odontosarcoma (AFOS) is an extremely rare subtype of odontogenic sarcoma, with no more than 19 cases reported in the English literature to date. AFOS is a biphasic neoplasm, with deposits of dentin and enamel matrix. We herein present a case of AFOS with active epithelial proliferation in a 31-year-old female patient. The patient was referred to the West China Hospital of Stomatology (Chengdu, China) due to a 6-month history of a swelling in the left mandible. Following clinical and radiological examination, the initial preoperative diagnosis was ameloblastoma, with local invasion and the possibility of malignant transformation. Left hemimandibular resection was subsequently performed. The postoperative histopathological diagnosis was AFOS, accompanied by active epithelial proliferation. Immunohistochemically, cytokeratin (CK)14 and CK19 were intensely positive in the epithelium, whereas the mesenchymal cells were strongly positive for vimentin. The Ki-67 labeling index was considerably higher in the mesenchymal component (mean, 40%) compared with that in the epithelial element (mean, 5-8%). Three months after the surgical procedure, the patient remained clinically and radiologically disease-free.
成釉细胞纤维牙肉瘤(AFOS)是牙源性肉瘤中一种极其罕见的亚型,迄今为止英文文献报道不超过19例。AFOS是一种双相性肿瘤,有牙本质和釉质基质沉积。我们在此报告一例31岁女性患者的AFOS,伴有活跃的上皮增殖。该患者因左下颌肿胀6个月就诊于四川大学华西口腔医院(中国成都)。经过临床和影像学检查,术前初步诊断为成釉细胞瘤,伴有局部侵袭及恶变可能。随后进行了左半下颌骨切除术。术后组织病理学诊断为AFOS,伴有活跃的上皮增殖。免疫组化显示,细胞角蛋白(CK)14和CK19在上皮中呈强阳性,而间充质细胞波形蛋白呈强阳性。与上皮成分(平均5 - 8%)相比,间充质成分的Ki-67标记指数相当高(平均40%)。手术3个月后,患者临床和影像学检查均无疾病迹象。