Iwase Masayasu, Fukuoka Airi, Tanaka Yoko, Saida Naoyuki, Onaka Eriko, Bando Sanae, Kondo Gen
Department of Dentistry and Oral Surgery, Hakujikai Memorial General Hospital, Tokyo, Japan.
Department of Oral and Maxillofacial Surgery, School of Dental Medicine, Tsurumi University, Kanagawa, Japan.
Case Rep Pathol. 2017;2017:7031414. doi: 10.1155/2017/7031414. Epub 2017 May 11.
Desmoplastic ameloblastoma (DA) is one of the 6 histopathological subtypes of ameloblastoma. Hybrid lesions in which histopathologically conventional ameloblastoma coexists with areas of DA are rare. A 40-year-old male was referred to our hospital complaining of a swelling in the right premolar region of the mandible. A panoramic radiograph showed an area of radiolucency with a well-defined corticated border, whereas computed tomography revealed a unilocular radiolucent lesion and buccal expansion together with cortical perforation. The lesion was treated via enucleation and curettage of the marginal bone and fenestration. A histopathological examination showed a hybrid ameloblastoma with a pronounced desmoplastic pattern and follicular changes. The patient's postoperative course has been favorable up to now, and no marked changes have been observed. We presented a case of hybrid ameloblastoma and reviewed the 36 reported cases of hybrid ameloblastoma that have been reported in the English literature.
促结缔组织增生性成釉细胞瘤(DA)是成釉细胞瘤6种组织病理学亚型之一。组织病理学上传统成釉细胞瘤与促结缔组织增生性成釉细胞瘤区域共存的混合性病变较为罕见。一名40岁男性因下颌右前磨牙区肿胀前来我院就诊。全景X线片显示一透光影区域,边界清晰有骨皮质包绕,而计算机断层扫描显示一单房性透光影病变,伴有颊侧膨隆及皮质穿孔。该病变通过摘除、刮除边缘骨及开窗术进行治疗。组织病理学检查显示为混合性成釉细胞瘤,具有明显的促结缔组织增生模式及滤泡样改变。患者术后恢复良好,至今未观察到明显变化。我们报告了一例混合性成釉细胞瘤病例,并回顾了英文文献中报道的36例混合性成釉细胞瘤病例。