Luo Hai Yan, Gao Yan
Department of Oral Pathology, Peking University School and Hospital of Stomatology, Beijing, PR China.
Chin J Dent Res. 2013;16(1):71-4.
Ghost cell differentiation within an ameloblastic fibroma is extremely rare. The ghost cells found in an ameloblastic fibroma in previously reported cases were all associated with a typical calcifying odontogenic cyst. Here, we report a case of an ameloblastic fibroma with focal ghost cells and calcifications in some neoplastic epithelial islands, but without other histologic manifestations consistent with a calcifying odontogenic cyst. The patient was a 13-year-old Chinese boy who presented with a bony-hard swelling in the posterior mandibular region over a 6-month period. Radiographs showed a well-defined multilocular radiolucency associated with an unerupted tooth. The lesion was mostly cystic-solid and comprised of odontogenic epithelial strands, islands and myxoid ectomesenchymal component microscopically. Small groups of ghost cells and calcification were noted in the epithelial islands.
成釉细胞纤维瘤内的影细胞分化极为罕见。在先前报道的病例中,成釉细胞纤维瘤中发现的影细胞均与典型的钙化牙源性囊肿相关。在此,我们报告一例成釉细胞纤维瘤,在一些肿瘤性上皮岛中有局灶性影细胞和钙化,但无其他与钙化牙源性囊肿一致的组织学表现。患者为一名13岁的中国男孩,下颌后部区域出现骨硬肿胀6个月。X线片显示一个边界清晰的多房性透射区,与一颗未萌出的牙齿相关。病变主要为囊实性,镜下由牙源性上皮条索、岛状结构和黏液样外胚间叶成分组成。上皮岛中可见小群影细胞和钙化。