Department of Oral Pathology and Oral Biology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa.
Oral Radiol. 2021 Jul;37(3):537-542. doi: 10.1007/s11282-020-00492-5. Epub 2020 Nov 27.
Ghost cell odontogenic carcinoma (GCOC) is a rare malignant neoplasm, representing 3% of all ghost cell lesions of the jaws. They can arise de novo or from a pre-existing calcifying odontogenic cyst (COC) or dentinogenic ghost cell tumour (DGCT). A systematic review of the literature reported only 12 cases of a GCOC arising from a pre-existing COC. This report highlights an additional case of a GCOC arising from a pre-existing COC after 3 years in an adolescent male. The patient initially presented with a painless swelling of the right mandibular corpus. Panoramic radiographic examination showed an expansive unilocular radiolucent lesion. After 3 years, the radiographic features appeared more aggressive with increased expansion and cortical perforation. A wide surgical resection was performed, whereby the lesion was diagnosed as a GCOC. Due to the rarity of these malignant neoplasms, limited information is available regarding their biological behaviour. One-year follow-up revealed no clinical signs of recurrence.
牙源性影细胞瘤(GCOC)是一种罕见的恶性肿瘤,占颌骨所有影细胞瘤病变的 3%。它们可以是新生物,也可以由已存在的钙化牙源性囊肿(COC)或牙源性影细胞肿瘤(DGCT)发展而来。文献的系统回顾仅报道了 12 例由已存在的 COC 发展而来的 GCOC。本报告强调了另 1 例青少年男性的 GCOC 由已存在的 COC 发展而来,时间为 3 年后。患者最初表现为右侧下颌体无痛性肿胀。全景片检查显示膨胀性单房透亮病变。3 年后,影像学特征表现出侵袭性增加,膨胀和皮质穿孔。行广泛的手术切除,诊断为 GCOC。由于这些恶性肿瘤非常罕见,关于其生物学行为的信息有限。1 年的随访没有发现复发的临床迹象。