Li Bin-Bin, Gao Yan
Department of Oral Pathology, Peking University School, Hospital of Stomatology, Beijing, China.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009 May;107(5):691-5. doi: 10.1016/j.tripleo.2009.01.008. Epub 2009 Mar 9.
Dentinogenic ghost cell tumor (DGCT), also referred to as odontogenic ghost cell tumor, is a rare tumor classified as a neoplastic variant of calcifying odontogenic cyst (COC). Ghost cell odontogenic carcinoma (GCOC) is the especially rare malignant counterpart of DGCT and COC. The case of a middle-aged male with a maxillary DGCT which transformed to GCOC after 5 recurrences during a 21-year period is presented. When the diagnosis of GCOC (first identified as malignant after 17-year recurrence) was made, the tumor cells showed more obvious atypia, necrosis, and numerous mitoses, and interestingly the ghost cell was hard to find and even disappeared. The significances in pathologic diagnosis and clinical treatment are discussed.
牙源性影细胞肿瘤(DGCT),也被称为牙源性影细胞瘤,是一种罕见的肿瘤,被归类为钙化牙源性囊肿(COC)的肿瘤性变体。影细胞牙源性癌(GCOC)是DGCT和COC极其罕见的恶性对应物。本文报告了一例中年男性上颌DGCT病例,该病例在21年期间复发5次后转变为GCOC。当诊断为GCOC(17年后复发首次被确定为恶性)时,肿瘤细胞显示出更明显的异型性、坏死和大量有丝分裂,有趣的是,影细胞很难找到甚至消失了。文中讨论了其在病理诊断和临床治疗中的意义。