From the department of Oral Pathology, Maulana Azad Institute of Dental Sciences.
*Aadithya B Urs, Senior Professor and Head of department of Oral Pathology.
J Clin Pediatr Dent. 2022 Mar 1;46(2):148-151. doi: 10.17796/1053-4625-46.2.10.
We report a rare case of dentinogenic ghost cell tumor (DGCT) associated with complex composite odontoma in a 17 years male affecting the posterior segment of the mandible. On radiographic examination, there was a well-defined multilocular radiolucency surrounding the radio opaque mass with respect to 44, 45 and 46. Histopathologically it showed ameloblastomatous proliferation with dentin like areas and ghost cells. It was associated with tooth like structures consisting of dentin, cementum and pulp like areas. DGCT with odontoma is extremely rare with only two cases being reported in literature till date. The management with its rare occurrence is discussed here.
我们报告了 1 例罕见的下颌后段牙源性影细胞肿瘤(DGCT)伴复合型牙源性混合瘤,涉及 17 岁男性。影像学检查显示,44、45 和 46 周围有一个界限清楚的多房性透亮区,围绕着一个不透射线的肿块。组织病理学表现为有牙本质样区和影细胞的釉细胞瘤样增生。它与牙样结构有关,包括牙本质、牙骨质和牙髓样区域。DGCT 伴牙源性混合瘤极为罕见,文献中仅有两例报道。本文讨论了其罕见的发病情况及治疗方法。