中央粒细胞牙源性肿瘤:病例报告及过去 71 年来所报告病例的文献综述。

Fatemeh Mashhadiabbas, Sanaz Gholami Toghchi, Roohollah Safarpour
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摘要

中央颗粒细胞牙源性肿瘤(CGCOT)是一种罕见、良性、生长缓慢的牙源性肿瘤。在2017年报告的世卫组织分类中,CGCOT未被视为一个独立的实体。本研究报告了一例罕见的CGCOT病例,患者为一名39岁的白人女性,累及右侧上颌前区。此外,为了更好地描述CGCOT的临床、影像学、组织病理学和免疫组化特征,本研究还对所有已发表的CGCOT病例(PubMed/ Google Scholar/ MEDLINE/Scopus)进行了文献综述。CGCOT 是一种非常罕见的肿瘤,文献中仅有 51 例报道。本病例的罕见之处在于它位于上颌前区,这在亚洲以前从未有过报道。本病例和文献综述中其他病例的免疫组化结果证实了颗粒细胞的间充质来源和上皮岛屿的牙源性性质,这为将来将该病变纳入世界卫生组织牙源性肿瘤分类提供了可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Central Granular Cell Odontogenic Tumor: Case Report with Literature Review of Cases Reported in the Last 71 years.

The central granular cell odontogenic tumor (CGCOT) is a rare, benign, slowly growing, odontogenic neoplasm. CGCOT was not considered as a distinct entity in the WHO classification reported on 2017. This study reports a rare case of CGCOT involving the right side of maxillary anterior region of a 39-year-old white woman. In addition, to better delineate the clinical, radiographic, histopathologic and immunohistochemical characteristics of CGCOT, a literature review of all published cases (in PubMed/ Google Scholar/ MEDLINE/Scopus) of CGCOT is provided. CGCOT is a very uncommon tumor, with only 51 reported cases in the literature. The present case is interesting regarding to its rarity for being in the maxillary anterior region, which has not been previously reported in Asia. The immunohistochemical findings of the current case and other cases in the literature review, verified the mesenchymal origin of granular cells and odontogenic nature of the epithelium islands, which can be a possible promise for placing this lesion in the future WHO odontogenic tumor classification.

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