成釉细胞瘤钙化囊性牙源性肿瘤:罕见的组织学变异

F. M. Abbas, M. Moshref, S. Sargolzaei, N. Kargahi
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引用次数: 4

摘要

根据2005年世界卫生组织(WHO)的新分类,钙化性牙源性囊肿(COC)或钙化性囊性牙源性肿瘤(CCOT)是一种罕见的发育性牙源性病变,具有组织病理学多样性。它主要发生在口腔前部,在生命的第二和第三个十年。牙源性肿瘤如成釉细胞瘤已被报道与CCOT相关。在本文中,我们报告一例成釉细胞瘤的CCOT在一个男孩与下颌支受累-一个极其罕见的组织学变异。镜检显示CCOT;结缔组织壁成釉岛内可见鬼影细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AMELOBLASTOMATOUS CALCIFYING CYSTIC ODONTOGENIC TUMOR: A RARE HISTOLOGIC VARIANT
In agreement with the new classification of the World Health Organization (WHO) 2005, calcifying odontogenic cyst (COC) or calcifying cystic odont-ogenic tumor (CCOT) is an uncommon developmental odontogenic lesion that demonstrates histopathologic diversity.  Predominantly, it occurs in the anterior region of the mouth and in the second and third decades of life. Odontogenic tumors such as ameloblastoma have been reported to be associated with CCOT. In this paper, we report a case of ameloblastomatous CCOT in a boy with involvement of mandibular ramus- an extremely rare histologic variant. The microscopic examination revealed a CCOT; ghost cell within ameloblastic islands in the connective tissue wall was observed.
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