成釉细胞瘤样钙化囊性牙源性肿瘤累及下颌前部区域：一例罕见病例报告。
Ameloblastomatous calcifying cystic odontogenic tumour involving the mandibular anterior region: An unusual case report.
作者信息
Gade Lalitkumar P, Jagtap Kiran S, Lunawat Snehal D, Choudhary Sneha H
机构信息
Department of Oral Pathology, SMBT Dental College and Hospital and Post Graduate Research Center, Sangamner, Maharashtra, India.
Department of Oral Pathology, SMBT Institute of Dental Sciences and Research Center, Dhamangaon, Nashik, Maharashtra, India.
出版信息
J Oral Maxillofac Pathol. 2023 Jan-Mar;27(1):216-219. doi: 10.4103/jomfp.jomfp_419_20. Epub 2023 Mar 21.
Ameloblastomatous calcifying odontogenic cyst (COC) is a very rare histopathological variant of COC, which is an odontogenic cyst of the jaw. The term "calcifying odontogenic cyst" is not covered in the World Health Organisation (WHO) Classification of Tumors 2005 and was re-named as calcifying cystic odontogenic tumour (CCOT). There are only a few reports containing details on CCOT being associated with ameloblastoma. This variant has been classified as ameloblastomatous CCOT (type 3) as per the WHO 2005 classification. In this article, we reported an exceptional case of ameloblastomatous CCOT in a 15-year-old boy involving the mandibular anterior region, which is a rare combination for age and site of the lesion, along with an impacted tooth which is again an uncommon association.
成釉细胞瘤样钙化牙源性囊肿（COC）是牙源性囊肿——牙源性钙化囊肿（COC）一种非常罕见的组织病理学变体。“钙化牙源性囊肿”这一术语未被世界卫生组织（WHO）2005年肿瘤分类涵盖，并被重新命名为钙化囊性牙源性肿瘤（CCOT）。仅有少数报告详细介绍了与成釉细胞瘤相关的CCOT。根据WHO 2005年分类，这种变体已被归类为成釉细胞瘤样CCOT（3型）。在本文中，我们报告了一例15岁男孩下颌前部区域的成釉细胞瘤样CCOT罕见病例，该病例在病变的年龄和部位方面都很罕见，同时还伴有一颗阻生牙，这也是一种不常见的关联情况。
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