Basal cell ameloblastoma: A rare variant with a comprehensive literature review

Nikita Kashyap , Sudipta Rakshit , S. Aravindan , S. Srihari
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引用次数: 0

Abstract

Ameloblastomas represent a diverse and mystifying group of odontogenic tumors. Basal cell ameloblastoma (BCA) is the rarest histological variant, characterized by densely packed nests and strands of primitive basaloid cells with inconspicuous stellate reticulum-like areas. Histopathologically, it closely resembles cutaneous basal cell carcinoma, basaloid squamous cell carcinoma and intraosseous adenoid cystic carcinoma posing a diagnostic challenge. Although primarily reported in peripheral locations, intraosseous occurrences are exceptionally rare, with only 30 cases documented in the literature to date. Here, we present a unique case of intraosseous basal cell ameloblastoma in a 60-year-old patient with a mandibular lesion. Given its rarity, this case contributes to the expanding knowledge of BCA and emphasize the importance of recognizing its distinct clinicopathological features for accurate diagnosis and management.
基底细胞成釉细胞瘤:一种罕见的变异,文献综述
成釉细胞瘤是一种多样而又令人费解的牙源性肿瘤。基底细胞成釉细胞瘤(Basal cell ameloblastoma, BCA)是最罕见的组织学变异,其特征是密集排列的巢和原始基底样细胞链,具有不明显的星状网状样区域。组织病理学上,它与皮肤基底细胞癌、基底样鳞状细胞癌和骨内腺样囊性癌非常相似,这给诊断带来了挑战。虽然主要报道外周部位,但骨内发生异常罕见,迄今文献中仅记录了30例。在这里,我们提出一个独特的病例骨内基底细胞成釉细胞瘤在一个60岁的病人与下颌骨病变。鉴于其罕见性,本病例有助于扩大对BCA的认识,并强调认识其独特的临床病理特征对准确诊断和治疗的重要性。
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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