Papilliferous keratoameloblastoma: a case report with review of the literature.

IF 2.7
A B Urs, J Augustine, P Kumar, S Mohanty, S Jha
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Abstract

Ameloblastoma is the most common benign odontogenic tumour of the jaw bones and it exhibits a wide range of histopathological patterns. Papilliferous keratoameloblastoma (PKA), a rare variant of ameloblastoma, is characterized by the presence of papilliferous proliferations of the odontogenic epithelium, along with surface keratinization and keratin accumulation that may occur within the stroma. This report presents a rare case of PKA in a 44-year-old male patient who presented due to a recurrent exophytic growth in the right posterior mandible. A panoramic radiograph showed a well-defined multilocular radiolucency extending from the right body of the mandible to the anterior two-thirds of the ramus of the mandible. Analysis of an incisional biopsy of the cauliflower-like growth revealed a plexiform ameloblastoma with extraosseous extension. The growth enlarged again during the next 3 months and the patient was then operated on. The patient underwent resection of the right posterior mandible involving the second molar and ramus up to the coronoid, followed by stabilization of the mandible with a titanium plate. The final diagnosis of PKA was made on the basis of the unique histopathological features. A review of the literature on cases of PKA is included.

乳头状角膜成釉细胞瘤1例并文献复习。
成釉细胞瘤是颌骨最常见的良性牙源性肿瘤,它表现出广泛的组织病理学模式。乳突状角质成釉细胞瘤(PKA)是一种罕见的成釉细胞瘤,其特征是牙源性上皮存在乳突状增生,并伴有表面角化和角蛋白积聚,可能发生在基质内。本文报告一例罕见的PKA病例,患者为44岁男性,其表现为右后下颌骨复发性外生性生长。全景x线片显示清晰的多室透光区,从下颌骨右体延伸至下颌骨前三分之二分支。菜花样生长的切口活检分析显示一个网状成釉细胞瘤,并向骨外延伸。在接下来的3个月里,生长再次扩大,然后患者进行了手术。患者接受切除右后下颌骨,包括第二磨牙和支直至冠状骨,随后用钛板稳定下颌骨。PKA的最终诊断是基于其独特的组织病理学特征。对PKA病例的文献综述包括在内。
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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