Multiple odontogenic keratocyst: A case report and review of literature

S. Ahuja, U. Ahuja, Nidhi Puri Narang
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引用次数: 1

Abstract

Odontogenic keratocysts (OKCs) may occur in two different forms, either as solitary (non syndromic OKCs) or as multiple OKCs (syndromic OKCs). Multiple OKCs are usually associated with Gorlin–Goltz syndrome with features like skin carcinomas and bifid ribs, eye, and neurologic abnormalities. We report a rare case of Gorlin–Goltz syndrome in a 35-year-old male patient who presented with a swelling in lower left back teeth region since 1 week. Apart from these, other findings observed in the patient were frontal bossing, depressed nasal bridge, ocular hypertelorism, prominent supra orbital ridge, and mild mandibular prognathism. On the basis of clinical and radiological evaluation, Enucleation was planned in all the three quadrants and histopathological evaluation revealed multiple OKC’s. Patient was followed-up multiple times for the duration of six months. This case report highlights the important findings and presentation of a rare case of Gorlin Goltz syndrome along with its review of literature. Keywords: Odontogenic keratocyst, Basal cell carcinoma, Bifid ribs, Gorlin Goltz Syndrome.
多发牙源性角化囊肿1例报告及文献复习
牙源性角化囊肿(OKCs)可能以两种不同的形式发生,要么是孤立的(非综合征性角化囊肿),要么是多发性角化囊肿(综合征性角化囊肿)。多发性OKCs通常与Gorlin-Goltzsyndrome相关,其特征包括皮肤癌、肋裂、眼和神经系统异常。我们报告罕见的病例Gorlin-Goltz综合征在一个35岁的男性患者谁提出了一个肿胀在左下后牙区域自1周。除此之外,患者的其他表现还包括额凸、鼻梁凹陷、眼远视、眶上脊突出和轻度下颌前突。在临床和影像学评估的基础上,三个象限均计划去核,组织病理学评估显示多发OKC。对患者进行了6个月的多次随访。本病例报告强调了一个罕见的Gorlin - Goltz综合征的重要发现和表现,并对其文献进行了回顾。关键词:牙源性角化囊肿,基底细胞癌,肋裂,Gorlin - Goltz综合征
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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