[Keratocystic odontogenic tumor: a case report].

K H Moukram, S Haitami, I Ben Yahya
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引用次数: 0

Abstract

First described by Philipsen in 1956, the odontogenic keratocyst is characterized by a large squamous keratinization of its border, an aggressive growth and a high recurrent rate. It is now designated by the World Health Organization as a Keratocystic Odontogenic Tumor (KOT). Clinically, the KOT is manifested by an asymptomatic growth. Radiographically, it appears as a well-defined unilocular or multilocular osteolytic lesion. The diagnostic approach is based on a combined analysis of the medical history, the clinical appearance and the radiographic appearance. The diagnosis may be confirmed by the anatomical pathology report. Finally, treatment consists of surgical excision and follow up is characterized by a high rate of recurrence. The authors report a case of keratocystic odontogenic tumor of the mandible and review the various diagnoses, therapeutics and follow up aspects of this type of tumors.

角化囊性牙源性肿瘤1例。
由Philipsen于1956年首次描述,牙源性角化囊肿的特征是其边界有很大的鳞状角化,具有侵袭性生长和高复发率。它现在被世界卫生组织指定为角化囊性牙源性肿瘤(KOT)。临床上,KOT表现为无症状的生长。x线片表现为明确的单房或多房溶骨性病变。诊断方法是基于对病史、临床表现和影像学表现的综合分析。解剖病理报告可证实诊断。最后,治疗包括手术切除和随访,其特点是复发率高。本文报告1例下颌骨角化囊性牙源性肿瘤,并对该类型肿瘤的诊断、治疗及随访方面作一综述。
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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