Characteristic and Management of Ameloblastoma In Oral And Maxillofacial Surgery At Hasan Sadikin General Hospital: Retrospective Study

S. Christianto, Melita Sylviana, A. Hardianto
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Abstract

Introduction Ameloblastoma is common benign epithelial tumor of odontogenic origin. The presentation of ameloblastoma is unique as it locally aggressive tumor with high recurrence rate if not treated adequately. This study aimed to conduct retrospective study to analyze the characteristics and management of ameloblastoma in patient Oral and Maxillofacial Surgery at Hasan Sadikin General Hospital between periods of January 2020 – December 2020. Material and Method This was a retrospective, descriptive feature of all histopathologically diagnosed ameloblastoma during 2020. We took data from each patient such as demographic (gender, age), radiological features, histopatholoical diagnosis, location, management, defect and reconstruction of ameloblastoma. Result A total 23 patients were diagnosed with conventional ameloblastoma, including 11 plexiform (48%), ten follicular (43%), and two mixed types of plexiform-follicular (9%). Among them, 6 (21%) patients were treated conservatively (Enucleation and dredging) and 17 patients were treated radically with segmental resection in 9 (39%) patients, hemimandibulectomy in 5 (22%) patients, marginal resection in 2 (9%) patients, and hemimaxillectomy in one (4%) patient. Conclusion The common characteristic of ameloblastoma is follicular and plexiform ameloblastoma with the most predilection location in mandible region and the peak of incidence in third decades of life. Radical treatment is more often used to reduce recurrence rates, whereas conservative measures are normally preserved in children and adolescent. Keywords: Ameloblastoma, Epidemiology, Odontogenic, Tumour
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哈桑萨迪金总医院口腔颌面外科成釉细胞瘤的特点和处理:回顾性研究
成釉细胞瘤是一种常见的牙源性良性上皮肿瘤。成釉细胞瘤的表现是独特的,因为它是一种局部侵袭性肿瘤,如果治疗不当,复发率很高。本研究旨在进行回顾性研究,分析2020年1月至2020年12月期间哈桑萨迪金综合医院口腔颌面外科患者成釉细胞瘤的特征和处理。材料和方法回顾性分析2020年期间所有组织病理学诊断成釉细胞瘤的描述性特征。我们收集了每位患者的数据,如人口统计学(性别、年龄)、放射学特征、组织病理学诊断、位置、处理、成釉细胞瘤的缺陷和重建。结果23例确诊为常规成釉细胞瘤,其中丛状型11例(48%),滤泡型10例(43%),丛状-滤泡混合型2例(9%)。其中6例(21%)采用保守治疗(去核疏浚),17例采用根治性治疗,其中9例(39%)采用节段性切除,5例(22%)采用半下颌管切除术,2例(9%)采用边缘切除,1例(4%)采用半下颌管切除术。结论成釉细胞瘤的共同特征为滤泡状和丛状成釉细胞瘤,易发生于下颌骨,30岁为发病高峰。根治性治疗更常用于降低复发率,而保守措施通常保留在儿童和青少年中。关键词:成釉细胞瘤,流行病学,牙源性,肿瘤
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