Siriwardena B S M S, Goh Y C, Tilakaratne W M
University of Peradeniya, Faculty of Dental Sciences, Department of Oral Pathology, Sri Lanka.
Universiti Malaya, Faculty of Dentistry, Department of Oral and Maxillofacial Clinical Sciences, Malaysia.
Malays J Pathol. 2025 Aug;47(2):253-261.
Ameloblastoma is a benign but locally aggressive odontogenic tumour broadly divided into conventional, unicystic, peripheral, adenoid and metastasising types. The first three entities compose the majority and especially the conventional type which has different histopathological subtypes such as follicular, plexiform, acanthomatous, granular cell, basal cell and desmoplastic have been described. We report the largest series of ameloblastoma in a single study to analyse the demographic characteristics according to histopathological subtypes of ameloblastoma.
1,312 cases of ameloblastoma reported from two centres in Sri Lanka and Malaysia were analysed according to age, site and histopathological subtype.
Of the total of 1,312 cases, the mean age for conventional ameloblastoma (excluding desmolastic subtype) was 36.82±16.57. It was 46.3±15.21 for categorisewhile peripheral and unicystic ameloblastoma occurred at 40.77±16.35 and 31.00±17.37, respectively. Ninety percent of the cases were in the mandible (p=0.00001) with significant predilection for the right side. Unicystic and plexiform subtypes were mostly seen in the 11-20 age group while the desmoplastic subtype was seen in the 51-60 age group. The commonesthistological subtype was follicular subtype and acanthomatous changes were observed predominately in combination with follicular subtype. Majority of the acanthomatous subtype was observed inposterior mandible (p=0.00001). The frequency of luminal (243) and mural (246) subtypes werealmost similar.
This study provides a comprehensive demographic detail of differenthistological subtypes of ameloblastoma using the largest sample in the literature. The present findingswill be helpful in classification and understanding of different subtypes of the tumours.
成釉细胞瘤是一种良性但具有局部侵袭性的牙源性肿瘤,大致可分为传统型、单囊性、外周型、腺样型和转移性类型。前三种类型占大多数,尤其是传统型,它具有不同的组织病理学亚型,如滤泡型、丛状型、棘皮瘤型、颗粒细胞型、基底细胞型和促结缔组织增生型。我们报告了一项单一研究中最大系列的成釉细胞瘤病例,以根据成釉细胞瘤的组织病理学亚型分析人口统计学特征。
对来自斯里兰卡和马来西亚两个中心报告的1312例成釉细胞瘤病例,根据年龄、部位和组织病理学亚型进行分析。
在总共1312例病例中,传统型成釉细胞瘤(不包括促结缔组织增生亚型)的平均年龄为36.82±16.57岁。促结缔组织增生型为46.3±15.21岁,而外周型和单囊性成釉细胞瘤分别发生于40.77±16.35岁和31.00±17.37岁。90%的病例位于下颌骨(p = 0.00001),右侧有明显偏好。单囊性和丛状亚型多见于11 - 20岁年龄组,而促结缔组织增生亚型见于51 - 60岁年龄组。最常见的组织学亚型是滤泡型,棘皮瘤样改变主要与滤泡型同时出现。大多数棘皮瘤型见于下颌骨后部(p = 0.00001)。管腔内型(243例)和壁型(246例)的频率几乎相似。
本研究使用文献中最大的样本,提供了成釉细胞瘤不同组织学亚型的全面人口统计学细节。目前的研究结果将有助于对肿瘤不同亚型进行分类和理解。