Siar C H, Ng K H
Department of Oral Pathology, Oral Medicine and Periodontology, Faculty of Dentistry, University of Malaya, Kuala Lumpur, Malaysia.
J Nihon Univ Sch Dent. 1993 Jun;35(2):134-8. doi: 10.2334/josnusd1959.35.134.
Granular cell ameloblastoma (GCA) is a well recognized variant of follicular ameloblastoma with extensive granular cell change. In contrast, plexiform granular cell odontogenic tumor (PGCOT) is a rare and recently described lesion characterized histologically by a monophasic plexiform pattern of granular cells. In this paper, two cases of an unusual granular cell odontogenic tumor exhibiting combined features of these two entities are described along with their immunohistochemical characteristics. The granular cells of both the GCA and PGCOT areas showed similar patterns of expression for keratin and S-100, which differed from those of typical ameloblastoma. No reactivity for desmin or vimentin was noted. The histomorphologic and immunohistochemical features of these hybrid tumors suggest that the granular cells present have a common origin, most probably the odontogenic epithelium.
颗粒细胞成釉细胞瘤(GCA)是滤泡性成釉细胞瘤一种广为人知的变体,伴有广泛的颗粒细胞改变。相比之下,丛状颗粒细胞牙源性肿瘤(PGCOT)是一种罕见的、最近才被描述的病变,其组织学特征为颗粒细胞的单相丛状模式。本文描述了两例表现出这两种实体联合特征的不寻常颗粒细胞牙源性肿瘤病例及其免疫组化特征。GCA和PGCOT区域的颗粒细胞对角蛋白和S-100显示出相似的表达模式,这与典型成釉细胞瘤不同。未观察到结蛋白或波形蛋白的反应性。这些混合性肿瘤的组织形态学和免疫组化特征表明,所呈现的颗粒细胞具有共同的起源,很可能是牙源性上皮。