Vered Marilena, Dobriyan Alex, Buchner Amos
Department of Oral Pathology and Oral Medicine, Goldschleger School of Dental Medicine, Tel Aviv University, Tel Aviv, Israel.
Virchows Arch. 2009 Mar;454(3):303-10. doi: 10.1007/s00428-009-0733-y. Epub 2009 Feb 11.
Congenital granular cell epulis (CGCE), a rare benign lesion arising from the mucosa of the alveolar ridges of the jaws in newborns, has a clinical course characterized by lack of further growth after birth. Histomorphologically, it resembles a granular cell tumor (GCT) of the adult. The histogenesis of this lesion is unclear. We submitted a series of five CGCEs to a large panel of antibodies in order to trace the origin of the constituent granular cells. The resultant immunohistochemical profile showed positivity of these cells to vimentin, NKI/C3, and PGP9.5. This does not confirm any particular cell type for the histogenetic origin of CGCE but may rather reflect a local metabolic or reactive change, providing supporting evidence that the lesion is of a non-neoplastic nature. In addition, the granular cells were non-reactive for S-100, NGFR/p75, and inhibin-alpha, which further contributes to the distinction between a CGCE and the adult GCT.
先天性颗粒细胞龈瘤(CGCE)是一种罕见的良性病变,发生于新生儿颌骨牙槽嵴黏膜,其临床病程特点是出生后不再进一步生长。组织形态学上,它类似于成人的颗粒细胞瘤(GCT)。该病变的组织发生尚不清楚。我们对一系列5例先天性颗粒细胞龈瘤进行了大量抗体检测,以追踪组成颗粒细胞的起源。免疫组化结果显示这些细胞对波形蛋白、NKI/C3和PGP9.5呈阳性反应。这并未证实先天性颗粒细胞龈瘤组织发生起源的任何特定细胞类型,而可能反映的是局部代谢或反应性改变,为该病变为非肿瘤性性质提供了支持证据。此外,颗粒细胞对S-100、NGFR/p75和抑制素-α无反应,这进一步有助于区分先天性颗粒细胞龈瘤和成人颗粒细胞瘤。