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先天性颗粒细胞龈瘤呈现出一种免疫组织化学特征,使其有别于成人的颗粒细胞瘤。

Congenital granular cell epulis presents an immunohistochemical profile that distinguishes it from the granular cell tumor of the adult.

作者信息

Vered Marilena, Dobriyan Alex, Buchner Amos

机构信息

Department of Oral Pathology and Oral Medicine, Goldschleger School of Dental Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Virchows Arch. 2009 Mar;454(3):303-10. doi: 10.1007/s00428-009-0733-y. Epub 2009 Feb 11.

Abstract

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.

摘要

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。

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