Vera-Sirera Beatriz, Zabala Pablo, Aviño-Mira Carlos, Vera-Sempere Francisco J
Department of Stomatology, University of Valencia, Valencia, Spain.
Department of Service of Gynecology, Hospital Nisa Pardo, Aravaca, Madrid, Spain.
J Oral Maxillofac Pathol. 2014 Sep-Dec;18(3):437-41. doi: 10.4103/0973-029X.151343.
Granular cell tumor (GCT) usually occurs as a single tumor, although sometimes multiple lesions can occur. In present report we analyze the clinicopathological and immunohistochemical features of a multiple GCT involving the tongue of a 14-year-old girl, with no other abnormalities, with a metachronous occurrence of a second GCT in vulva, after a period of 10 years. Both tumors revealed S-100, vimentin and CD57 positivity. In addition, over expression of calretinin was observed in tumor cells located in the vicinity of pseudoepitheliomatous hyperplasia (PEH) of the tongue. Tumor vasculature situated close to the PEH showed marked CD105 reactivity, data not described so far, suggesting an interaction between PEH cells and underlying stroma, since GCT completely lacks CD105 vessels. Our study emphasizes that patients with GCT, especially young patients, should be followed long-term, looking for multiple tumors or other abnormalities suggestive of a systemic syndrome, given the associations described in multiple GCT.
颗粒细胞瘤(GCT)通常以单发肿瘤形式出现,不过有时也会出现多个病灶。在本报告中,我们分析了一名14岁女孩舌部多发GCT的临床病理及免疫组化特征,该女孩无其他异常情况,10年后在外阴出现了第二例异时性GCT。两个肿瘤均显示S-100、波形蛋白和CD57阳性。此外,在舌部假上皮瘤样增生(PEH)附近的肿瘤细胞中观察到钙视网膜蛋白过表达。靠近PEH的肿瘤血管显示出明显的CD105反应性,这一数据此前未见报道,提示PEH细胞与下层基质之间存在相互作用,因为GCT完全缺乏CD105血管。我们的研究强调GCT患者,尤其是年轻患者,鉴于多发GCT中所描述的关联,应长期随访,以寻找多发肿瘤或其他提示全身性综合征的异常情况。