[Granular cell tumor and congenital epulis. Histochemical and immunohistochemical of 58 cases].

V Billeret-Lebranchu, E Martin de la Salle, B Vandenhaute, M Lecomte-Houcke
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Abstract

56 cases of granular cell tumour and 2 cases of granular cell congenital epulis have been studied morphologically, histochemically and immunohistochemically. The subject of this study is to evaluate the diagnosis interest of the PAS stain, determine the positivity of 4 antibodies (vimentin, NSE, PS100, NK1/C3) and confirm or not the neuroectodermic origin. The study showed that the microscopic findings are often sufficient. When the diagnosis is less evident, the PAS stain is not discriminant, but we can use the immunohistochemistry study: we confirmed the positivity of the 4 antibodies, but PS100 and NK1/C3 are the most constant. Only the 2 cases of granular cell congenital epulis always show negative immunoreactivity with S100 protein. About the histogenesis, our study confirm the neurogenic origin, but the hypothesis of a non neoplastic nature is raised.

颗粒细胞瘤和先天性肾盂。58例组织化学及免疫组织化学分析[j]。
本文对56例颗粒细胞瘤和2例颗粒细胞先天性脓包进行了形态学、组织化学和免疫组织化学研究。本研究的目的是评估PAS染色的诊断价值,确定4种抗体(vimentin、NSE、PS100、NK1/C3)的阳性,并确定是否为神经外胚层来源。研究表明,显微镜下的发现往往是足够的。当诊断不明显时,PAS染色不能鉴别,但我们可以使用免疫组织化学研究:我们证实了4种抗体的阳性,但PS100和NK1/C3是最恒定的。只有2例颗粒细胞型先天性瞳孔对S100蛋白的免疫反应均为阴性。关于组织发生,我们的研究证实了神经源性起源,但提出了非肿瘤性的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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