Pleomorphic Adenoma of the Palate with Bizarre Ductal and Myoepithelial Cells: A Case Image.

IF 4.1
Katsutoshi Hirose, Masato Nakaguro, Kohei Kawamura, Taisuke Mori, Satoru Toyosawa
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Abstract

Background: Pleomorphic adenomas (PAs), the most common salivary gland tumors, are comprised of ductal epithelial and myoepithelial cells within a stromal background. A rare subset of PAs exhibits bizarre cells and 12q amplification involving HMGA2 and MDM2; in reported cases, bizarre cells have been confined to the myoepithelial component. We report the first case of a PA with bizarre-cytological features in both the ductal and myoepithelial components.

Case presentation: A 75-year-old woman presented with a palatal mass. Histology revealed a well-circumscribed biphasic tumor with marked nuclear pleomorphism in both luminal ductal and non-luminal myoepithelial cells. Despite the alarming atypia, mitotic activity was low, and neither necrosis nor invasive growth was observed. Immunohistochemically, luminal bizarre cells exhibited ductal characteristics, whereas non-luminal bizarre cells exhibited myoepithelial characteristics. Tumor cells were negative for androgen receptor and HER2 and showed a p53 wild-type expression pattern. The Ki-67 labeling index was < 5%, and the bizarre cells rarely tested positive. Molecular analysis demonstrated amplification of HMGA2 and MDM2, whereas no other pathogenic variants related to salivary gland tumors were detected. Complete excision was performed; no evidence of recurrence or metastasis was observed after 10 months.

Conclusion: Marked cytological atypia of bizarre cells in PA, even when involving ductal cells, may not necessarily indicate malignancy. This case highlights the value of integrating clinicopathological and genetic findings to better define PAs with bizarre cells and prevent overdiagnosis of carcinoma based on atypia alone.

腭多形性腺瘤伴奇异的导管和肌上皮细胞:一例图像。
背景:多形性腺瘤(PAs)是最常见的唾液腺肿瘤,由间质背景下的导管上皮细胞和肌上皮细胞组成。一个罕见的PAs亚群表现出奇怪的细胞和12q扩增,涉及HMGA2和MDM2;在报告的病例中,奇异细胞仅限于肌上皮成分。我们报告了第一例在导管和肌上皮成分中具有奇异细胞学特征的PA。病例介绍:一名75岁女性,出现腭部肿块。组织学显示一个界限清晰的双期肿瘤,在管腔和非管腔肌上皮细胞中都有明显的核多形性。尽管存在令人担忧的异型性,但有丝分裂活性低,未观察到坏死或侵袭性生长。免疫组织化学上,管腔奇异细胞表现出导管特征,而非管腔奇异细胞表现出肌上皮特征。肿瘤细胞雄激素受体和HER2均阴性,p53呈野生型表达。结论:PA中奇异细胞有明显的细胞学异型性,即使涉及到导管细胞,也不一定是恶性肿瘤。该病例强调了整合临床病理和遗传学结果的价值,以更好地定义具有奇异细胞的PAs,并防止仅基于异型性的过度诊断。
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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