Guo Xin, Watanabe Jiro, Nakatani Hiroaki, Fukushima Kei, Yamada Sohsuke
Department of Pathology and Laboratory Medicine, Kanazawa Medical University, Kahoku, Japan.
Department of Pathology, Kanazawa Medical University Hospital, Kahoku, Japan.
SAGE Open Med Case Rep. 2020 Oct 8;8:2050313X20940567. doi: 10.1177/2050313X20940567. eCollection 2020.
Myoepitheliomas account for approximately 1.5% of all salivary gland tumors and arise most frequently from the parotid gland. Recently, a new myoepithelioma variant, called mucinous myoepithelioma, has attracted widespread attention. These tumors are recognized as a unique subtype of myoepithelioma, characterized by the presence of abundant mucin. We herein report the findings of an 86-year-old Japanese woman who presented with a hard mass of the right parotid gland behind her right ear which was gradually increasing in size. The patient had undergone a fine-needle aspiration biopsy 4 years earlier, and a cytological evaluation of a biopsy specimen had shown features of pleomorphic adenoma. A resection was thus performed and the tissue was found to be an encapsulated, soft and solid mass, and the cut surface was observed to be a capsulated and well-defined tumor lesion with myxoid-looking foci of gray-white coloration. Microscopic examination revealed that this lesion was composed of a proliferation of bland-looking epithelial and myoepithelial cells, arranged in a solid or reticular growth fashion in an abundant myxomatous or hyalinized stroma. These neoplastic epithelial cells had centrally located small nuclei with fine chromatin and abundant clear to eosinophilic cytoplasm, often containing mucin in a uniform pattern. Immunohistochemical staining demonstrated the tumor cells to be positive for AE1/AE3, S-100 and mucicarmine. Our findings suggest this case to be one myoepithelioma variant of mucinous myoepithelioma, and more experience related to this myoepithelioma variant is necessary to better understand its biological behavior and make an accurate diagnosis for a proper treatment.
肌上皮瘤约占所有涎腺肿瘤的1.5%,最常发生于腮腺。最近,一种新的肌上皮瘤变体,称为黏液性肌上皮瘤,引起了广泛关注。这些肿瘤被认为是肌上皮瘤的一种独特亚型,其特征是存在大量黏液。我们在此报告一名86岁日本女性的病例,她右耳后右侧腮腺出现一个硬块,且肿块大小逐渐增大。该患者4年前曾接受细针穿刺活检,活检标本的细胞学评估显示为多形性腺瘤特征。因此进行了切除术,发现组织为一个包膜完整、质地软硬不均的肿块,切面观察为一个包膜完整、边界清晰的肿瘤病变,有灰白色黏液样病灶。显微镜检查显示,该病变由外观温和的上皮细胞和肌上皮细胞增生组成,在丰富的黏液瘤样或玻璃样变性基质中呈实性或网状生长方式排列。这些肿瘤上皮细胞有位于中央的小核,染色质细腻,胞质丰富、清亮至嗜酸性,常均匀含有黏液。免疫组化染色显示肿瘤细胞AE1/AE3、S-100和黏液卡红呈阳性。我们的研究结果表明该病例为黏液性肌上皮瘤的一种肌上皮瘤变体,需要更多关于这种肌上皮瘤变体的经验,以更好地了解其生物学行为并做出准确诊断以便进行恰当治疗。