一例罕见的眼睑原发性腺癌

D. L. Rotin, O. Paklina, E. I. Zakurdaev, I. O. Tin’kova
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引用次数: 0

摘要

介绍。摘要原发性眼睑皮肤黏液癌是一种罕见的皮肤腺癌。这种肿瘤很少转移,但经常复发。本研究的目的是描述一罕见的眼睑皮肤原发性黏液性癌的临床病例,并提出该病理的宏观、组织学和免疫组织学描述。临床病例。男,66岁,因下眼睑肿瘤求医。镜下见皮下淋巴结1.2 × 1.0 cm,黄褐色,切片呈胶状。显微镜检查显示肿瘤由黏液“湖”包围的上皮细胞岛组成。免疫组化检查显示肿瘤细胞中Ck7、雌激素、p53表达,Ck20不表达。根据肉眼、显微镜及免疫组化检查资料,诊断为原发性眼睑皮肤黏液癌。观察到的形态学征象可以将其与转移性肿瘤区分开来。原发性皮肤黏液性癌应与乳腺、肺、结肠等黏液性癌的转移相鉴别,这种肿瘤的宏观和微观征象是主观的。免疫组织化学检查是一种更可靠的诊断工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of primary adenocarcinoma of the eyelid
Introduction. primary mucinous carcinoma of the eyelid skin is a rare adenocarcinoma of skin glands. This tumor rarely metastasizes but frequently recurs.The study objective is to describe a rare clinical case of primary mucinous carcinoma of the eyelid skin, present macroscopic, histological and immunohistological descriptions of this pathology.Clinical case. male, 66 years old, sought medical care due to a neoplasm of the lower eyelid. macroscopically a subcutaneous node 1.2 × 1.0 cm was observed, of yellow-brown color, gelatinous in section. microscopic examination showed that the tumor consists of islands of epithelial cells surrounded by mucinous “lakes”. Immunohistochemical examination showed Ck7, estrogen, p53 expression in the tumor cells, as well as absence of Ck20 expression. Based on the data of macro-, microscopic and immunohistochemical examinations, primary mucinous carcinoma of the eyelid skin was diagnosed. Observed morphological signs of this tumor allow to differentiate it from cancer metastasis.Conclusion. primary mucinous carcinoma of the skin should be differentiated from metastasis of mucinous carcinoma of the breast, lung, colon, et al. macro- and microscopic signs of this tumor are subjective. Immunohistochemical examination is a more reliable diagnostic tool.
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