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乳头状黏液化生:子宫内膜黏液腺癌的一种独特前驱病变。

Papillary mucinous metaplasia: a distinct precursor of mucinous adenocarcinoma of the endometrium.

作者信息

Yoo Su Hyun

机构信息

Department of Pathology, Sanggye Baik Hospital, University of Inje College of Medicine Seoul, South Korea.

出版信息

Int J Clin Exp Pathol. 2022 Feb 15;15(2):83-87. eCollection 2022.

Abstract

Mucinous adenocarcinoma of the endometrium is heterogeneous, consisting of endometrioid adenocarcinoma composed of >50% mucinous cells, low-grade mucinous adenocarcinoma, microglandular adenocarcinoma, and gastric (gastrointestinal)-type adenocarcinoma. Previous studies have reported that papillary mucinous metaplasia is a possible precancerous lesion of mucinous adenocarcinoma with frequent mutations. Recently, we encountered a case of pure mucinous adenocarcinoma of the endometrium with concurrent papillary mucinous metaplasia in a 35-year-old woman. She underwent 6-month hormonal therapy for atypical endometrial hyperplasia. A follow-up biopsy led to a diagnosis of mucinous adenocarcinoma; therefore, total hysterectomy was performed. The tumor showed abundant intracytoplasmic mucin and mild-to-moderate cytologic atypia with papillary architecture. mutation analysis revealed a point mutation from GGT to GTT in codon 12. Although papillary mucinous metaplasia showed an overexpression of p16, especially in the intragrandular papillary tufts, and a low MKi67 labeling index, overt mucinous adenocarcinoma with a loss of P16 expression showed a high proliferating index of MKI67. The mass presented with stage ІA disease. During follow-up, the patient was stable and showed no recurrence. Considering the histologic similarity and incidence of mutations between papillary mucinous metaplasia and mucinous adenocarcinoma, papillary mucinous metaplasia may be a precancerous lesion for a subset of mucinous adenocarcinoma of the endometrium.

摘要

子宫内膜黏液腺癌具有异质性,由黏液细胞占比超过50%的子宫内膜样腺癌、低级别黏液腺癌、微腺体腺癌以及胃(胃肠道)型腺癌组成。既往研究报道,乳头状黏液化生是黏液腺癌可能的癌前病变,且常有基因突变。最近,我们遇到一例35岁女性的纯子宫内膜黏液腺癌,同时伴有乳头状黏液化生。她曾因非典型子宫内膜增生接受了6个月的激素治疗。后续活检诊断为黏液腺癌;因此,实施了全子宫切除术。肿瘤表现为胞质内黏液丰富,具有乳头状结构,细胞学异型性为轻度至中度。基因突变分析显示第12密码子存在从GGT到GTT的点突变。尽管乳头状黏液化生显示p16过表达,尤其是在腺内乳头状簇中,且MKi67标记指数较低,但P16表达缺失的明显黏液腺癌显示MKI67增殖指数较高。该肿块表现为ⅠA期疾病。随访期间,患者病情稳定,无复发。考虑到乳头状黏液化生与黏液腺癌之间的组织学相似性和基因突变发生率,乳头状黏液化生可能是一部分子宫内膜黏液腺癌的癌前病变。

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