[Difficult interpretation of combined serous neoplasia of the peritoneum and fallopian tube: clinical and morphological observation].

Q4 Medicine
V E Rodionov, A V Asaturova, Yu A Kirillov
{"title":"[Difficult interpretation of combined serous neoplasia of the peritoneum and fallopian tube: clinical and morphological observation].","authors":"V E Rodionov, A V Asaturova, Yu A Kirillov","doi":"10.17116/patol20268805161","DOIUrl":null,"url":null,"abstract":"<p><p>The lack of established criteria for the assessment, classification, and staging of rare tumors of the female reproductive organs represents a significant challenge in gynecologic oncology. We propose potential approaches to the assessment of such neoplasms using the example of combined serous neoplasia of the peritoneum and fallopian tube. In an 84-year-old female patient with verified endometrioid adenocarcinoma of the corpus uteri, histological examination of the surgical specimen revealed combined neoplasia of the greater omentum and fallopian tube. Immunohistochemical examination revealed positive expression of ER, p16 (heterogeneous reaction), and p53 (\"wild-type\"), and negative expression of WT1 and MLH1/PMS2. The omental and fallopian tube tumors demonstrated a WT1+/PAX8+/Ber-EP4+ immunophenotype with preserved expression of MMR proteins. Mutations in the NRAS, KRAS, or BRAF genes were not detected. Following a comprehensive analysis, a diagnosis of primary multiple malignancies was established: endometrioid adenocarcinoma of the uterine corpus G1 (MMR-deficient molecular subtype) and low-grade serous adenocarcinoma of the peritoneum with involvement of the greater omentum (invasive implants) and fallopian tube (non-invasive implants). This case highlights the need to analyze similar cases to refine international classifications and clinical guidelines.</p>","PeriodicalId":8548,"journal":{"name":"Arkhiv patologii","volume":"88 5","pages":"61-65"},"PeriodicalIF":0.0000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Arkhiv patologii","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17116/patol20268805161","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

The lack of established criteria for the assessment, classification, and staging of rare tumors of the female reproductive organs represents a significant challenge in gynecologic oncology. We propose potential approaches to the assessment of such neoplasms using the example of combined serous neoplasia of the peritoneum and fallopian tube. In an 84-year-old female patient with verified endometrioid adenocarcinoma of the corpus uteri, histological examination of the surgical specimen revealed combined neoplasia of the greater omentum and fallopian tube. Immunohistochemical examination revealed positive expression of ER, p16 (heterogeneous reaction), and p53 ("wild-type"), and negative expression of WT1 and MLH1/PMS2. The omental and fallopian tube tumors demonstrated a WT1+/PAX8+/Ber-EP4+ immunophenotype with preserved expression of MMR proteins. Mutations in the NRAS, KRAS, or BRAF genes were not detected. Following a comprehensive analysis, a diagnosis of primary multiple malignancies was established: endometrioid adenocarcinoma of the uterine corpus G1 (MMR-deficient molecular subtype) and low-grade serous adenocarcinoma of the peritoneum with involvement of the greater omentum (invasive implants) and fallopian tube (non-invasive implants). This case highlights the need to analyze similar cases to refine international classifications and clinical guidelines.

[腹膜和输卵管合并浆液性肿瘤的难解:临床和形态学观察]。
缺乏对女性生殖器官罕见肿瘤的评估、分类和分期的既定标准是妇科肿瘤学的一个重大挑战。我们以腹膜和输卵管合并浆液性肿瘤为例,提出评估此类肿瘤的潜在方法。一例84岁女性子宫内膜样腺癌患者,手术标本组织学检查显示大网膜和输卵管合并瘤变。免疫组化检查显示ER、p16(异质性反应)、p53(“野生型”)阳性表达,WT1、MLH1/PMS2阴性表达。大网膜和输卵管肿瘤表现为WT1+/PAX8+/Ber-EP4+免疫表型,并保留MMR蛋白的表达。未检测到NRAS、KRAS或BRAF基因的突变。综合分析后,诊断为原发性多发性恶性肿瘤:子宫体子宫内膜样腺癌G1 (mmr缺陷分子亚型)和腹膜低级别浆液性腺癌,累及大网膜(侵袭性植入物)和输卵管(非侵袭性植入物)。该病例强调需要分析类似病例,以完善国际分类和临床指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Arkhiv patologii
Arkhiv patologii Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
55
期刊介绍: The journal deals with original investigations on pressing problems of general pathology and pathologic anatomy, newest research methods, major issues of the theory and practice as well as problems of experimental, comparative and geographic pathology. To inform readers latest achievements of Russian and foreign medicine the journal regularly publishes editorial and survey articles, reviews of the most interesting Russian and foreign books on pathologic anatomy, new data on modern methods of investigation (histochemistry, electron microscopy, autoradiography, etc.), about problems of teaching, articles on the history of pathological anatomy development both in Russia and abroad.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书