Occult pleomorphic lobular breast carcinoma presenting exclusively as microangiopathic hemolytic anemia and circulating tumor cells: An autopsy case report

Human Pathology Reports Pub Date : 2025-03-01 Epub Date: 2024-12-15 DOI:10.1016/j.hpr.2024.300768
Lo Man Lai , Mercedeh Tajdar , Ann Janssens , Peter Vandenberghe , Gert De Hertogh , Wouter Van Den Bogaert
{"title":"Occult pleomorphic lobular breast carcinoma presenting exclusively as microangiopathic hemolytic anemia and circulating tumor cells: An autopsy case report","authors":"Lo Man Lai ,&nbsp;Mercedeh Tajdar ,&nbsp;Ann Janssens ,&nbsp;Peter Vandenberghe ,&nbsp;Gert De Hertogh ,&nbsp;Wouter Van Den Bogaert","doi":"10.1016/j.hpr.2024.300768","DOIUrl":null,"url":null,"abstract":"<div><div>Occult breast cancer (OBC) presents most commonly as solid tumor metastases when there is no clinically detectable primary breast lesion. We encountered a rare case of OBC in a 56-year-old woman mainly manifesting as cancer-related microangiopathic hemolytic anemia (CR-MAHA). She died suddenly during hospitalization and an autopsy was performed. Macroscopically, no primary tumor was identified. Microscopically, a massive number of circulating tumor cells (CTCs) were observed in almost all biopsied organs. The morphology and the immunohistochemical profile were consistent with pleomorphic lobular carcinoma (PLC) of the breast. Therefore, this is a rare case of OBC presenting exclusively in the form of CTCs originating from PLC. Awareness of this rare clinical presentation can aid in the correct diagnosis and appropriate patient management in the future.</div></div>","PeriodicalId":100612,"journal":{"name":"Human Pathology Reports","volume":"39 ","pages":"Article 300768"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Pathology Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772736X24000409","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/15 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Occult breast cancer (OBC) presents most commonly as solid tumor metastases when there is no clinically detectable primary breast lesion. We encountered a rare case of OBC in a 56-year-old woman mainly manifesting as cancer-related microangiopathic hemolytic anemia (CR-MAHA). She died suddenly during hospitalization and an autopsy was performed. Macroscopically, no primary tumor was identified. Microscopically, a massive number of circulating tumor cells (CTCs) were observed in almost all biopsied organs. The morphology and the immunohistochemical profile were consistent with pleomorphic lobular carcinoma (PLC) of the breast. Therefore, this is a rare case of OBC presenting exclusively in the form of CTCs originating from PLC. Awareness of this rare clinical presentation can aid in the correct diagnosis and appropriate patient management in the future.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
隐蔽性多形性小叶乳腺癌仅表现为微血管性溶血性贫血和循环肿瘤细胞:一个尸检病例报告
隐匿性乳腺癌(OBC)在临床上没有可检测到的原发性乳腺病变时,最常表现为实体瘤转移。我们遇到一个罕见的OBC病例,56岁女性,主要表现为癌症相关微血管病变溶血性贫血(CR-MAHA)。她在住院期间突然死亡,并进行了尸检。宏观上,未发现原发肿瘤。显微镜下,在几乎所有活检器官中观察到大量循环肿瘤细胞(ctc)。形态学和免疫组化特征符合乳腺多形性小叶癌(PLC)。因此,这是一种罕见的OBC仅以源自PLC的ctc形式呈现的情况。意识到这种罕见的临床表现可以帮助正确的诊断和适当的病人管理在未来。
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 去求助
来源期刊
CiteScore
0.60
自引率
0.00%
发文量
0
期刊最新文献
Rapidly enlarging breast mass during breastfeeding mimicking carcinoma: a case report and review of literature Pancolonic mast cell elevation correlates with IBS-like symptoms in ulcerative colitis patients achieving combined endoscopic and histologic remission: a retrospective case–control study A large and predominantly cystic breast adenomyoepithelioma in a 35-year-old female: A rare case report and mini review of literature A unique case of follicular large B-cell lymphoma arising in the background of thymic follicular hyperplasia Genetic and structural changes leading to symptomatic Currarino syndrome – case presentation with re-analyzation of 102 cases of MNX1 genetic change
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1