Infiltrating lobular carcinoma of LUMB HER2+ subtype with rhabdoid feature coexisting with synchronous malignant transformation of phyllodes tumor: An exceedingly rare clinicopathological characteristic in Vietnam.

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2024-08-05 eCollection Date: 2024-01-01 DOI:10.1177/20363613241271665
Tu Anh Do, Nhung Thi Mai, Duong Ngoc Nguyen, Khoa Hong Pham, Duc Thanh Le, Hung Van Pham, Chu Van Nguyen
{"title":"Infiltrating lobular carcinoma of LUMB HER2+ subtype with rhabdoid feature coexisting with synchronous malignant transformation of phyllodes tumor: An exceedingly rare clinicopathological characteristic in Vietnam.","authors":"Tu Anh Do, Nhung Thi Mai, Duong Ngoc Nguyen, Khoa Hong Pham, Duc Thanh Le, Hung Van Pham, Chu Van Nguyen","doi":"10.1177/20363613241271665","DOIUrl":null,"url":null,"abstract":"<p><p>The transformation of a benign phyllodes tumor (PT) into a malignant PT and/or carcinoma is extremely uncommon. We present a case of a 66-year-old female with a huge mass on the left breast which was successfully removed by surgical resection. The pathological diagnosis was infiltrating lobular carcinoma with pure rhabdoid features and the malignant transformation of a benign phyllodes tumor. The first time this rare case was reported, it is demonstrated a special phenomenon through the synchronous transformation of PT grades and the carcinomatous transformation of PT.</p>","PeriodicalId":46078,"journal":{"name":"Rare Tumors","volume":"16 ","pages":"20363613241271665"},"PeriodicalIF":0.9000,"publicationDate":"2024-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11301723/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rare Tumors","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/20363613241271665","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The transformation of a benign phyllodes tumor (PT) into a malignant PT and/or carcinoma is extremely uncommon. We present a case of a 66-year-old female with a huge mass on the left breast which was successfully removed by surgical resection. The pathological diagnosis was infiltrating lobular carcinoma with pure rhabdoid features and the malignant transformation of a benign phyllodes tumor. The first time this rare case was reported, it is demonstrated a special phenomenon through the synchronous transformation of PT grades and the carcinomatous transformation of PT.

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
LUMB HER2+亚型浸润性小叶癌伴有横纹肌样特征,并与植物瘤同步恶变并存:越南极为罕见的临床病理特征。
良性蝶形瘤(PT)转变为恶性蝶形瘤和/或癌的情况极为罕见。我们报告了一例 66 岁女性的病例,她的左侧乳房有一个巨大肿块,手术切除后肿块被成功切除。病理诊断为具有纯横纹肌样特征的浸润性小叶癌和良性蝶形花瘤的恶性转化。这是首次报道这种罕见病例,它通过 PT 级的同步转化和 PT 的癌变展示了一种特殊现象。
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
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
期刊最新文献
Diagnosis and management of benign secreting pancreatic insulinoma: What's new? 4 case report. Primary ovarian peripheral primitive neuroectodermal tumor presented with breast metastasis; Case report. Durable disease regression with copanlisib treatment in PI3K-mutated metastasizing ameloblastoma: A case report. Reading level, acuity, and speed evaluation among retinoblastoma survivors: A prospective case series. A rare case of granular cell tumor affecting the upper back in a child.
×
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:481959085
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