Periductal stromal tumor of breast: a case report and a review of literature.

Korean Journal of Pathology Pub Date : 2014-12-01 Epub Date: 2014-12-31 DOI:10.4132/KoreanJPathol.2014.48.6.442
Salma L Abbasi, Kate McNamara, Mohammed S Absar, Alison Darlington, Francene Clucas, Sami Titi
{"title":"Periductal stromal tumor of breast: a case report and a review of literature.","authors":"Salma L Abbasi, Kate McNamara, Mohammed S Absar, Alison Darlington, Francene Clucas, Sami Titi","doi":"10.4132/KoreanJPathol.2014.48.6.442","DOIUrl":null,"url":null,"abstract":"Periductal stromal tumor (PDST) is a rare biphasic tumor of the breast that exhibits low-grade malignancy and intermediate behavior. It is characterized by proliferation of atypical spindle cells surrounding benign mammary ducts and infiltrating adjacent adipose tissue. PDST is distinguished from phyllodes tumor by its lack of leaf-like architecture; however, it is still unclear whether PDST is a separate entity or a certain spectrum of phyllodes tumor [1,2]. Its therapeutic management is based on wide surgical excision with tumor-free margins. \n \nWe report the case of a 20-year-old female who presented with a lump in her left breast with clinical features mimicking fibroadenoma. Excisional biopsy was performed because the mass gradually enlarged and became painful. On histological examination a biphasic tumor composed of benign epithelial ducts surrounded by proliferation of spindle cells with dense hyperchromatic nuclei and mild-to-moderate atypia was found. Stromal overgrowth, variable stromal cellularity and myxoid background were evident. A diagnosis of PDST was established after extensive sampling and immunohistochemical analysis. Our patient was treated with surgical resection and has been recurrence-free for more than 38 months.","PeriodicalId":49936,"journal":{"name":"Korean Journal of Pathology","volume":"48 6","pages":"442-4"},"PeriodicalIF":0.0000,"publicationDate":"2014-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4132/KoreanJPathol.2014.48.6.442","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Korean Journal of Pathology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4132/KoreanJPathol.2014.48.6.442","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2014/12/31 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4

Abstract

Periductal stromal tumor (PDST) is a rare biphasic tumor of the breast that exhibits low-grade malignancy and intermediate behavior. It is characterized by proliferation of atypical spindle cells surrounding benign mammary ducts and infiltrating adjacent adipose tissue. PDST is distinguished from phyllodes tumor by its lack of leaf-like architecture; however, it is still unclear whether PDST is a separate entity or a certain spectrum of phyllodes tumor [1,2]. Its therapeutic management is based on wide surgical excision with tumor-free margins. We report the case of a 20-year-old female who presented with a lump in her left breast with clinical features mimicking fibroadenoma. Excisional biopsy was performed because the mass gradually enlarged and became painful. On histological examination a biphasic tumor composed of benign epithelial ducts surrounded by proliferation of spindle cells with dense hyperchromatic nuclei and mild-to-moderate atypia was found. Stromal overgrowth, variable stromal cellularity and myxoid background were evident. A diagnosis of PDST was established after extensive sampling and immunohistochemical analysis. Our patient was treated with surgical resection and has been recurrence-free for more than 38 months.

Abstract Image

Abstract Image

Abstract Image

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
乳腺导管周围间质瘤1例报告并文献复习。
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
Korean Journal of Pathology
Korean Journal of Pathology 医学-病理学
自引率
0.00%
发文量
0
审稿时长
6-12 weeks
期刊最新文献
Malignant perivascular epithelioid cell tumor of the uterus with lung metastasis. Lymphoepithelioma-like Carcinoma of the Renal Pelvis: A Case Report and Review of the Literature. Supratentorial hemangioblastoma with unusual features. A rare case of mesothelioma showing micropapillary and small cell differentiation with aggressive behavior. Hybrid granular cell tumor/perineurioma.
×
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