Primary pleomorphic breast sarcoma - a case report.

Q4 Dentistry Folia medica Pub Date : 2024-08-31 DOI:10.3897/folmed.66.e120391
Daniel Markov, Petar Uchikov, Pavel Timonov, Galabin Markov, Elena Poryazova
{"title":"Primary pleomorphic breast sarcoma - a case report.","authors":"Daniel Markov, Petar Uchikov, Pavel Timonov, Galabin Markov, Elena Poryazova","doi":"10.3897/folmed.66.e120391","DOIUrl":null,"url":null,"abstract":"<p><p>Primary mammary sarcomas are very rare, histologically heterogeneous non-epithelial malignant neoplasms. Primary undifferentiated pleomorphic sarcoma is a rare malignant mesenchymal tumor in the breast. It is characterized by marked cellular atypism and pleomorphism. Isolated cases with an aggressive course and poor prognosis have been commonly described in the literature. We present a rare case of a 62-year-old woman with an 18-cm solid tumor of the left breast, 6 months old, which grew rapidly during the last month. Physical examination and mammography revealed no enlarged lymph nodes in the left axilla. A total mastectomy was performed. The diagnosis of undifferentiated pleomorphic sarcoma is challenging due to the lack of specific immunohistochemical markers. It can only be made after excluding other types of soft tissue sarcomas. This report discusses the histopathological and immunohistochemical studies that were conducted. Our case is distinguished from others with the same diagnosis by the atypical clinical presentation, which is painless, and the spontaneous bleeding, as well as the large size of the tumor.</p>","PeriodicalId":12415,"journal":{"name":"Folia medica","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Folia medica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3897/folmed.66.e120391","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Dentistry","Score":null,"Total":0}
引用次数: 0

Abstract

Primary mammary sarcomas are very rare, histologically heterogeneous non-epithelial malignant neoplasms. Primary undifferentiated pleomorphic sarcoma is a rare malignant mesenchymal tumor in the breast. It is characterized by marked cellular atypism and pleomorphism. Isolated cases with an aggressive course and poor prognosis have been commonly described in the literature. We present a rare case of a 62-year-old woman with an 18-cm solid tumor of the left breast, 6 months old, which grew rapidly during the last month. Physical examination and mammography revealed no enlarged lymph nodes in the left axilla. A total mastectomy was performed. The diagnosis of undifferentiated pleomorphic sarcoma is challenging due to the lack of specific immunohistochemical markers. It can only be made after excluding other types of soft tissue sarcomas. This report discusses the histopathological and immunohistochemical studies that were conducted. Our case is distinguished from others with the same diagnosis by the atypical clinical presentation, which is painless, and the spontaneous bleeding, as well as the large size of the tumor.

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
原发性多形性乳腺肉瘤--病例报告。
原发性乳腺肉瘤是非常罕见的组织学异质性非上皮性恶性肿瘤。原发性未分化多形性肉瘤是一种罕见的乳腺恶性间质肿瘤。其特点是细胞明显不典型和多形性。文献中常描述一些病程凶险、预后不良的孤立病例。我们报告了一例罕见病例,患者是一名 62 岁女性,左侧乳房长有一个 18 厘米的实体瘤,发病已有 6 个月,最近一个月肿瘤生长迅速。体格检查和乳房 X 光检查显示左侧腋窝无肿大淋巴结。患者接受了全乳房切除术。由于缺乏特异性免疫组化标记,未分化多形性肉瘤的诊断具有挑战性。只有在排除其他类型的软组织肉瘤后才能做出诊断。本报告讨论了所进行的组织病理学和免疫组化研究。我们的病例由于临床表现不典型(无痛、自发性出血)和肿瘤体积较大而与其他诊断相同的病例有所区别。
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
Folia medica
Folia medica Medicine-Medicine (all)
CiteScore
1.00
自引率
0.00%
发文量
121
审稿时长
5 weeks
期刊最新文献
A review of alternative measurements in strain imaging for ventricular arrhythmia prediction. Attitudes and awareness related to cervical cancer vaccine. Clinical and echocardiographic characteristics of patients with atrial cardiomyopathy and their impact on prognosis. Congenital extrahepatic portosystemic shunt in a teenager: a case report. Correlating the genetic alterations and expression profile of the TRA2B gene in HNSCC and LUSC.
×
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