A Rare Case of the Malignant Phyllodes Breast Tumor - Case Report

Q3 Medicine
Kocic Svetlana, Vojinovic Radisa, Prijic-Plecevic Lidija
{"title":"A Rare Case of the Malignant Phyllodes Breast Tumor - Case Report","authors":"Kocic Svetlana, Vojinovic Radisa, Prijic-Plecevic Lidija","doi":"10.2478/sjecr-2022-0007","DOIUrl":null,"url":null,"abstract":"Abstract The phyllodes tumor (cystosarcoma phyllodes) is a rare fibroepithelial neoplasm presenting less than 1% of all breast tumors. Based on histologic features World Health Organization (WHO) classifies into benign, border line and malignant tumors (the rarest). Only around 5-15% of all malignant form cases metastasize hematogeneosly in the lung, bone and brain. Clinically are mostly presented the phyllodes tumor mostly presents as a rapid growth, palpabile, painless, elastic, oval or lobulated masses over 5 cm among women between 40 to 50 years old. On ultrasound and mammography these tumors usually resembles other round or oval benign lesions, mostly like fibroadenomas. These tumors on ultrasound and mammography usually resembles other round or oval benign tumors, mostly like fibroadenomas. Ultrasound guided core needle biopsiy (CNB) performed under ultrasound is a gold standard for palpabile breast masses. Surgical resection remains the gold standard of treatment. To date, there is no consensus regarding the recommendations for radiotherapy, hormonal therapy and systemic chemotherapy. We present the case of 30 years old woman, who noted a painless mass in her left breast, which was gradually increasing in size. Clinical, ultrasound and magnetic resonance examination confirmed the existence of tumor formation without the possibility of making an accurate diagnosis. Malignant phyllodes tumor was initially diagnosed by core biopsy. The patient underwent a radical modified mastectomy and postoperative radiotherapy. During the follow-up for the first 11 months, our patient has been feeling well without signs of local recurrence and metastasis. The aim of our case is to emphasize the importance of early diagnosis and treatment of this rare breast tumor. Treatment is based on the size and the extent of the mass with surgical resection and adequate margins extremely important in successful outcome. We present the case of 30 old woman, who noted a painless mass in her left breast, which was gradually increasing in size. She was diagnosed with ultrasound and magnetic resonance imaging and the diagnosis of the malignant phyllodes tumor was confirmed by patohistological verification.","PeriodicalId":21582,"journal":{"name":"Serbian Journal of Experimental and Clinical Research","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Serbian Journal of Experimental and Clinical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2478/sjecr-2022-0007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Abstract The phyllodes tumor (cystosarcoma phyllodes) is a rare fibroepithelial neoplasm presenting less than 1% of all breast tumors. Based on histologic features World Health Organization (WHO) classifies into benign, border line and malignant tumors (the rarest). Only around 5-15% of all malignant form cases metastasize hematogeneosly in the lung, bone and brain. Clinically are mostly presented the phyllodes tumor mostly presents as a rapid growth, palpabile, painless, elastic, oval or lobulated masses over 5 cm among women between 40 to 50 years old. On ultrasound and mammography these tumors usually resembles other round or oval benign lesions, mostly like fibroadenomas. These tumors on ultrasound and mammography usually resembles other round or oval benign tumors, mostly like fibroadenomas. Ultrasound guided core needle biopsiy (CNB) performed under ultrasound is a gold standard for palpabile breast masses. Surgical resection remains the gold standard of treatment. To date, there is no consensus regarding the recommendations for radiotherapy, hormonal therapy and systemic chemotherapy. We present the case of 30 years old woman, who noted a painless mass in her left breast, which was gradually increasing in size. Clinical, ultrasound and magnetic resonance examination confirmed the existence of tumor formation without the possibility of making an accurate diagnosis. Malignant phyllodes tumor was initially diagnosed by core biopsy. The patient underwent a radical modified mastectomy and postoperative radiotherapy. During the follow-up for the first 11 months, our patient has been feeling well without signs of local recurrence and metastasis. The aim of our case is to emphasize the importance of early diagnosis and treatment of this rare breast tumor. Treatment is based on the size and the extent of the mass with surgical resection and adequate margins extremely important in successful outcome. We present the case of 30 old woman, who noted a painless mass in her left breast, which was gradually increasing in size. She was diagnosed with ultrasound and magnetic resonance imaging and the diagnosis of the malignant phyllodes tumor was confirmed by patohistological verification.
乳腺叶状恶性肿瘤1例报告
叶状肿瘤(叶状囊肉瘤)是一种罕见的纤维上皮肿瘤,在所有乳腺肿瘤中占比不到1%。世界卫生组织(WHO)根据组织学特征将其分为良性、边缘性和恶性肿瘤(最罕见)。只有大约5-15%的恶性病例会在肺、骨和脑中发生血液转移。临床上多见于40 ~ 50岁女性,多表现为生长迅速、可触、无痛、弹性、卵形或分叶状肿块,体积大于5 cm。在超声和乳房x光检查中,这些肿瘤通常类似于其他圆形或椭圆形的良性病变,主要像纤维腺瘤。这些肿瘤在超声和乳房x光检查上通常类似于其他圆形或椭圆形的良性肿瘤,主要像纤维腺瘤。超声引导下进行的核心穿刺活检(CNB)是可触摸乳房肿块的金标准。手术切除仍然是治疗的金标准。迄今为止,关于放疗、激素治疗和全身化疗的建议尚未达成共识。我们提出的情况下,30岁的妇女,谁注意到一个无痛的肿块在她的左乳房,这是逐渐增加的大小。临床、超声及磁共振检查证实有肿瘤形成,但不能准确诊断。恶性叶状瘤最初诊断为核心活检。患者接受了根治性乳房切除术和术后放疗。在前11个月的随访中,我们的患者感觉良好,没有局部复发和转移的迹象。我们病例的目的是强调早期诊断和治疗这种罕见乳腺肿瘤的重要性。治疗是基于肿块的大小和范围,手术切除和足够的切缘对成功的结果非常重要。我们提出的情况下,30岁的妇女,谁注意到一个无痛的肿块在她的左乳房,这是逐渐增加的大小。经超声及磁共振检查,病理组织学证实为恶性叶状瘤。
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
自引率
0.00%
发文量
56
审稿时长
6 weeks
期刊介绍: Serbian Journal of Experimental and Clinical Research is a peer-reviewed, general biomedical journal. It publishes original basic and clinical research, clinical practice articles, critical reviews, case reports, evaluations of scientific methods, works dealing with ethical and social aspects of biomedicine as well as letters to the editor, reports of association activities, book reviews, news in biomedicine, and any other article and information concerned with practice and research in biomedicine, written in the English.
×
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:481959085
Book学术官方微信