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中国年轻女性中同时存在的导管原位癌和叶状乳腺肿瘤:病例系列

Coexisting DCIS and phyllodes breast tumors in Young Chinese women: Case series.

作者信息

Sun Luona, Zhu Roger, Ginter Paula, Malik Manmeet, Sung Kap-Jae, Hughes J Melissa, Siegel Beth, Tsai Jacqueline

机构信息

Department of Surgery, New York Presbyterian Queens, United States.

Department of Surgery, New York Presbyterian Queens, United States.

出版信息

Int J Surg Case Rep. 2019;56:13-16. doi: 10.1016/j.ijscr.2019.01.045. Epub 2019 Feb 8.

DOI:10.1016/j.ijscr.2019.01.045
PMID:30798095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6389554/
Abstract

INTRODUCTION

Breast cystosarcoma phyllodes tumors are rare and can be benign or malignant. All sub-divisions of phyllodes tumor-benign, borderline and malignant, can harbor carcinomas, although the incidence is extremely rare.

METHODS

We present two nonconsecutive cases of coexisting ductal carcinoma in situ (DCIS) and phyllodes breast tumors in young patients.

METHODS & CASE PRESENTATION: Retrospective review of two patient's medical record was performed. CASE 1: 30-year-old female underwent excisional biopsy for 3.48 cm mass found on ultrasound. Pathology revealed malignant phyllodes tumor with positive margin. On re-excision, patient was found to have 1.5 cm area of ductal carcinoma in situ (DCIS) with positive margin. Patient then underwent re-reexicision of DCIS with negative margin. Patient underwent chemotherapy and tamoxifen for three years without evidence of disease. CASE 2: 30-year-old female presented with 1.3 cm lesion found on ultrasound which core needle biopsy revealed a fibroepithelial tumor. Patient subsequently underwent excision biopsy which found 1.5 cm benign phyllodes tumor and 3.5 mm DCIS within the phyllodes tumor with negative margins. Patient declined additional chemotherapy or hormonal therapy and is currently considering mastectomy.

CONCLUSION

Phyllodes tumors are rare and ones with a coexisting carcinoma are even less frequently encountered. The treatment plan can change upon diagnosis of the carcinoma via the pathology. Treatment should be guided by the type and stage of carcinoma detected which may include additional surgical resection and lymph node sampling.

摘要

引言

乳腺叶状囊肉瘤肿瘤罕见,可为良性或恶性。叶状肿瘤的所有亚分类——良性、交界性和恶性,都可能伴有癌,尽管其发生率极低。

方法

我们报告两例年轻患者同时存在导管原位癌(DCIS)和乳腺叶状肿瘤的非连续病例。

方法与病例报告

对两名患者的病历进行回顾性分析。病例1:一名30岁女性因超声发现3.48厘米肿块接受切除活检。病理显示为恶性叶状肿瘤,切缘阳性。再次切除时,发现患者有1.5厘米面积的导管原位癌(DCIS),切缘阳性。随后患者对DCIS进行再次切除,切缘阴性。患者接受了三年的化疗和他莫昔芬治疗,无疾病证据。病例2:一名30岁女性因超声发现1.3厘米病变就诊,粗针活检显示为纤维上皮肿瘤。患者随后接受切除活检,发现1.5厘米的良性叶状肿瘤以及叶状肿瘤内3.5毫米的DCIS,切缘阴性。患者拒绝进一步化疗或激素治疗,目前正在考虑乳房切除术。

结论

叶状肿瘤罕见,同时伴有癌的情况更少见。通过病理诊断出癌后,治疗方案可能会改变。治疗应根据检测到的癌的类型和分期来指导,可能包括额外的手术切除和淋巴结取样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2021/6389554/18a5937d1d09/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2021/6389554/cce8fc9f7eba/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2021/6389554/582da3211ceb/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2021/6389554/b0f5f60bf425/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2021/6389554/18a5937d1d09/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2021/6389554/cce8fc9f7eba/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2021/6389554/582da3211ceb/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2021/6389554/b0f5f60bf425/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2021/6389554/18a5937d1d09/gr4.jpg

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