Evidence map›Paper›PMID 41808134›Full record

ArticleBMC women's health2026

Atypical ultrasonic manifestation of dermatofibrosarcoma protuberans in a female patient: a case report of hyperechoic type and reflection on diagnosis and treatment.

Fang Chen, Xiaoyan Zhao, Yifan Jiang, Wanting Shao, Haidong Cui

Abstract readCase Reports
In one paragraph

Article in BMC women's health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Fang ChenDepartment of Nursing, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, 310003, P.R. China.
Xiaoyan ZhaoDepartment of Nursing, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, 310003, P.R. China.
Yifan JiangDivision of Hepatobiliary and Pancreatic Surgery, Department of Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, 310003, P.R. China.
Wanting ShaoDivision of Breast Surgery, Department of Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, 310003, P.R. China.
Haidong CuiDivision of Breast Surgery, Department of Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, 310003, P.R. China. 1321159@zju.edu.cn.

Funding

Zhejiang Province Traditional Chinese Medicine Science and Technology Program 2024ZL090
6 · The paper itself

Abstract

backgroundThe initial diagnosis of dermatofibrosarcoma protuberans (DFSP) can be extremely challenging in the absence of confirmatory pathological examination combined with immunohistochemical staining. Clinically, DFSP most frequently arises in the trunk, extremities, and head and neck region, while mammary DFSP is exceptionally rare. CASE PRESENTATION: A 22-year-old female presented with a two-week history of a right breast mass. Bilateral breast ultrasound identified a hyperechoic mass within the subcutaneous fat layer of the right breast, with no definite space-occupying lesion observed in the mammary glandular tissue. Based on the imaging features, the mass was initially suspected to be a lipoma, and the patient subsequently underwent lumpectomy. However, Postoperative pathological examination revealed a spindle cell soft tissue tumor, which was subsequently confirmed as DFSP through immunohistochemistry and molecular studies. Following a multidisciplinary team (MDT) consultation involving breast surgery, pathology, medical oncology, and radiology, the patient underwent wide local excision.

conclusionWe herein present a rare case of atypical breast DFSP with hyperechoic manifestations, which easily leads to diagnostic confusion with common benign breast lesions like lipoma. Accordingly, we emphasize a comprehensive diagnostic approach including clinical, imaging, and pathological evaluations is imperative for the accurate diagnosis of DFSP. However, the dual physical and psychological burden carried by young female patients should not be overlooked. It’s equally important to focus on their physical recovery and their emotional needs to optimize overall treatment outcomes.

Indexed as

Breast NeoplasmsDermatofibrosarcomaSkin NeoplasmsDiagnosis, DifferentialFemaleHumansLipomaUltrasonographyUltrasonography, MammaryYoung AdultBreast neoplasmsCD34Dermatofibrosarcoma protuberansPDGFSurgery

Identifiers

PMID41808134
PMCPMC13088696

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