ArticleWorld journal of oncology2014
Primary Angiosarcoma of the Breast: A Case Report and Review of Literature.
Article in World journal of oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 15 citations in OpenAlex.
- An Atypical Presentation of Cutaneous Angiosarcoma: A Diagnostic Challenge in an End-Stage Renal Disease Patient.Cureus · 2026Article
- Primary Angiosarcoma of Breast: a Case Series of Rare Disease.Indian journal of surgical oncology · 2024Article
- Primary Angiosarcoma of the Breast: A Rare Case Report in Postmenopausal Women.The Indian journal of radiology & imaging · 2022Article
- A rare presentation of pregnancy associated primary angiosarcoma of the breasts.Radiology case reports · 2022Article
- A case of primary breast angiosarcoma with multiple discontinuous small lesions.Surgical case reports · 2019Article
- Primary Angiosarcoma Of the Breast: A Case Report.Journal of radiology case reports · 2019Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Angiosarcoma of the breast (ASB) is a rare but aggressive tumor with very poor prognosis. It is important to recognize this tumor early and to distinguish between primary and secondary ASB. While mammograms frequently miss these lesions, ultrasound and MRI show promise as imaging modalities. In spite of characteristic features described on pathology, misdiagnosis is common, with over 35% tumors initially thought to be benign. We present the case of a 32-year-old woman with a history of bilateral reduction mammoplasty who presented with a non-tender lump in her right breast. After repeated aspirations and biopsies, a diagnosis of primary ASB was made. She underwent bilateral simple mastectomies followed by adjuvant chemo-therapy and radiation. While surgery is the mainstay of treatment, roles of radiation and chemo-therapy are still evolving; we review the literature and discuss the decision pathways for diagnosis and management of this rare tumor.
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Registered trials
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