Primary breast angiosarcoma in a male

Leena Kamat, Marilin Rosa, Robert Weinfurtner, Jennifer Drukteinis, Shannon Falcon, Bhavika Patel

Research output: Contribution to journalArticle

5 Scopus citations

Abstract

Angiosarcoma of the breast represent <1% of breast malignancies. It can arise de novo (primary) or following treatment for breast carcinoma (secondary). Primary breast angiosarcoma usually affects young women and is extremely rare in the male patient population. Imaging features can have a nonspecific appearance. Histologically, the diagnosis can be challenging, especially in small core needle biopsies. Mastectomy or wide local excision is the usual treatment for both forms of angiosarcoma. Prognosis and recurrence is worse with increasing grade of tumor. Herein, we discuss the rare occurrence of primary breast angiosarcoma in a man with history of immunodeficiency. Clinical, radiological and pathologic findings will be discussed.

Original languageEnglish (US)
Pages (from-to)545-548
Number of pages4
JournalBreast Journal
Volume21
Issue number5
DOIs
StatePublished - Jan 1 2015
Externally publishedYes

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Keywords

  • angiosarcoma
  • breast tumor
  • HIV
  • male

ASJC Scopus subject areas

  • Internal Medicine
  • Surgery
  • Oncology

Cite this

Kamat, L., Rosa, M., Weinfurtner, R., Drukteinis, J., Falcon, S., & Patel, B. (2015). Primary breast angiosarcoma in a male. Breast Journal, 21(5), 545-548. https://doi.org/10.1111/tbj.12453