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    Intracystic papillary carcinoma in a male as a rare presentation of breast cancer: a case report and literature review.

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    Authors
    Romics, Laszlo
    O'Brien, M Emmet
    Relihan, Norma
    O'Connell, Fionnuala
    Redmond, H Paul
    Affiliation
    Department of Surgery, Cork University Hospital, University College Cork, Wilton Road, Cork, Ireland. Laszlo.Romics@umassmed.edu.
    Issue Date
    2009
    
    Metadata
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    Citation
    Intracystic papillary carcinoma in a male as a rare presentation of breast cancer: a case report and literature review. 2009, 3:13 J Med Case Reports
    Journal
    Journal of medical case reports
    URI
    http://hdl.handle.net/10147/200771
    DOI
    10.1186/1752-1947-3-13
    PubMed ID
    19144122
    Additional Links
    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2635376/pdf/1752-1947-3-13.pdf
    http://www.jmedicalcasereports.com/content/pdf/1752-1947-3-13.pdf
    Abstract
    The term "intracystic papillary ductal carcinoma in situ" has recently changed and is now more appropriately referred to "intracystic papillary carcinoma". Intracystic papillary carcinoma in men is an extremely rare disease with only a few case presentations published in the literature so far.
    We discuss a case of a 44-year-old Caucasian man with an intracystic papillary carcinoma treated with simple mastectomy, sentinel lymph-node biopsy and contralateral risk-reducing mastectomy. These were followed by adjuvant radiotherapy of the breast.
    Triple assessment (i.e. clinical examination and radiological and histological assessment) with a high level of clinical suspicion is necessary to diagnose intracystic papillary carcinoma in men due to its rarity. Furthermore, genetic testing and risk-reducing mastectomy should also be considered in cases of a strong family history for male breast cancer.
    Item Type
    Article
    Language
    en
    ISSN
    1752-1947
    ae974a485f413a2113503eed53cd6c53
    10.1186/1752-1947-3-13
    Scopus Count
    Collections
    Cork University Hospital

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