Journal Basic Info

  • Impact Factor: 2.709**
  • H-Index: 11 
  • ISSN: 2474-1663
  • DOI: 10.25107/2474-1663
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Pancreatic Cancer
  •  Immunology
  •  Hormone Therapy
  •  Prostate Cancer
  •  Stomach Cancer
  •  Haemato-Oncology
  •  Kidney Cancer
  •  Breast Cancer

Abstract

Citation: Clin Oncol. 2018;3(1):1454.DOI: 10.25107/2474-1663.1454

Increased Risk of Male Breast Cancer with Prolactinoma: A Case Report

Michelle Abghari, Deimante Tamkus and Harvey Bumpers

Departments of Surgery and Medical Oncology, Michigan State University, CHM, USA

*Correspondance to: Harvey Bumpers 

 PDF  Full Text Editorial | Open Access

Abstract:

This case is reported of a 52 year-old male who, seventeen years after the treatment for a prolactinoma and over ten years after the onset of bilateral gynecomastia, developed left sided breast cancer. Ductal carcinoma in situ was found incidentally after he decided to have a left breast mass excised for symptomatic gynecomastia. Pathology reported a 1.0 cm, ductal carcinoma in situ, cribriform, grade 1, estrogen receptor (ER) positive, and progesterone receptor (PR) positive mass which later required a completion mastectomy. The patient was also consequently found to have a decrease in testosterone levels requiring high doses of testosterone replacement therapy. BRCA testing was recommended. In review of the patient’s breast cancer family history, only a paternal aunt was identified. The patient was considered a candidate for contra lateral total mastectomy due to high levels of testosterone replacement and concerns with estrogen conversion. However, genetic testing was found to be negative and endocrine therapy (tamoxifen) was initiated as the patient requested to be treated conservatively.

Keywords:

Male breast cancer; Breast cancer; Prolactinoma

Cite the Article:

Abghari M, Tamkus D, Bumpers H. Increased Risk of Male Breast Cancer with Prolactinoma: A Case Report. Clin Oncol. 2018; 3: 1454.

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