Korean J Pathol.  2012 Apr;46(2):169-176.

The Clinicopathologic Features of Molecular Apocrine Breast Cancer

Affiliations
  • 1Department of Pathology, Severance Hospital, Yonsei University Health System, Yonsei University College of Medicine, Seoul, Korea. kjs1976@yuhs.ac

Abstract

BACKGROUND
To elucidate the clinicopathologic features and their implications on the immunohistochemistry in cases of molecular apocrine breast cancer (MABC).
METHODS
Immunohistochemical (IHC) staining for estrogen receptor (ER), human epidermal growth factor receptor 2 (HER-2), cytokeratin (CK) 5/6, epidermal growth factor receptor (EGFR), androgen receptor (AR), gamma-glutamyltrasferase 1 (GGT1) and Ki-67 was performed on tissue microarray breast cancer samples from 204 patients. Phenotypes of breast cancer were divided based on the IHC status of ER, AR and GGT1 into the following: luminal type, ER positive and AR and/or GGT1 positive; basal type, ER, AR, and GGT1 negative; non-basal type, ER positive and AR and GGT1 negative; and MABC type, ER negative and AR and/or GGT1 positive.
RESULTS
In our series of patients (n=204), there were 26 cases of MABC. Besides, there were 18, 60, and 100 cases of luminal type, basal type and non-basal type, respectively. The MABC demonstrated apocrine histology and a higher prevalence of HER-2 positivity than other phenotypes. With the basal type, the MABC manifested a more frequent expression of CK5/6 and EGFR and a higher Ki-67 index than other phenotypes (p<0.001). There were no significant differences in patient prognosis between the phenotypes of breast cancer.
CONCLUSIONS
MABC are distinguishable from other phenotypes based on the apocrine histology and a higher expression rate of HER-2.

Keyword

Breast neoplasms; Molecular apocrine; Immunohistochemistry

MeSH Terms

Breast
Breast Neoplasms
Estrogens
Humans
Immunohistochemistry
Keratins
Phenobarbital
Phenotype
Prevalence
Prognosis
Receptor, Epidermal Growth Factor
Receptor, erbB-2
Receptors, Androgen
Estrogens
Keratins
Phenobarbital
Receptor, Epidermal Growth Factor
Receptor, erbB-2
Receptors, Androgen
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