Neuroendocrine cells associated with neuroendocrine carcinoma of the breast: nature and significance

J Clin Pathol. 2012 Aug;65(8):699-703. doi: 10.1136/jclinpath-2012-200765. Epub 2012 May 3.

Abstract

Background: The developmental mechanisms of breast neuroendocrine carcinoma (B-NEC) have not been sufficiently analysed and are not well understood.

Aims: To investigate NE cells in the background tissues surrounding B-NECs.

Methods: Three cases (four breasts) having many NE cells in the background tissues of multifocal B-NECs were identified at the University of Yamanashi Hospital and St Luke's International Hospital, Japan. These patients were, respectively, 28-, 31- and 38-year-old women with no familial history of NE tumour. The totally-resected breasts were serially studied by immunohistochemistry for specific NE markers (chromogranin A/synaptophysin) and the morphologies and/or localisation of NE cells were investigated.

Results: Immunohistochemical examination showed extensively-distributed NE cells in the background mammary ducts/lobules of the NECs in all breasts. These NE cells were classifiable into three emerging patterns: isolated/scattered, clustered and circumferential. Their distributions were intermingled and were not clearly related to B-NEC foci. NE cells were morphologically polygonal, oval or columnar with sometimes eosinophilic and/or fine-granular cytoplasm and round-to-ovoid nuclei lacking atypia. Some cells were located between epithelial and myoepithelial cells. Apical snouts were occasionally observed in NE cells forming luminal structures.

Conclusions: Benign-appearing NE cells in the parenchyma of a breast with NEC could be regarded as hyperplastic from their emerging patterns and distribution; this NE cell hyperplasia may be associated with the histogenesis of B-NEC as a precancerous condition. These observations might raise questions about the treatment for B-NEC.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers, Tumor / analysis
  • Breast Neoplasms / chemistry
  • Breast Neoplasms / pathology*
  • Breast Neoplasms / surgery
  • Carcinoma, Neuroendocrine / chemistry
  • Carcinoma, Neuroendocrine / pathology*
  • Carcinoma, Neuroendocrine / surgery
  • Cell Shape
  • Chromogranin A / analysis
  • Female
  • Humans
  • Hyperplasia
  • Immunohistochemistry
  • Neuroendocrine Cells / chemistry
  • Neuroendocrine Cells / pathology*
  • Prognosis
  • Synaptophysin
  • Vesicular Transport Proteins / analysis

Substances

  • Biomarkers, Tumor
  • CHGA protein, human
  • Chromogranin A
  • SYP protein, human
  • Synaptophysin
  • Vesicular Transport Proteins