Cytologic diagnosis of signet-ring cell carcinoma of the breast

Acta Cytol. 1998 May-Jun;42(3):650-6. doi: 10.1159/000331821.

Abstract

Objective: To examine the cytologic features of signet-ring cell carcinoma (SRCC), defined as carcinoma dominated by signet-ring cells, of the breast and to discuss problems that occur in cytodiagnosis.

Study design: Five cases of SRCC of the breast were examined cytopathologically. Signet-ring cells were subclassified into intracytoplasmic lumina (ICL) type and non-ICL type. ICL type had large ICL containing mucin. Non-ICL-type cells had wide, amorphous cytoplasm diffusely dispersed with mucin.

Results: In cases 1 and 2, fine needle aspiration biopsy (FNAB) revealed many signet-ring cells (non-ICL type), suggesting SRCC. Histologic diagnoses were ductal SRCC containing many signet-ring cells (non-ICL type). In cases 3 and 4, signet-ring cells (ICL type) were found sporadically among carcinoma cells without signet-ring features. Signet-ring cells were not regarded as the major component of the cells; thus, the cytologic diagnoses were lobular carcinoma, not otherwise specified. Pathologic diagnoses were lobular SRCC. Signet-ring cells were mostly ICL type. In case 5, most carcinoma cells on the smears showed signet-ring features (non-ICL type), suggesting SRCC. The histologic diagnosis was lobular SRCC, and signet-ring cells were mostly non-ICL type.

Conclusion: Ductal SRCC yielded more cellular smears as compared with lobular SRCC; therefore, cytologic diagnosis was easier in the former.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Biopsy, Needle
  • Breast Neoplasms / chemistry
  • Breast Neoplasms / diagnosis*
  • Breast Neoplasms / pathology
  • Carcinoma, Ductal, Breast / chemistry
  • Carcinoma, Ductal, Breast / pathology
  • Carcinoma, Lobular / chemistry
  • Carcinoma, Lobular / pathology
  • Carcinoma, Signet Ring Cell / chemistry
  • Carcinoma, Signet Ring Cell / diagnosis*
  • Carcinoma, Signet Ring Cell / pathology
  • Cell Nucleus / ultrastructure
  • Diagnosis, Differential
  • Disease Progression
  • Female
  • Humans
  • Middle Aged
  • Mucins / analysis
  • Neoplasm Invasiveness
  • Neoplasm Proteins / analysis
  • Neoplasms, Multiple Primary / chemistry
  • Neoplasms, Multiple Primary / diagnosis*
  • Neoplasms, Multiple Primary / pathology
  • Prognosis

Substances

  • Mucins
  • Neoplasm Proteins