General Features of Malignant Breast Aspirate

 

 

Uploaded: 2007-08-13,  Updated: 2007-08-13

 

 

Malignant Breast Aspirate

Cellularity

Abundant
Patterns Loose, disorderly, dispersed, irregular clusters/glands, many single cells

Cells

Uniform or obvious atypia, single population, increased mitoses

Pleomorphism

May be prominent
Cytoplasm Intracytoplasmic lumens, mucin positivity, lipid vacuoles
Nuclei Usually large (>2RBCs), often eccentric, crowded, lost polarity
Nuclear Membrane Thick, irregular
Chromatin fine to coarse, hyperchromatic, irregular
Nucleoli Often prominent, irregular or multiple
Sentinel Nuclei Usually absent
Background Usually necrotic, cellular smear, nuclear debris, mucin, ghost cells

 

 

Infiltrating Ductal Carcinoma

 

  • Sheets or cords with abundant single tumor cells;

  • Prominent atypia;

  • May have marked stromal fibrosis;

  • Fine to coarse calcification;

  • Mucin positive, especially intracytoplasmic mucin, lipid vacuoles.

Lobular Carcinoma
 
  • Often multicentric and bilateral;
  • Monomorphic, moderate cellularity, with small isolated cells and a few dyshesive small groups;
  • Small angular cells (8-12um) with small to moderate cytoplasm and relatively defined cell borders;
  • Cytoplasmic vacuoles common, intracytoplasmic lumens common;
  • Small round to angular eccentric nuclei with slightly molding and irregular nuclear membrane;
  • Fine to granular chromatin with minimal hyperchromasia and one or two small nucleoli;
  • Sparse or absent naked bipolar nuclei.

Ductal Carcinoma In Situ

 

  • Compared with infiltrating ductal carcinoma, DCIS has less atypical cells, less atypia, less pleomorphism, but has more cohesive, more orderly, more naked bipolar nuclei and more benign component.

Medullary Carcinoma

 

  • Often presents as a soft, round, mobile and well-defined mass in younger patient;

  • Relatively good prognosis;

  • Very cellular, single cells and loose, syncitial aggregates, with no or little gland formation and no mucin;

  • Tumor cells are large, highly pleomorphic. Intact cells have a delicate cytoplasm with indistinct cell borders;

  •  Many naked often distorted tumor cells;

  • Large pleomorphic nuclei with irregular membranes, highly clumped chromatin and prominent nucleoli;

  • May show marked mitoses and necrosis;

  • Prominent lymphocyte and plasma cell infiltration.

Colloid Carcinoma

 

  • Large, well-defined tumor with a soft, jelly-like consistency. Very good prognosis;

  • Islands of tumor cells floating in a mucin pool;

  • Tumor cells often in relatively cohesive sheets, balls or acini;

  • Relatively monotonous and may show deceptively bland;

  • Relatively uniform nuclei in size and shape with fine chromatin and inconspicuous nucleoli;

  • No or rare signet-ring cells;

  • Differential diagnosis: fibroadenoma with mucoid degeneration, benign papilloma, benign mucocele-like lesions and cystic hypersecretory duct carcinomas.

Tubular Carcinoma

 

  • Small tumor, often multicentric and bilateral, good prognosis;

  • Cellular, predominant cohesive clusters with sparse single cells

  • Rigid, angular or twisted tubules with a central core of lumen, and glands with pointed, arrowed outlines;

  • Well-differentiated tumor cells with cytological bland; focal atypia often present;

  • Minimal nuclear enlargement and pleomorphism; often irregular nuclear membrane;

  • Fine chromatin with small nucleoli;

  • Intracytoplasmic lumens present;

  • Sparse or absent naked bipolar nuclei;

  • Differential diagnosis: fibroadenoma, papilloma, fibrocystic changes with hyperplasia, adenosis with radical scar.

Apocrine Carcinoma

 

  • Abundant large malignant apocrine cells; many naked tumor cells;

  • Abundant finely granular cytoplasm;

  • Round to irregular eccentric nuclei with marked atypia;

  • Irregular thick nuclear membrane with coarse irregular chromatin and prominent nucleoli;

  • Large intracytoplasmic hyaline globules;

  • May show prominent necrosis.

 

 

Reference

 
  • The art and science of cytopathology. Richard M Demay, MD. 1996

  Summarized by Zenggang Pan, MD, PhD