Thames Valley Cytology Society

Volume 5 Issue 2
June 2002

 

Spring Tutorial - University College Hospital 2002

Report by Ann Mitchell, Stoke Mandeville Hospital

 

The breast was the subject of this years Spring Tutorial. The lectures were held in the newly appointed seminar rooms opposite to the north cloisters UCH. Dr Grace McKee gave a very informative talk about FNA cytology of breast carcinoma: the diagnostic pointers and pitfalls.
It was emphasised that FNA aspiration cytology is an important, quick, reliable diagnostic procedure. Good sampling, preparation and staining are also essential. Typing and grading should be attempted on all carcinomas, though not on scanty or poorly preserved samples.

The abnormal aspirate may contain:

  • increased cellularity.
  • 3D clusters and single malignant cells.
  • enlarged nuclei, can also have in benign aspirates.
  • irregular nuclear margins never in benign, except in liquid based cytology.
  • abnormal chromatin pattern (granular not a sign)
  • abnormal mitoses (not on its own a feature).

Details of one of the many excellent examples shown by Dr McKee included a lobular carcinoma.

  • Intracytoplasmic vacuoles frequently seen but also present in some ductal carcinomas.
  • The vacuoles may produce a signet-ring appearance.
  • The cells are smaller (RBC size).
  • Nuclei may be round to oval but often irregular (in LBC nucleoli become prominent).

Pitfall: Aspirates often scanty and under diagnosed. Cells may be single or in clusters if a large in situ component is present.

Conclusion: FNA aspiration cytology still has a role to play in breast disease. Cytological material useful for marker studies for ER, PR and also HER-2/neu status. Immunocytochemistry, and fluorescence in situ hybridisation can be used. Air-dried smears are good for these studies. Cell blocks can also be prepared with needle rinse material.

Dr Clive Wells gave a good overview of the breast screening programme and the multidisciplinary team involved in the process. There is still a lack of pathologists willing to attend FNA clinics. These clinics are good as the results are rapid and can re-assure patients. Core biopsies have become popular.

A guide for when to use FNA vs. Core was given

FNA Cytology:

  • cysts
  • nipple discharge
  • diffuse thickening
  • lesion difficult position
  • small lymph nodes
  • Pagets

Core Biopsy:

  • stellate lesions
  • low grade micro calcification
  • radiological indeterminate lesions
  • diffuse lobular carcinoma
  • post radiotherapy

Conclusion: There is a need for quality as there are increased expectations of the public. The quality of diagnosis has driven audits into these areas and has therefore improved the service.

 

Professor Lakhani gave an interesting talk on how our present pathology knowledge can be utilised for future molecular work. The methods currently under study are DNA microarray analysis and proteonomics.

Transcriptional profiling can be done using microarrays. Many small tissue sections can be put onto a microscope slide (1,000 specimens). Reference and tumour RNA, labelled with fluorescent dyes, can be hybridised using a probe to the microarray. The slides are scanned with a laser and the intensity of the dyes can be calculated. This can then provide information on under or over expression of genes. The databases then set up can provide profiles of estrogen receptor (ER) status. An example would be for ER negative tumours where the treatment is not so good as for ER positive tumours. The aim was to identify these molecules and use as therapeutic targets.
There are however limitations as with all scientific work. Professor Lakhani concluded by saying that pathologists in the future will need to work closely with molecular analysis.

The afternoon workshops were packed with many interesting cases. This years Spring tutorial was most informative and well organised. Lunch was also very enjoyable and good reason to circulate amongst the delegates.