Thames Valley Cytology Society

Volume 5 Issue 1
January 2002

 

Architecture of Cervical Cytology

Report by Katie Thunder - Watford General Hospital

 

On the 28th June, 2001, at St Bartholomew's Hospital, Dr Robin Moseley gave an interesting, if not controversial, talk regarding the importance of architecture in cervical ctyology and the potential loss of architecture with the introduction of liquid based cytology.

Dr Moseley began by highlighting two immunolgical markers MIB-1 and E-cadherin that can be useful in distinguishing difficult areas e.g. differentiating between a post-menopausal cervix and CIN 3.

The main features of diagnosis can be split into two areas

  1. cytonuclear features (abnormal chromatin)
  2. architectural features (irregular structure)

These characteristics vary depending on the differentiation of the tumour. With a well-differentiated tumour architectural features are relied upon rather than cytonuclear changes (chromatin appears normal, but can have malignant architecture), whereas with a poorly differentiated squamous cell carcinoma,cytonuclear features are relied upon.

Liquid-based cytology and its implications!

Dr Moseley shared his concerns over the eagerness to readily accept and introduce this fairly new technique straight into the cervical screening programme. This view was backed by his experience of the liquid-based preparations and the noticeable loss of architectural features associated with them.

Conventional Smear
LBC Preparations
Background Some features of background remain
Cytonuclear features Cytonuclear features are the most important factor

Architectural features:
- dispersed single cells
- cell aggregates
- cohort effect
- 3D characteristics

Architectural features:
- cell aggregates
- overall loss of architecture

LBC claims to:

  1. reduce inadequates; imporve preservation; improve representativeness (the preparation is representative of the whole sample). However, LBC material will eventually be thrown away also.
  2. increase sensitivity in detection of CIN 3 (but small, single abnormal nuclei may be difficult to identify and therefore are easily missed).
  3. facilitation of HPV testing (HPV can also be carried out on conventional preparations)
  4. more rapid screening (questionable, cells closer together may cause fatigue on the eyes)
  5. facilitate automation.

In conclusion, he hoped (as do we all in the field of cytology) that the powers that be will wait until they are confident with the LBC preparation before rolling it out nationally and take into account the importance of architecture and the potential implications of losing this diagnostic feature.