Frozen Sections and Intraoperative Consultation
Theatre sends a fresh, visibly fatty sentinel lymph node, 18 by 12 mm, from a 54-year-old woman having breast cancer surgery, for frozen section while she is under anaesthesia. Your cryostat reads minus 14 degrees C and the first sections crumble and smear. The request form mentions tuberculous lymphadenitis treated two years ago. The pathologist expects a slide within 20 minutes. How would you handle this specimen?
What the panel is testing: Whether you can produce a diagnostic frozen section from fatty tissue quickly while protecting staff from unfixed, possibly infectious tissue, and know which decisions are the pathologist's.
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Knowledge: Fat does not freeze firmly at the temperatures that suit most tissues: lymph node cuts well at about minus 15 to minus 20 degrees C, but fatty tissue usually needs minus 25 degrees C or colder, so crumbling and smearing mean the block is too warm. I confirm two identifiers against the request before cutting, because a frozen section result changes the operation in real time. Unfixed tissue from a patient with past tuberculosis is a biosafety risk: cryostat cutting creates aerosols and fragments, and freezing does not kill mycobacteria. The pathologist may choose to trim the fat, cut only the node or use touch imprints. Frozen section has known false negatives, and permanent sections remain the final diagnosis.
Management: Immediately I would tell the pathologist about the tuberculosis history, so the choice between sections and imprints is theirs, and wear gloves, gown, eye protection and the respiratory protection policy requires. I would bring the block colder with the heat extractor or freezing spray, mount it on a pre-cooled chuck, and use a fresh blade with the anti-roll plate set correctly. I would cut sections of about 5 to 8 microns onto labelled slides, fix them at once and run a rapid H&E. After two failed attempts I would call the pathologist to the cryostat rather than keep theatre waiting. The residual tissue goes into formalin, labelled, for permanent sections. Afterwards I would decontaminate the cryostat as contaminated, following the manufacturer and policy, before any other specimen is cut.
Ethics and communication: If the container and form did not match, I would stop. The result goes to the surgeon only through the pathologist, never as my own impression. Any glove tear or exposure is reported to occupational health and through the incident system. The easily missed infection history is a learning point for theatre, raised without blame.
Likely panel follow-up questions
- What cryostat temperature would you use for fatty breast tissue compared with liver?
- Why does freezing not make this specimen safe to handle?
- The pathologist asks for imprints instead. How do you prepare and stain them?
- How do you decontaminate the cryostat after this case?
- What happens to the residual frozen tissue?
Pitfalls in this case
- Cutting before confirming the specimen identity against the request
- Ignoring the infection history or cutting without protective equipment
- Re-cutting repeatedly at the wrong temperature while theatre waits
- Telling the surgeon a diagnosis yourself
- Discarding the residual tissue instead of fixing it for permanent sections
Reference: Bancroft's Theory and Practice of Histological Techniques (8th ed); WHO Laboratory Biosafety Manual, 4th edition (2020)