[Histonet] IHC Formalin vs frozen
JColCLEFA <@t> aol.com
JColCLEFA <@t> aol.com
Sat Sep 11 17:37:43 CDT 2004
My lab works like most clinical labs in that all tissue is submitted in
fixative for H&E staining first. Once the pathologist sees the H&E sections he or
she will determine whether special stains or Immunostains are required. We
process about 100,000 surgical cases per year, and I do about 400 Immuno slides a
day. It is much easier and more efficient to work with paraffin blocks rather
than cut 400 frozen slides each day for our 5 hour TAT requirement. I've
worked with frozen and paraffin processed material extensively, (I also run our
muscle biopsy lab) and as a muscle tech I assume you realize how labor
intensive it would be to handle such a high volume of varied tissue (bone marrow
biopsies, fatty and fibrous breast tissue, cytology specimens etc) in a frozen
arena. We also recieve breast tissue and colon tumor tissue from other hospitals
and from as far back at 1980 and the standard of care is formalin fixation and
paraffin processing. We have done intensive comparison studies (frozen to
fixed) and I can assure all my pathologists that our staining reactions are
optimal. In our high volume, low staffing (me and 1 other tech) situation, it's
easier to keep as many procedures as similar as possible. Also, lastly, we cut 2
micron sections for 40% of our slides and the distortion from freezing+ the
thinness of section required eliminate the utility of frozen sectioning.
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