Processing fetal brain tissue
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From: | JMeade0710@aol.com |
To: | histonet@pathology.swmed.edu |
Reply-To: | |
Content-Type: | text/plain; charset="US-ASCII" |
Fellow netters:
I have a real problem, looking for a solution (no pun intended).
We process approximately 100 fetal autopsies per year, and most of them
contain extensive neuro studies.
My laboratory is part of a large system and standardization is the
current buzz word. We are attempting to standardize most processes and
procedures.
During our processing cycles on the VIP, we are not getting adequate
stiffening of this very difficult tissue. It constantly wants to crumble and
fragment.
We employ zinc formalin fixation, and fix for several days before
sectioning takes place. And allow the sections to remain in fresh fix an
additional 24 hours after the gross is taken.
My question and hopefully your solutions focus on what can we do to
attain improved processing, so the embedding process is more successful and
our sections appear better for our pathologist.
At one juncture the lab employed CBA formalin, and the resultant sections
were better, but under our standardization process, we cannot use the CBA
formalin any longer.
You thoughts and remarks are most welcome.
Jerry Meade
Detroit Medical Center
University Laboratories
Hutzel Hospital
Detroit, Mi.
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