[Histonet] Breast Lumpectomies..MACRO sections..and prostates
Bernice Frederick
b-frederick <@t> northwestern.edu
Thu Oct 25 11:34:43 CDT 2007
Eric,
Do you have the catalogue numbers for the coverslips and large slides for
the megacassette? We had someone bring us in custom cut slides and getting a
coverslip on them was a joke. We used regular coverslips (4 of them)
Thanks,
Bernice
Bernice Frederick HTL (ASCP)
Northwestern University
Pathology Core Facility
710 N Fairbanks Court
Olson 8-421
Chicago,IL 60611
312-503-3723
-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu
[mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of Gagnon, Eric
Sent: Thursday, October 25, 2007 9:50 AM
To: histonet <@t> lists.utsouthwestern.edu
Subject: [Histonet] Breast Lumpectomies..MACRO sections..and prostates
Robert, we're not currently doing lumpectomies, but we have recently done 32
whole prostate glands and counting, so here's what we're doing in that
regard, as some of the equipment and processes could be useful in your
situation.
We cut on the Leica RM2255 automated microtome. We obtained their Super
Mega Cassette Clamp, (part no 140502 38967). This clamp mounts easily onto
the microtome, and holds SurgiPath SuperCassettes (Cat No VSP59067B-BX grey
in colour). The beauty of this microtome is that the stroke is 10 mm longer
than our previous Reichert-Jung microtomes, I believe it is 70 mm
vertically. In terms of slides, we had some on hand, from Fisher and other
mfgrs, that are 75x38, 75x50, 75x80 mm, with coverslips that are 35x50,
45x50, and 48x65, whatever will hold and cover the tissue, depending on each
specimen. The slides go on our automated stainer, held diagonally with
other slides to keep them vertical, and coverslipped by hand.
In terms of processing for these sections, we use our normal overnight
processing cycle as we would for our routine surgical blocks. These
sections are well-fixed before processing, cut at 4-5 mm during grossing.
Having said that, breast is a whole different ball game than prostate, and
section thickness is going to be more critical, and probably more of a
challenge to achieve, and you might adopt a processing protocol that has
some steps extended, since your specimen won't be as homogeneous as a
prostate gland, i.e. fatty areas, solid/fibrous areas.
It would be interesting to learn about these diagnostic excisional
lumpectomies. Like the prostates, I presume it is to give the pathologist a
better picture of what is going on in a larger area than will fit on a
standard slide?
I should add that I learned a lot about this topic on the Histonet, which
helped a lot in developing our method!
Hope I have been of help in turn. I'd also be interested in opening this
topic up to other organs that are being sectioned elsewhere in a MACRO way.
Eric Gagnon MLT
Histology Laboratory
Kingston General Hospital
Kingston, Ontario, Canada
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