[Histonet] Protargol S

2014-10-20 Thread Freida Carson
Does anyone have a source for good protargol for Bodian stains? A friend in 
Sweden is asking.

Sent from my iPhone
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] books

2011-06-16 Thread Freida Carson
Thanks to everyone.  The books are sold and now I will have room for something 
else maybe.

Freida Carson
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] Downsizing my library

2011-06-15 Thread Freida Carson
I am downsizing my library and have the following books, mostly out of print, 
for sale.  If you are interested, make an offerf or any of them with enough to 
cover postage also. I hate to just throw them away. Please do this to my 
private email and not on histonet.

Carson:  Histotechnology: A Self-Instructional Text - 2nd edition.
2007
Bancroft and Cook: Manual of Histological Techniques and their Diagnostic 
Application. 1994

Montgomery: Health and Safety Guidelines for the Laboratory, 1995.

Dapson and Dapson: Hazardous Materials in the Histopathology Laboratory. 3rd 
ed, 1995

Wheater, Burkitt and Daniels: Functional Histology. 1987.

Lillie and Fullmer: Histopathologic Technic and Practical Histochemistry. 1976

Kiernan: Histological  Histochemical Methods. 1999.

Vacca: Laboratory Manual of Histochemistry.  1985

Bancroft and Stevens: Theory and Practice of Histological Techniques. 1996


Freida Carson 

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


Re: [Histonet] Re: Chromium Trioxide

2009-07-22 Thread Freida Carson
Bob is correct that there is no satisfactory substitute for chromic acid in the 
GMS procedure.  We found that it takes 1 hour at 56-60 degrees C in 1% periodic 
acid to equal the usual oxidation with chromic acid, and even then you will 
probable get more silver staining of the connective tissue than with chromic 
acid.  The paper was published in the J Histotechnol, 1999; Vol 22:119.
 
If you rinse sections very well with water before the chromic acid, the chromic 
acid can be used for over and over.  It is alcohol remaining on the slides that 
causes the chromic acid to turn brown and become unusuable.
 
Hope this helps.
 
Freida Carson

--- On Wed, 7/22/09, Robert Richmond rsrichm...@gmail.com wrote:


From: Robert Richmond rsrichm...@gmail.com
Subject: [Histonet] Re: Chromium Trioxide
To: histonet@lists.utsouthwestern.edu
Date: Wednesday, July 22, 2009, 2:02 PM


Deanne Knutson, Anatomic Pathology Supervisor, St. Alexius Medical
Center, Bismarck, North Dakota asks:

We use Chromium Trioxide in our GMS stain, and the cost has escalated 
tremendously. Does anyone use a substitute for this chemical?  I am curious 
what others are using for their GMS stain. We still do our stains manually at 
the present time.

There is no completely satisfactory substitute for chromium trioxide
(chromic acid) for the oxidation step for the GMS stain for fungi,
particularly if you're trying to stain Histoplasma. Many kits
substitute periodic acid, usually in inadequate amounts. Freida Carson
published a careful study of this problem several years ago and
concluded that periodic acid could be substituted, with sufficient
time and temperature. (I think I can find this reference, but it's
probably already in our archives.) Last time I looked (2006) the
Ventana method still used chromium trioxide.

Bob Richmond
Samurai Pathologist
Knoxville TN

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


Re: [Histonet] anyone tried to get onto the NSH website today?

2009-07-20 Thread Freida Carson
As of 11:30 CDT the NSH site is up and running or at least I did not have a 
problem getting it to come up.
 
Freida Carson

--- On Mon, 7/20/09, Kim Merriam kmerriam2...@yahoo.com wrote:


From: Kim Merriam kmerriam2...@yahoo.com
Subject: [Histonet] anyone tried to get onto the NSH website today?
To: Histonet histonet@lists.utsouthwestern.edu
Date: Monday, July 20, 2009, 7:46 AM


Good morning everyone,

I have tried several times to get onto the NSH website today and I keep getting 
an error.  I am wondering if it is down or if there is something wrong on my 
end.

Kim
 Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA 



___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


Re: Fw: Re: AW: [Histonet] AFB Recycling Formalin for Fresh Tissue

2009-05-28 Thread Freida Carson
Wang reported on the contamination of tissue sections with AFB by the use of 
fluorescence microscopy, and if I remember correctly, when he tested the water 
in water fountains, he found something like 33% contained AFB.  Non-pathogenic, 
but we can't tell that on our stains. The paper is in Am J Clin Pathol 51:71, 
1969.  We (Carson, Kingsley, Haberman, and Race) also reported the 
contamination in the 1964 issue of the same journal.  We stopped using tap 
water for our water baths and began using millipore filtered water that had 
already been through a deionizing column and charcoal filter.  We always cut a 
negative control from the same days workload as the patient case - uterus in 
our case.  You don't need a positive control cut the same day, just a positive 
control with only a medium number of organisms.  We also did not use any tap 
water in the deparaffinization prior to the carbol fuchsin.  AFB organisms have 
also been reported growing in 40
 gal formalin tanks believe it or not and in the old Fisher Paraffin wafers.
 
We centrifuged tap water in 50-ml tubes, poured off the supernatent, and 
refilled and recentrifuged until we could see some sediment in the bottom.  We 
took that to Microbioloby and had it cultured to definited prove the presence 
of AFB in the tap water.
I would recommend this approach to anyone suspecting tissue contamination. 
 
Freida Carson
--- On Thu, 5/28/09, Akemi Allison-Tacha akemiat3...@yahoo.com wrote:


From: Akemi Allison-Tacha akemiat3...@yahoo.com
Subject: Fw: Re: AW: [Histonet] AFB  Recycling Formalin for Fresh Tissue
To: Histonet Histonet@lists.utsouthwestern.edu
Date: Thursday, May 28, 2009, 1:21 PM


Hello,
I responded to Gudrun personally, but I thought that the information I am 
supplying him below might be a good educational source for other histologists 
who are having similar scenario's for AFB contamination.  

I would also like to say that I have an extremely eager histology team that 
have expressed an interest in learning theory and practice.  Most of my team 
are OJT.  They have had several pathologists approach them with these concerns 
regarding AFB, and because of their knowledge, or lack of it, couldn't fix the 
problem.  We are starting with the basics and I am giving in-services along the 
way.

Hi  Gudrun,

They are shipping the recycled formalin directly to the outside hospital 
surgery to put their fresh tissues into.

As far as the AFB, we have had intermitant (+) AFB on the edges of tissues, 
that has been extremely questionable.  We currently are not cutting a negative 
(-)  positive(+) control on the same water bath as the test sample. That will 
be remedied beginning Monday. The water here is also in question.  I will be 
sending it out for microbacteria analysis.

We are going through a thorough housekeeping and in-service process.  We are 
starting with the tissue processors, which are currently only changed weekly 
(not rotated daily), embedding centers, which have to my knowledge, never been 
drained, and the hopper cleaned-out.  The water baths are not scrubbed out with 
soap and HOT water daily and
covered at night to prevent contamination.  The water bath is not skimmed of 
excess tissue debris, each and every time another specimen is placed on it.  
The Carbol Fuchsin is not being filtered prior to use.  The working solution is 
currently being poured back into the stock bottle.  Need I go on

Akemi Allison-Tacha BS, HT (ASCP) HTL
Histology Manager
Associated Pathology Medical Group Laboratories
105A Cooper Ct. Los Gatos, CA 95032
Cell: 425.941.4287 
W: E-Mail: aallison-ta...@apmglab.com
P: E-Mail: akemiat3...@yahoo.com



--- On Thu, 5/28/09, Gudrun Lang gu.l...@gmx.at wrote:

From: Gudrun Lang gu.l...@gmx.at
Subject: AW: [Histonet] Recycling Formalin for Fresh Tissue
To: akemiat3...@yahoo.com
Cc:
histonet@lists.utsouthwestern.edu
Date: Thursday, May 28, 2009, 10:34 AM

Just for interest. Your lab takes the recycled formalin to make 4% neutral
buffered formalin (NBF)? Or do they ship the recycled formalin directly in
bottles to the surgery?
AFB = acid fast bacili?

Do you have concerns, that they produce false-positive AFB stains? I cannot
imagine, that a (hopefully) small number of dead bacili on the surface of
tissue will pretend this. An other question: Isn't there a filter in the
recycler to prevent such contamination?
Gudrun

-Ursprüngliche Nachricht-
Von: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] Im Auftrag von
akemiat3...@yahoo.com
Gesendet: Donnerstag, 28. Mai 2009 18:14
An: Histonet
Betreff: [Histonet] Recycling Formalin for Fresh Tissue

Good Morning Histo Land,

I am asking all you out there to give me your input on recycIing formalin. 
I realize this has been discussed in the not too distant past, but this may
be a little different situation.  I realize some labs are recycling formalin
to put on their tissue processors