We have had the same problem. We come to the conclusion that it was water 
droplets. We had the problem when our humidity was high in the lab, or our 
weekend run. The changes we made where :
1. We no longer process over the weekend . We cannot count on our heating and 
cooling in our building.
2. We place a towel and a thick piece of cardboard on top of the processor lid.
3.We do not use the really fine mesh cassettes. We will use formalin soaked 
sponges or perm papers.
4. We do not over pack cassette basket.
We had our processor check every time we saw the artifact and they could never 
find a problem with the processor.
Hope this help, Roberta

-----Original Message-----
From: Morken, Timothy [mailto:timothy.mor...@ucsf.edu]
Sent: Wednesday, April 22, 2015 11:16 AM
To: Sue; Lisa Roy
Cc: histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: Nuclear "Artifact"

"One pathologist said it looks like the tissue has been cooked."  Which could 
also be drying artifact after bx, before formalin.

"The only issue is we can have two biopsies right next to one another in the 
basket one looks good and one looks bad. My director also thinks it is the 
processors."

Same processor but two results? Solving intermittent problems takes time to 
check variables - time almost no one wants to spend to check out every 
possibility. But if one variable is the same for both, and the result is 
different, then most likely it is a different variable causing the problem.

I think the other idea suggested of checking the handling of the tissue at the 
source of the biopsy is more likely to shed some light on this issue.


Tim Morken
Pathology Site Manager, Parnassus
Supervisor, Electron Microscopy/Neuromuscular Special Studies Department of 
Pathology UC San Francisco Medical Center





-----Original Message-----
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sue
Sent: Tuesday, April 21, 2015 4:55 PM
To: Lisa Roy
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Nuclear "Artifact"

OMG we are experiencing the same issue. At first it was just GI and now we are 
seeing it on prostate. One pathologist said it looks like the tissue has been 
cooked. The only issue is we can have two biopsies right next to one another in 
the basket one looks good and one looks bad. My director also thinks it is the 
processors. I had Thermo out and they could find nothing. We changed out all 
the reagents and the biopsies were fine than two days later we had some bad 
ones. I know in July Fisher had a formalin recall associated to the mixture of 
buffer, water and formalin. We thought that might be it but it is now almost a 
year later and all the bad formalin should be gone. The histotechs say the 
tissue is crunchy and they are right. I am running a test tonight of a small 
needle biopsy that I made from a colon. I placed it is straight formaldehyde 
overnight and am processing it on our biopsy cycle tonight. My director also 
wanted us to only put three levels on our Thermo, but he wanted the middle 
level to have empty baskets. I stopped that today because I think the other 
issue is that the poor biopsies may be on the top level and as the reagents are 
used the level changes, and also due to displacement with the middle level 
being empty the reagent levels may not reach the top. We just do not have the 
manpower to inspect every reagent every day, we have 6 processor and it would 
take a tech all day. We actually take a digital picture when they come out of 
the processor. I want to check my problems cases tomorrow. We do not use 
sponges but the only other like was the PA who was wrapping the blue paper very 
tight around the tissue. I really do not think this is the issue though.. Any 
other insight would be greatly appreciated.

Susan T. Paturzo
TJUH
_______________________________________________
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
DISCLAIMER: The information in this message is confidential and may be legally 
privileged. It is intended solely for the addressee. Access to this message by 
anyone else is unauthorized. If you are not the intended recipient, any 
disclosure, copying, or distribution of the message, or any action or omission 
taken by you in reliance on it, is prohibited and may be unlawful. Please 
immediately contact the sender if you have received this message in error. 
Thank you.
_______________________________________________
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet

Reply via email to