We are having similar issues with our tissue. 
Any troubleshooting insight would be greatly appreciated!
Thanks!

________________________________________
From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Sue 
[suetp...@comcast.net]
Sent: Tuesday, April 21, 2015 7:55 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
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