As Greg has already  mentioned, placing control sections on each patient slide 
will assist in troubleshooting your staining issue. Joanne, I don't believe you 
mentioned it in your initial email, but did you attempt a repeat and if so, did 
the results replicate on the repeat? Occasionally there may be a mixing issue 
or other physical issue with the covertile that inhibits complete reaction 
across the slide.

Eric Gagnon MLT
Histology Laboratory
Kingston General Hospital,
Kingston, Ontario, Canada

________________________________________
From: Joanne Clark via Histonet [histonet@lists.utsouthwestern.edu]
Sent: Tuesday, November 29, 2016 4:09 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] ER/PR Uneven Staining

I had a breast needle core today that when stained with ER and PR the staining 
was uneven throughout the core, even though the cancer cells were present in 
the entire core.  The specimen had 10 hours fixation in 10% NBF.  I could 
understand the uneven staining from inadequate fixation on large grossed in 
breast tissue, but 10 hours with  needle core biopsies has always been more 
than sufficient.  Does anyone have any ideas?  We use Leica's ER and PR 
antibodies on the BOND.



Joanne Clark, BAAS, HT(ASCP)CM
Director of Histology

P.   (575) 622-5600
C.   (575) 317-6403
F.   (575) 622-3720
TF. (800) 753-7284

pcnm.com


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