[Histonet] Derm IHC question
Tony Henwood (SCHN)
tony.henwood at health.nsw.gov.au
Sun Feb 10 16:49:09 CST 2019
Possibly, the edges have been allowed to dry prior to immersion in fixative.
Also is there evidence of cautery artefact?
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA)
Principal Scientist, the Children's Hospital at Westmead
Adjunct Fellow, School of Medicine, University of Western Sydney
Tel: 612 9845 3306
Fax: 612 9845 3318
Pathology Department
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA
-----Original Message-----
From: Debra Siena via Histonet [mailto:histonet at lists.utsouthwestern.edu]
Sent: Saturday, 9 February 2019 3:51 AM
To: 'histonet'
Subject: [Histonet] Derm IHC question
Hello fellow Histonetters
I would like to ask you a question about IHC staining and derm cases. I am seeing a peculiar issue going on, where the melanocytes in the middle of the tissues are staining pretty well but when you get to the ends of the tissues either shaves or ellipses, they are not staining. This is sporadic, not every case and there is no consensus as to a common thread between the cases. I feel that this may be a fixation issue but was just wondering if anyone had ever seen the same phenomena and would be willing to share the theory or even better what was the remedy behind this issue. The fixative is 10% Neutral Buffered Formaliln and the cells in question that are "dropping out" which is what the pathologist is describing are melanocytes, especially with Sox-10 and Mart 1 antibodies.
Thanks for the assistance, I definitely appreciate it very much.
Best wishes,
[image001] Debbie Siena, HT(ASCP)QIHC
Empowering Anatomic Pathology
Technical Support Manager, StatLab
2090 Commerce| McKinney, TX 75069
t: 800.442.3573 ext 229 | m: 469-400-6897 | f: 972-436-1369 dsiena at statlab.com<mailto:dsiena at statlab.com>|www.statlab.com<http://www.statlab.com/>
StatLab is an ISO 13485 Certified Company
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