[Histonet] need ur help
Kim.Donadio <@t> bhcpns.org
Kim.Donadio <@t> bhcpns.org
Tue Dec 21 10:09:52 CST 2010
Thought I did.
Thanks for making sure.
Kim Donadio
Pathology Supervisor
Baptist Hospital
1000 W Moreno St.
Pensacola FL 32501
Phone (850) 469-7718
Fax (850) 434-4996
Tony Henwood <AnthonyH <@t> chw.edu.au>
12/20/2010 04:14 PM
To
"'Kim.Donadio <@t> bhcpns.org'" <Kim.Donadio <@t> bhcpns.org>
cc
"'w_alkadhumi <@t> yahoo.com'" <w_alkadhumi <@t> yahoo.com>,
"histonet <@t> lists.utsouthwestern.edu" <histonet <@t> lists.utsouthwestern.edu>
Subject
RE: [Histonet] need ur help
Kim,
Did you send this to Histonet & Wassan?
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager & Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA
From: Kim.Donadio <@t> bhcpns.org [mailto:Kim.Donadio <@t> bhcpns.org]
Sent: Tuesday, 21 December 2010 9:00 AM
To: Tony Henwood
Subject: RE: [Histonet] need ur help
Are the tiny biopsies freezing after you put them in paraffin? I have
noticed that when you use freeze spray( in your case, maybe the coldness?)
and the paraffin cracks it also cracks the tissue and you can see it
microscopically.
Just a thought.
Kim Donadio
Pathology Supervisor
Baptist Hospital
1000 W Moreno St.
Pensacola FL 32501
Phone (850) 469-7718
Fax (850) 434-4996
Tony Henwood <AnthonyH <@t> chw.edu.au>
Sent by: histonet-bounces <@t> lists.utsouthwestern.edu
12/20/2010 03:30 PM
To
"'wassan alkadhumi'" <w_alkadhumi <@t> yahoo.com>, "
histonet <@t> lists.utsouthwestern.edu" <histonet <@t> lists.utsouthwestern.edu>
cc
Subject
RE: [Histonet] need ur help
Check the fixative the biopsies are going into. Is it 10% neutral buffered
formalin?
Are they being fixed for long enough? Remember these are usually small,
thin biopsies so they do not need extended processing so use the time to
extend the fixation. You could try placing the biopsies in fixative in a
warm oven (37-45oC) before loading onto the processor.
Are they being allowed to dry before being placed in fixative?
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager & Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA
-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu
[mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of wassan
alkadhumi
Sent: Tuesday, 21 December 2010 4:43 AM
To: histonet <@t> lists.utsouthwestern.edu
Subject: [Histonet] need ur help
Hi all
Hope u r all doing well, am an Iraqi histotech working in both
histopathology and IHC department in Iraq. One part of what i do is IHC
(manual) i have no problem with, the other part is what i have problems
with, Renals and Livers, we do regular H &E stain , PAS and Masson
Tirchrome and all of them were text book quality until ten days ago, the
problem is the Stains even the H&E are not Fine, its smugish. And the most
important stain for the histopathologist is the Trichrome which it should
be fine and delacate and its not. I checked the procedures and stain
preparations and i doing it the correctly , I made new solutions and did
prolonged deparaffinization 10 min each step (3 xylenes, 2 100%ETOH, one
90%ETOH, one 70%ETOH) and there was no difference. I should mention that
those problems happened with only Renal and Liver biopsies the H&E and PAS
on other types of tissues are working just great. the one thing that
changed before 10 days ago is the wether it became really cold and our lab
temp. is not controlled. Am going crazy please help me Thank u a lot
Wassan
Histotech.
Shorsh hospital
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