[Histonet] Re: Stain for HP

2012-10-19 Thread Bob Richmond
Staining gastric biopsy specimens for Helicobacter pylori: practice
varies greatly in various labs I've worked in. One lab does a blue
stain (generic equivalent of Diff-Quik II), while the other does
immunohistochemistry, each of them on all specimens. I've also seen
labs that did a full tissue Giemsa, and one that did a cresyl echt
violet stain. Haven't seen a routine Warthin-Starry in many years. I
think everyone bills every one of these stains they do.

There are still a few hold-outs for real men can see 'em on the H  E.

As far as I know, no studies have been done comparing the sensitivity
(we'll forget specificity) of the various methods. My personal opinion
is that none of the dye or silver methods is conspicuously better than
the others. Reading the blue stain is time-consuming; I use oil
immersion magnification (which real men disdain) to confirm all
positives (and confirm Helicobacter heilmannii, which I have seen
once), and on all apparent negatives with acute inflammation. The IHC
can be read rapidly with much less magnification.

I note that many pathologists sign out any bacteria they see in a blue
stain as Helicobacter, including the frequent bugs that get carried
down from the oral cavity as the scope advances. These pathologists
should definitely switch to IHC.

So if I have one gastric biopsy case a day, I'm happy with the blue
stain. If I have ten, I want IHC. If there is no inflammation, I can
do without any stain.

Bob Richmond
Samurai Pathologist
Maryville TN

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RE: [Histonet] Re: Stain for HP

2012-10-19 Thread Ian R Bernard
Also Alcian Yellow

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bob Richmond
Sent: Friday, October 19, 2012 5:01 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Stain for HP

Staining gastric biopsy specimens for Helicobacter pylori: practice varies 
greatly in various labs I've worked in. One lab does a blue stain (generic 
equivalent of Diff-Quik II), while the other does immunohistochemistry, each of 
them on all specimens. I've also seen labs that did a full tissue Giemsa, and 
one that did a cresyl echt violet stain. Haven't seen a routine Warthin-Starry 
in many years. I think everyone bills every one of these stains they do.

There are still a few hold-outs for real men can see 'em on the H  E.

As far as I know, no studies have been done comparing the sensitivity (we'll 
forget specificity) of the various methods. My personal opinion is that none of 
the dye or silver methods is conspicuously better than the others. Reading the 
blue stain is time-consuming; I use oil immersion magnification (which real men 
disdain) to confirm all positives (and confirm Helicobacter heilmannii, which I 
have seen once), and on all apparent negatives with acute inflammation. The IHC 
can be read rapidly with much less magnification.

I note that many pathologists sign out any bacteria they see in a blue stain as 
Helicobacter, including the frequent bugs that get carried down from the oral 
cavity as the scope advances. These pathologists should definitely switch to 
IHC.

So if I have one gastric biopsy case a day, I'm happy with the blue stain. If I 
have ten, I want IHC. If there is no inflammation, I can do without any stain.

Bob Richmond
Samurai Pathologist
Maryville TN

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[Histonet] RE: labeling pre-made slides

2012-10-19 Thread Hutton, Allison
Thank you for all the suggestions, I now have a few ideas of how to correct 
this.


-Original Message-
From: Goins, Tresa [mailto:tgo...@mt.gov]
Sent: Thursday, October 18, 2012 4:27 PM
To: Hutton, Allison; histonet@lists.utsouthwestern.edu
Subject: RE: labeling pre-made slides


I don't know if you tried these markers specifically, but we have seen 
variation in quality.  We changed vendors because we began having problems with 
our original source - the vendor changed their supplier and tried selling the 
pen as the same as - it was not even close.  

Also, you may try cleaning the frosted area with acetone before labeling.

Tresa

-Original Message-
From: Hutton, Allison [mailto:ahut...@dh.org] 
Sent: Thursday, October 18, 2012 1:39 PM
To: Goins, Tresa; histonet@lists.utsouthwestern.edu
Subject: RE: labeling pre-made slides

Some further clarification...
*We manually coverslip
*We have tried the markers upon reciept but have trouble with them staying on 
due to the spray fixative ending up on the frosted end as well.

-Original Message-
From: Goins, Tresa [mailto:tgo...@mt.gov]
Sent: Thursday, October 18, 2012 3:08 PM
To: Hutton, Allison; histonet@lists.utsouthwestern.edu
Subject: RE: labeling pre-made slides


We have no label maker - so the slides are labeled with a Securline Marker II 
from EMS - stays put through all treatments.
Prior to delivery, a paper label is printed and affixed to the slide over the 
hand-written label.

Tresa 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Hutton, Allison
Sent: Thursday, October 18, 2012 12:27 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] labeling pre-made slides

We use the Leica IPS to label our cytology slides, however, we do get quite a 
few slides from doctors who make smears and spray fix them before they come to 
us.  Unfortunately, they use pencil to label and this usually wipes off during 
staining and coverslipping.  Does anyone else receives slides like this and 
then how are they permanently labeled?  We would like to avoid going back to 
paper labels if at all possible.
Any advice or suggestion is appreciated
Thanks
Allison
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[Histonet] RELIA Histology Careers Bulletin 10/19/2012 TGIF and a beautiful Fall weekend to look forward to!

2012-10-19 Thread Pam Barker
Hi Histonetters!!
TGIF

How are you?  Are you enjoying the sights, sounds and flavors of Fall?
I know I am enjoying college football after all I am a southern gal and you
know how we southerners are about our Football Saturdays in the South.  On
the other hand I am still patiently waiting for that “real Fall stuff”.  You
know like crisp cool air, beautiful fall colors, crunching leaves and
steaming bowls of soup. 

 What are you enjoying most of all about this season?

I also wanted to tell you about some new job opportunities and a new feature
in my career bulletin.
The new feature is:  The Spotlight Job
I will be spotlighting a particular position and providing details in the
email.  To qualify for the spotlight the position has to be beyond the scope
of a regular histology job so you might not see one every time.  These are
the one in a million opportunities!!

Today’s SpotlightJob:
Lead Histology Tech/Supervisor – Growing State of the Art Lab in Topeka, KS
My client is a growing state of the art pathology lab located in Topeka KS.
They are looking for someone with at least 2-3 years of histology experience
and some supervisory experience as well. ASCP HT or HTL is required.   You
will have the opportunity to work with all types of tissue, grossing and ihc
(if you need training it will be provided),  You will also have the
opportunity to learn and use digital pathology.  My client offers a great
salary 100% paid benefits for employees, relocation assistance and a bonus
program.  

I have a number of other really great opportunities For ASCP certified or
eligible histologists:
• Charlotte, NC – Hospital based all shifts available HT/HTL required
• Charlotte, NC – Private Lab Grossing Histotech Afternoon shift HT/HTL
CLIA qual to gross
• Nashville, TN – Private Path Lab Afternoon shift  ASCP HT/HTL or eligible
• Collegeville, PA New Lab – Day shift HT/HTL and CLIA qual to gross
• Reading, PA – In Office Path Lab - Dermpath Histotech Day Shift  HT/HTL
and CLIA qual to gross
• Dallas, TX – Private Reference Lab – IHC Tech ASCP HT/HTL, QIHC preferred.
• Portland, ME – Private Reference Lab – Histotech ASCP HT/HTL or eligible
• Topeka, KS – Lead Histotech/Supervisor – see spotlight job for details.  

If you are interested in participating in my referral program  in addition
to histotechs for these positions I also need cytotechs in TN and SD.

If you or anyone you know might be interested in any of these opportunities
or would like help with a job search in another area of the USA please
contact me.  I can be reached at rel...@earthlink.net or toll free at
866-607-3542.



Thank You!
  
 
Pam Barker
President/Senior Recruiting Specialist-Histology
RELIA Solutions
Specialists in Allied Healthcare Recruiting
5703 Red Bug Lake Road #330
Winter Springs, FL 32708-4969
Phone: (407)657-2027
Cell: (407)353-5070
FAX: (407)678-2788
E-mail: rel...@earthlink.net 
www.facebook.com/PamBarkerRELIA
www.linkedin.com/in/reliasolutions
www.twitter.com/pamatrelia 



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Re: [Histonet] CD31 for FFPE Immunohistochemistry on Mouse Model

2012-10-19 Thread nancy lowen



From: Amy Porter port...@msu.edu
To: 'Histonet' histonet@lists.utsouthwestern.edu 
Sent: Thursday, October 18, 2012 12:35 PM
Subject: [Histonet] CD31 for FFPE Immunohistochemistry on Mouse Model

Anyone out there have CD31 working well on FFPE samples for Mouse Samples??
I know this might be a long shot, however I haven't looked for anything on
this in quite awhile.



Amy S. Porter, HT(ASCP) QIHC

Michigan State University

Investigative HistoPathology Laboratory

William S. Spielman, Ph.D. - Director

Patricia K. Senagore, M.D. - Consulting Pathologist

Department of Physiology / Human Pathology

Biomedical Physical Sciences Building 

567 Wilson Road - Room 2133

East Lansing, MI  48824-3320

Phone:  517-884-5026

Fax:  517-432-1368

port...@msu.edu

http://www.humanpathology.msu.edu/



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I use The antibody from Biocare Medical, and I also purchase the Kit that is 
designed for this antibody.
Works well, even on bone.
Nancy Lowen
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[Histonet] CD31 for FFPE IHC on Mouse

2012-10-19 Thread Mark Elliott
Amy
Can you please share the responses you got with the rest of us
Thanks
Mark
 

Message: 8
Date: Thu, 18 Oct 2012 16:21:55 -0400
From: Amy Porter port...@msu.edu
Subject: RE: [Histonet] CD31 for FFPE Immunohistochemistry on Mouse
Model
To: 'Amy Porter' port...@msu.edu,'Histonet'
histonet@lists.utsouthwestern.edu
Message-ID: 003101cdad6e$3792fc80$a6b8f580$@edu
Content-Type: text/plain;charset=US-ASCII

Thanks to all for responses..looks like most roads lead to once place
which is spectacular!!  Just what I needed.  Amy

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Amy Porter
Sent: Thursday, October 18, 2012 3:36 PM
To: 'Histonet'
Subject: [Histonet] CD31 for FFPE Immunohistochemistry on Mouse Model

Anyone out there have CD31 working well on FFPE samples for Mouse Samples??
I know this might be a long shot, however I haven't looked for anything on
this in quite awhile.



Amy S. Porter, HT(ASCP) QIHC

Michigan State University

Investigative HistoPathology Laboratory

William S. Spielman, Ph.D. - Director

Patricia K. Senagore, M.D. - Consulting Pathologist

Department of Physiology / Human Pathology

Biomedical Physical Sciences Building 

567 Wilson Road - Room 2133

East Lansing, MI  48824-3320

Phone:  517-884-5026

Fax:  517-432-1368

port...@msu.edu

www.humanpathology.msu.edu




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[Histonet] FW: processing after Bouin's fixation

2012-10-19 Thread Rae Staskiewicz
Sending this for a friend, please do not reply to me.

 

  _  

From: Burton, Lynn [mailto:lynn.bur...@illinois.gov] 
Sent: Thursday, October 18, 2012 8:43 AM
To: raest...@grics.net
Subject: FW: processing after Bouin's fixation

 

Rae,

I have been trying to get this out on Histonet and I can't seem to address
it correctly. It is for Dr. Dybas. Would you please help me?

Lynn

 

From: Burton, Lynn 
Sent: Wednesday, October 17, 2012 3:14 PM
To: 'histo...@lists.utsouthwester.edu';
'histonet-boun...@lists.utsouthwestern.edu'
Subject: FW: processing after Bouin's fixation

 

 

 

From: Burton, Lynn 
Sent: Wednesday, October 17, 2012 1:46 PM
To: 'on behalf of Lynn Burton'
Subject: processing after Bouin's fixation

 

Hi,

I have a question about the step in between Bouin's fixation and alcohol
dehydration of rat brain tissue, nucleus accumbans. Several procedures are
suggested by various resources, what are any of you using successfully?

Lynn Burton

Animal Disease Lab

Galesburg,Il

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