[Histonet] Cryostats

2008-11-24 Thread LYork
Can anyone provide information on portable cryostats?  We need one that
will handle only 4-5 frozens per week.  

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Re: [Histonet] RE: Floaters

2008-11-24 Thread Histonet Alias
ANP.23350 Phase II
N/A   YES   NO



*Are flotation baths clean and well-maintained, and is there a procedure for
preventing cross-contamination of paraffin sections in the bath?*

* *

NOTE:  Of particular importance are periodic water changes or blotting of
the water surface so that sections from one patient block are not
inadvertently carried over to another case (so-called floaters or
extraneous tissue).



COMMENTARY:

On Mon, Nov 24, 2008 at 4:44 AM, Edwards, R.E. [EMAIL PROTECTED] wrote:

 I tend to  try and  poke them down with a metal coat hanger!.

 -Original Message-
 From: [EMAIL PROTECTED] [mailto:
 [EMAIL PROTECTED] On Behalf Of
 [EMAIL PROTECTED]
 Sent: 21 November 2008 18:17
 To: [EMAIL PROTECTED]
 Subject: [Histonet] Floaters

 Would anyone care to share their policy on floaters? Also, does anyone
 know if there is a CAP policy in floaters?

 Teresa Hallada BS, MT/CT (ASCP)
 Lead Cytotechnologist
 MidMichigan Health - Gratiot
 [EMAIL PROTECTED]
 989.463.1101 ext 3423

 Please note that this email message and any attachments may contain
 privileged and confidential information that is protected against use or
 disclosure under federal and state law.  The information is intended only
 for the personal and confidential use of the intended recipient. If the
 reader of this message is not the intended recipient or the employee or
 agent responsible for delivering it to the intended recipient, you are
 hereby notified that you have received this information in error and that
 any review, dissemination, distribution, copying or action taken in reliance
 on the contents of this communication is strictly prohibited.  If you have
 received this email in error, please advise by immediate reply.
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RE: [Histonet] RE: Floaters

2008-11-24 Thread Robyn Vazquez
Rope and a cinder block??!!  Happy Monday!

-Original Message-
From: [EMAIL PROTECTED] [mailto:[EMAIL PROTECTED] On Behalf Of Histonet Alias
Sent: Monday, November 24, 2008 6:09 AM
To: Edwards, R.E.
Cc: [EMAIL PROTECTED]; [EMAIL PROTECTED]
Subject: Re: [Histonet] RE: Floaters

ANP.23350 Phase II
N/A   YES   NO



*Are flotation baths clean and well-maintained, and is there a procedure for
preventing cross-contamination of paraffin sections in the bath?*

* *

NOTE:  Of particular importance are periodic water changes or blotting of
the water surface so that sections from one patient block are not
inadvertently carried over to another case (so-called floaters or
extraneous tissue).



COMMENTARY:

On Mon, Nov 24, 2008 at 4:44 AM, Edwards, R.E. [EMAIL PROTECTED] wrote:

 I tend to  try and  poke them down with a metal coat hanger!.

 -Original Message-
 From: [EMAIL PROTECTED] [mailto:
 [EMAIL PROTECTED] On Behalf Of
 [EMAIL PROTECTED]
 Sent: 21 November 2008 18:17
 To: [EMAIL PROTECTED]
 Subject: [Histonet] Floaters

 Would anyone care to share their policy on floaters? Also, does anyone
 know if there is a CAP policy in floaters?

 Teresa Hallada BS, MT/CT (ASCP)
 Lead Cytotechnologist
 MidMichigan Health - Gratiot
 [EMAIL PROTECTED]
 989.463.1101 ext 3423

 Please note that this email message and any attachments may contain
 privileged and confidential information that is protected against use or
 disclosure under federal and state law.  The information is intended only
 for the personal and confidential use of the intended recipient. If the
 reader of this message is not the intended recipient or the employee or
 agent responsible for delivering it to the intended recipient, you are
 hereby notified that you have received this information in error and that
 any review, dissemination, distribution, copying or action taken in reliance
 on the contents of this communication is strictly prohibited.  If you have
 received this email in error, please advise by immediate reply.
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[Histonet] RELIA Histology Careers Bulletin for 11-30 and A Few Holiday Shopping Tips!!

2008-11-24 Thread Pam Barker
Hi Histonetters!

I hope you are having a wonderful Fall.  The weather is getting cooler
and the Holidays are right around the corner. 

 

I realize that at this time of year a job change is the furthest thing
from most people’s minds but I have some great opportunities that I
wanted to share along with some great tips for holiday shopping.

 

All of my positions are full time permanent positions with premier
companies who offer excellent salaries, benefits and relocation
assistance.  Most of them are willing to look at onsite interviews and
start dates after the holidays so if you or anyone you know might be
looking now or after the first of the year it wouldn’t hurt to shoot me
a quick e-mail at  mailto:[EMAIL PROTECTED] [EMAIL PROTECTED]
or give me a quick call toll free at 866-607-3542.

 

Currently I have management positions in CA, NH, OH and TX.  I also have
tech positions in CA, TX, WA, MD and MA.

 

Holiday shopping is always fun, crazy, chaotic, inspiring, and
challenging.  Here are some tips that might save you some time, money
and stress.

Black Friday is the day after Thanksgiving the official first day of
Holiday Shopping.  If you want a heads up on the advertisements from
your favorite stores go to the website:

 http://www.bfads.net/ www.bfads.net  They have a lot of the ads
posted on their site NOW that will be in your newspaper on Thanksgiving
morning.

The Monday after Thanksgiving is known as Cyber Monday it is the busiest
online shopping day of the year and there is another website that will
give you heads up on deals for Cyber Monday.  This website is
http://www.cybermonday.com/ www.cybermonday.com  The best part of this
site is that the stores that advertise on their site donate a percentage
of sales to a scholarship fund.

 

Again if you or anyone you know is interested in a new opportunity now
or after the holidays get in touch with me.  There are a lot of
recruiters out there but remember I am the only one with the experience,
connections and respect for you and your career that specializes
exclusively in histology.  I want to place you in a new position only if
it is the right place, right time and right position for you.  And I am
always available for career advice, resume assistance or just a chat.
Let me be your career advocate.  

 

Happy Holidays!!!

Pam

866-607-3542

 mailto:[EMAIL PROTECTED] [EMAIL PROTECTED]  

 

Thank You! 

 

Pam Barker
President
RELIA 
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:  mailto:[EMAIL PROTECTED] [EMAIL PROTECTED] 
mailto:[EMAIL PROTECTED] mailto:[EMAIL PROTECTED]
 http://home.earthlink.net/~relia1
http://home.earthlink.net/~relia1
 http://www.myspace.com/pamatrelia www.myspace.com/pamatrelia 
http://www.myspace.com/pamatrelia http://www.myspace.com/pamatrelia

 

 

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[Histonet] Career Opening: Histology Manager with leading lab in Dallas, TX

2008-11-24 Thread CareerStudio
Currently a Histology Manager role is open with a leading, full-service 
clinical reference laboratory in Dallas, TX.  Reporting to the Laboratory 
Director, 
accountabilities will include:

- Management of all technical and operational activities of the Histology 
Department, including staffing, planning, coordination and evaluation 
- Troubleshooting quality and production issues including stains, processes, 
systems, and equipment.
- Developing and implementing improvements in systems and processes for 
enhanced efficiency and quality, while managing growth.

8+ years of experience in histology with at least 5 years of supervisory 
experience is required for this position, with demonstrated management ability, 
organizational and training skills.  Must have HT (ASCP) certification, minimum 
of Associates degree, excellent written and oral communication skills, as well 
as Microsoft Office and database management background.

Our client is offering attractive base salary commensurate with experience, 
and relocation assistance is available.

We are a part of a national search firm focused on the laboratory and 
biotechnology sectors.  Our clients nationwide are premier laboratories with 
the 
latest in equipment and teams of valued professionals.

Please contact Barbara Siegel at [EMAIL PROTECTED] if you are interested 
in an opportunity in this fine city.

Career Studio
national search
Palm Beach, FL
[EMAIL PROTECTED]
561-738-6363



**
One site has it all. Your email accounts, your social networks, 
and the things you love. Try the new AOL.com 
today!(http://pr.atwola.com/promoclk/10075x1212962939x1200825291/aol?redir=http://www.aol.com/?optin=new-dp
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RE: [Histonet] Leica slide writer - problems??

2008-11-24 Thread Stephen.Eyres
Hi Joyce,

Was this a recent problem, and has it been resolved? 

Thanks

Steve 

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Joyce
Cline
Sent: Thursday, November 20, 2008 6:20 PM
To: Histonet
Subject: RE: [Histonet] Leica slide writer - problems??

We have had the same problems, we discovered the slide surface on some
of the snowcoat slides changed to a slick surface instead of a rough
surface. 
We have switched to a pale gray slide that still has the rough surface
and we have not had any printing wipe off.

Joyce Cline, H.T. (ASCP)
Technical Specialist
Hagerstown Medical Lab.
301-665-4980
fax 301-665-4941


-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of
[EMAIL PROTECTED]
Sent: Thursday, November 20, 2008 7:16 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Leica slide writer - problems??

Hi,
 
Has anyone else been having problems with there Lieca slide writer. Our
problems mainly involve the ink writing rubbing off before and after
staining!!, we use Surgipath snowcoated slides, what does everyone else
use as they have hinted it could be our slides. Any help would be
fantastic.
 
Thanks Loads
 
Sara 
 
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[Histonet] Iron stains

2008-11-24 Thread Tom McNemar
We may be having a problem with our iron stains.  I say that we 'may' be having 
a problem because our positive control always works.  

For bone marrows, we stain the core, aspirate, a smear, and a purchased 
positive control.  The stain is all over the place.  We may have a loaded smear 
with a negative core and aspirate.  We may have a positive aspirate with a 
negative core and smear.  We may have all negatives even though clinically, 
there should be iron.  Our control always works.  The pathologists do not trust 
the stain and really do not believe the results.  I have stood by the stain due 
to the positive control but I find it increasingly difficult.

I would appreciate any thoughts.  Our procedures are outlined below...

The aspirate is allowed to clot before placing it into 10%NBF.
The core is placed briefly into DecalStat (until it floats) then placed 
into 10%NBF.
Both are then processed with our regular tissues.  The spend anywhere 
from 4 to 10 hours in formalin.
The following day, they are cut and along with one of the purchased 
controls, run down to water on the stainer.  (8 mins onboard
oven, americlear, alcohols, water)
The smear is placed into 95% alcohol then rinsed in distilled.
All slides are then stained using Perl's Method for iron pigment.

We have already explored the way the specimens are collected during the BM 
procedure, and decal solution.  All reagents are good.  I'm wondering about the 
formalin fixation.  I know that threre are other probably better fixatives.  
Does anybody use another fixative prior to formalin?  For those using formalin 
only, do you limit the fixation time in any way?

I really would appreciate any comments.  Such a common and simple stain.  We 
should be able to trust it.  

Thanks.

Tom McNemar, HT(ASCP)
Histology Co-ordinator
Licking Memorial Health Systems
(740) 348-4163
(740) 348-4166
[EMAIL PROTECTED]
www.LMHealth.org


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RE: [Histonet] Iron stains

2008-11-24 Thread Weems, Joyce
I would always fix first before decal. The acid is stripping the iron.
After discontinuing B5 fixative, we use B-Plus (zinc), but some are very
happy with 10% NBF. The problem with purchased controls is that they are
not treated the same as your material, but at least you know your
reagents are good!

My 2 cents... J:)

Joyce Weems
Pathology Manager
Saint Joseph's Hospital 
5665 Peachtree Dunwoody Rd NE
Atlanta, GA 30342
Please note new phone and fax numbers
678-843-7376 - Phone
678-843-7831 - Fax



-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Tom
McNemar
Sent: Monday, November 24, 2008 12:07 PM
To: [EMAIL PROTECTED]
Subject: [Histonet] Iron stains

We may be having a problem with our iron stains.  I say that we 'may' be
having a problem because our positive control always works.  

For bone marrows, we stain the core, aspirate, a smear, and a purchased
positive control.  The stain is all over the place.  We may have a
loaded smear with a negative core and aspirate.  We may have a positive
aspirate with a negative core and smear.  We may have all negatives even
though clinically, there should be iron.  Our control always works.  The
pathologists do not trust the stain and really do not believe the
results.  I have stood by the stain due to the positive control but I
find it increasingly difficult.

I would appreciate any thoughts.  Our procedures are outlined below...

The aspirate is allowed to clot before placing it into 10%NBF.
The core is placed briefly into DecalStat (until it floats) then
placed into 10%NBF.
Both are then processed with our regular tissues.  The spend
anywhere from 4 to 10 hours in formalin.
The following day, they are cut and along with one of the
purchased controls, run down to water on the stainer.  (8 mins onboard
oven, americlear, alcohols, water)
The smear is placed into 95% alcohol then rinsed in distilled.
All slides are then stained using Perl's Method for iron
pigment.

We have already explored the way the specimens are collected during the
BM procedure, and decal solution.  All reagents are good.  I'm wondering
about the formalin fixation.  I know that threre are other probably
better fixatives.  Does anybody use another fixative prior to formalin?
For those using formalin only, do you limit the fixation time in any
way?

I really would appreciate any comments.  Such a common and simple stain.
We should be able to trust it.  

Thanks.

Tom McNemar, HT(ASCP)
Histology Co-ordinator
Licking Memorial Health Systems
(740) 348-4163
(740) 348-4166
[EMAIL PROTECTED]
www.LMHealth.org


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[Histonet] Dissolve plastic

2008-11-24 Thread Lee Peggy Wenk


I Need Histonetters help.
 
We have an eye with a plastic part for the lens, which is a type of
telescope, I've been told.
 
According to the new pathologist, we need to dissolve out this plastic lens,
then he can gross the eye and we can process it into paraffin.
 
We've never had to dissolve plastic before. The eye is in 10% NBF right now.
I'm guess maybe something like chloroform? But what percent? For how long?
Before or after grossing?
 
Has anyone done this before, that can send a procedure to me? Thanks.
 
 
***

Peggy A. Wenk, HTL(ASCP)SLS
Program Director,  Schools of Histotechnology
Supervisor, Mortuary Services
Laboratory Safety Officer, Disaster Preparedness and Quality Assurance
Coordinator
Department of Anatomic Pathology, 100RO
William Beaumont Hospital
3601 W. 13 Mile Road
Royal Oak, MI 48073-6769
Work   248/898-9079
Fax  248/898-9054
E-mail  [EMAIL PROTECTED]
Web Page: http://www.beaumont.edu/alliedhealth 


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[Histonet] Peggy - eye/plastic lens

2008-11-24 Thread Vicki Kalscheur
Hi Peggy:  It is possible that acetone ( swab on, or soak) will dissolve or 
loosen the lens without cellular damage. I have not done this and will be 
interested to see what other suggestions are made.  Vicki
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[Histonet] Re: Floaters

2008-11-24 Thread Robert Richmond
Teresa Hallada in Michigan asks: Would anyone care to share their
policy on floaters? Also, does anyone know if there is a CAP policy
[on] floaters?

At Gastonia we sent 'em on to the state ME's office - they had an
adequately ventilated autopsy suite

But seriously, folks, I've never heard of any regulatory agency having
a policy on floaters - extraneous tissue on a slide that's floated in
from some other case.

What I was taught in residency - sometime in the late Ordovician
period, I think it was - not to mention them in a report, but write
floater on the slide before filing it.

I've never heard anybody observe this, but there are two kinds of
floaters: individual tissue sections (the responsibility of the
microtomist) and whole chunks of tissue (the responsibility of whoever
grossed the specimen). Since the trouble-shooting for these two
problems is entirely different, you first have to determine which kind
of floater you've got. Obviously if it's a whole chunk of tissue,
you'll get repeated sections of it.

If it's whole chunks of tissue, then the grosser isn't cleaning
instruments adequately between cases. If I ran the zoo, I'd have
several sets of instruments, throw them in a pot as I used them, and
wash them when I ran out of instruments, but the Hospital
Administrator's Official Handy-Dandy Book on How to Make Life Hard for
the Anatomic Pathology Service specifies that there be only one set of
grossing instruments in the lab at a time.

(I've never actually seen this book, but I'm absolutely sure it exists.)

Bob Richmond
Samurai Pathologist
Knoxville TN

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Re: [Histonet] immuno set-up

2008-11-24 Thread Dana Settembre
I agree with Mr. Brooks on the Shandon Sequenza - fantastic for low
volume.


Dana Settembre, HT ASCP
Immunohistochemistry Lab
UMDNJ - University Hospital
Newark, NJUSA


 Amos Brooks [EMAIL PROTECTED] 11/21/08 4:58 PM 
Hi,
   For small volumes like that, check with Thermo. They have various
sizes
of IHC stainers that have different slide capacities. Alternatively
you
could check out the Shandon Sequenza. I could find more info if you
are
interested. (BTW: I have no Thermo ties.)

Amos Brooks


Message: 19
Date: Thu, 20 Nov 2008 20:21:21 +
From: [EMAIL PROTECTED] 
Subject: [Histonet] immuno set-up
To: histonet@lists.utsouthwestern.edu 
Message-ID:
   
[EMAIL PROTECTED]



Content-Type: text/plain

Hello all,

I work at a private lab with one pathologist, and one histotech (me).
We do
about 5,000 cases a year. We are intrested in doing our immuno's in
house
(right now we send them out), and wanted to know your opinion on the
type of
equipment that would be best for this situation. Right now we send
about 5
to 10 cases a week out for immuno's.

All responses are very much appreciated

Jenny
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[Histonet] Error question

2008-11-24 Thread Jesus Ellin
Was wanting to know how people handle accession errors within the
pathology information system,, to elaborate on this, is when a person
receives in the specimen with a requisition and they have to do data
entry into the system.  What is allowable?, what is the percent error
rate?, how are people dealing with errors?  How are you dealing with
personnel??  This is becoming an issue and I wanted to survey people out
there how they are handling this issue,? Any help would greatly be
appreciated.

 

 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

* Office:  (928) 336-1743

*Fax:  (928) 336-7319

*Email: [EMAIL PROTECTED] 

 




This message is confidential, intended only for the named 
recipient(s) and may contain information that is privileged 
or exempt from disclosure under applicable law.  If you are 
not the intended recipient(s), you are notified that the 
dissemination, distribution, or copying of this message is 
strictly prohibited.  If you receive this message in error, 
or are not the named recipient(s), please notify the sender 
at either the e-mail, fax, address, or telephone number 
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[Histonet] as Thanksgiving approaches, what do you think about a gall bladder in vinegar ?

2008-11-24 Thread Della Speranza, Vinnie
I have a patient requesting her gall bladder be returned to her for religious 
reasons.
The premise I've been given is so that, upon death, the patient may be stored 
with her body parts.

My facility has concerns about providing it to her in formalin (for obvious 
reasons) or alcohol. The patient admits this is a family practice with momma's 
appendix already being stored in the attic.

It can get a bit toasty warm here in the South so attic storage of a specimen 
in alcohol may not be prudent and I can't be absolutely certain it wouldn't 
burn the house down, another potential liability for my institution.

I'm tempted to give it to her in food grade vinegar, to avoid the potential 
liabilities from using anything that could be considered hazardous.
Assuming that returning her gall bladder is a given, what do you think of using 
vinegar for this purpose?



Vinnie Della Speranza

Manager for Anatomic Pathology Services

Medical University of South Carolina

165 Ashley Avenue  Suite 309

Charleston, South Carolina 29425

Tel: (843) 792-6353

Fax: (843) 792-8974

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RE: [Histonet] as Thanksgiving approaches, what do you think about a gall bladder in vinegar ?

2008-11-24 Thread Weems, Joyce
Could you give it to her in a plastic bag, with a container, and tell
her to store it in rubbing alcohol? j

Joyce Weems
Pathology Manager
Saint Joseph's Hospital 
5665 Peachtree Dunwoody Rd NE
Atlanta, GA 30342
Please note new phone and fax numbers
678-843-7376 - Phone
678-843-7831 - Fax

 

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Della
Speranza, Vinnie
Sent: Monday, November 24, 2008 5:37 PM
To: histonet
Subject: [Histonet] as Thanksgiving approaches, what do you think about
a gall bladder in vinegar ?

I have a patient requesting her gall bladder be returned to her for
religious reasons.
The premise I've been given is so that, upon death, the patient may be
stored with her body parts.

My facility has concerns about providing it to her in formalin (for
obvious reasons) or alcohol. The patient admits this is a family
practice with momma's appendix already being stored in the attic.

It can get a bit toasty warm here in the South so attic storage of a
specimen in alcohol may not be prudent and I can't be absolutely certain
it wouldn't burn the house down, another potential liability for my
institution.

I'm tempted to give it to her in food grade vinegar, to avoid the
potential liabilities from using anything that could be considered
hazardous.
Assuming that returning her gall bladder is a given, what do you think
of using vinegar for this purpose?



Vinnie Della Speranza

Manager for Anatomic Pathology Services

Medical University of South Carolina

165 Ashley Avenue  Suite 309

Charleston, South Carolina 29425

Tel: (843) 792-6353

Fax: (843) 792-8974

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Re: [Histonet] Dissolve plastic

2008-11-24 Thread Joseph Saby
Lee and Peggy-

We section these eyes all the time with the plastic in place.  

I would certainly suggest a gluaraldehyde fixative.  Straight NBF is a very 
poor fixative for the many tissues found in eyes, especially the retina.  If 
you contact me directly, we can talk off line.  Eyes have held a special 
fascination with me for many years.

Joe Saby
NAMSA





From: Lee  Peggy Wenk [EMAIL PROTECTED]
To: histonet@lists.utsouthwestern.edu
Sent: Monday, November 24, 2008 12:47:24 PM
Subject: [Histonet] Dissolve plastic



I Need Histonetters help.

We have an eye with a plastic part for the lens, which is a type of
telescope, I've been told.

According to the new pathologist, we need to dissolve out this plastic lens,
then he can gross the eye and we can process it into paraffin.

We've never had to dissolve plastic before. The eye is in 10% NBF right now.
I'm guess maybe something like chloroform? But what percent? For how long?
Before or after grossing?

Has anyone done this before, that can send a procedure to me? Thanks.


***

Peggy A. Wenk, HTL(ASCP)SLS
Program Director,  Schools of Histotechnology
Supervisor, Mortuary Services
Laboratory Safety Officer, Disaster Preparedness and Quality Assurance
Coordinator
Department of Anatomic Pathology, 100RO
William Beaumont Hospital
3601 W. 13 Mile Road
Royal Oak, MI 48073-6769
Work  248/898-9079
Fax      248/898-9054
E-mail  [EMAIL PROTECTED]
Web Page: http://www.beaumont.edu/alliedhealth 


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RE: [Histonet] as Thanksgiving approaches, what do you think about a gall bladder in vinegar ?

2008-11-24 Thread joelle weaver

You know, I really think that the vinegar is a great idea! I can't think of any 
reason off-hand why it would be hazardous, flammable, toxic, or bring on any 
liability. Even the isopropyl can be flammable, and if you told her to use it, 
you might be somewhat at fault ( though I know a bit of a stretch). In any 
case, I think that I'll try to remember that in case I encounter any similar 
requests...
 
Thanks
Joelle Date: Mon, 24 Nov 2008 17:40:38 -0500 From: [EMAIL PROTECTED] To: 
[EMAIL PROTECTED]; histonet@lists.utsouthwestern.edu Subject: RE: [Histonet] 
as Thanksgiving approaches, what do you think about a gall bladder in vinegar 
? CC:   Could you give it to her in a plastic bag, with a container, and 
tell her to store it in rubbing alcohol? j  Joyce Weems Pathology Manager 
Saint Joseph's Hospital  5665 Peachtree Dunwoody Rd NE Atlanta, GA 30342 
Please note new phone and fax numbers 678-843-7376 - Phone 678-843-7831 - 
Fax-Original Message- From: [EMAIL PROTECTED] [mailto:[EMAIL 
PROTECTED] On Behalf Of Della Speranza, Vinnie Sent: Monday, November 24, 
2008 5:37 PM To: histonet Subject: [Histonet] as Thanksgiving approaches, 
what do you think about a gall bladder in vinegar ?  I have a patient 
requesting her gall bladder be returned to her for religious reasons. The 
premise I've been given is so that, upon death, the patient may be stored with 
her body parts.  My facility has concerns about providing it to her in 
formalin (for obvious reasons) or alcohol. The patient admits this is a 
family practice with momma's appendix already being stored in the attic.  It 
can get a bit toasty warm here in the South so attic storage of a specimen in 
alcohol may not be prudent and I can't be absolutely certain it wouldn't burn 
the house down, another potential liability for my institution.  I'm tempted 
to give it to her in food grade vinegar, to avoid the potential liabilities 
from using anything that could be considered hazardous. Assuming that 
returning her gall bladder is a given, what do you think of using vinegar for 
this purpose?Vinnie Della Speranza  Manager for Anatomic Pathology 
Services  Medical University of South Carolina  165 Ashley Avenue Suite 
309  Charleston, South Carolina 29425  Tel: (843) 792-6353  Fax: (843) 
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[Histonet] Warthin-Starry // Best before dates

2008-11-24 Thread V . Neubert

Hello!

I use the Warthin-Starry technique to stain spirochaetes in FFPE sections.

I don't know how long I can keep the AgNO_3 solutions and the hydrochinone 
solution whitout getting them to expire.
Is there anyone who already had to deal with that question?

Regards,

Valentin


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