For the record please note that I have over thirty-six years experience working 
in a Histology lab.   I have been a supervisor or manager  of a hospital and 
clinic histology department for at least 25 years.

Jim Vickroy
Histology Manager
Springfield Clinic, Main Campus, East Building
1025 South 6th Street
Springfield, Illinois  62703
Office:  217-528-7541, Ext. 15121
Email:  jvick...@springfieldclinic.com<mailto:jvick...@springfieldclinic.com>


From: Jamal Rowaihi [mailto:j.rowa...@alborglaboratories.com]
Sent: Tuesday, February 16, 2016 1:56 PM
To: Manfre, Philip; Rene J Buesa; Vickroy, James
Cc: جمال الرويحي; histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Nuclear Bubbling

Great, I agree



Regards

Jamal Rowaihi
Anatomic Pathology Supervisor
Al Borg Medical Laboratories
Sent from my cell phone
-------- Original message --------
From: "Manfre, Philip via Histonet" 
<histonet@lists.utsouthwestern.edu<mailto:histonet@lists.utsouthwestern.edu>>
Date: 2/16/2016 10:44 PM (GMT+03:00)
To: Rene J Buesa <rjbu...@yahoo.com<mailto:rjbu...@yahoo.com>>, "Vickroy, 
James" <jvick...@springfieldclinic.com<mailto:jvick...@springfieldclinic.com>>
Cc: histonet@lists.utsouthwestern.edu<mailto:histonet@lists.utsouthwestern.edu>
Subject: Re: [Histonet] Nuclear Bubbling

Sort of a rude response to someone looking for help.

-----Original Message-----
From: Rene J Buesa via Histonet [mailto:histonet@lists.utsouthwestern.edu]
Sent: Tuesday, February 16, 2016 1:12 PM
To: Vickroy, James; 
histonet@lists.utsouthwestern.edu<mailto:histonet@lists.utsouthwestern.edu>
Subject: Re: [Histonet] Nuclear Bubbling

If I remember correctly, this issue has been discussed previously.The general 
consensus as to the cause of nuclear "bubbling" (in reality a lack of staining 
in the nuclear area) has been attributed to an incomplete section drying.After 
the section has be "fished" from the water bath, if the slide is not set to 
drain the underneath water before drying, the nuclear components are dissolved 
hence when the section is stained, there is nothing to stain → "nuclear 
bubbling".I think this has been previously stated so I really do not understand 
posting this same question again.I do not think that posting again the question 
a different answer is going to be received.rené

    On Tuesday, February 16, 2016 12:32 PM, "Vickroy, James via Histonet" 
<histonet@lists.utsouthwestern.edu<mailto:histonet@lists.utsouthwestern.edu>> 
wrote:



Struggling to find an answer.  We do a lot of GI biopsies in our lab.  
Sometimes they look wonderful without any nuclear bubbling, other times the 
bubbling is pretty intense.  Since nuclear bubbling is often attributed to 
incomplete fixation we of course have investigated the fixation times.  I do 
not find that the problem is fixation.  In fact some of the biopsies end up 
fixing for 48 hrs before processing. (weekend).  There was a suggestion last 
week or so that there might be water trapped under the slides after cutting and 
before staining.  I really thought that this might be the issue however I'm not 
sure at this point.  Extra drying seems to help but sometimes slides side by 
side are so variable, one with bubbles and one without.  I also don't believe 
the problem is in the processing schedule since the problem has shown up on 
both a rapid and a normal schedule. (therefore longer dehydration, clearing, 
etc.)

I am wondering if anyone else has worked with this issue.  Here are my 
questions:


1.        Could it be something that is happening with the tissue before it 
gets to the lab?  Usually a delay if fixation  causes other artifacts but not 
bubbling.  Could it be heat from the GI procedure?

2.      We do use blue sponges for our biopsies.  I know some say get rid of 
the sponges but has anyone seen this problem caused by usage of sponges?

3.      What about the heat stage in our Prisma stainer?


I am really getting frustrated.  Pathologists never complain however I would 
rather all of the tissue did not have the "nuclear bubbling".  Again we only do 
biopsies so I really don't think the standard old " not enough time in 
formalin" is the issue.  I have even wondered about variables such as we use 
recycled formalin, recycled Clearite III.

Any suggestions?

Jim



Jim Vickroy
Histology Manager
Springfield Clinic, Main Campus, East Building
1025 South 6th Street
Springfield, Illinois  62703
Office:  217-528-7541, Ext. 15121
Email:  
jvick...@springfieldclinic.com<mailto:jvick...@springfieldclinic.com<mailto:jvick...@springfieldclinic.com%3cmailto:jvick...@springfieldclinic.com>>



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