essage-
> From: Terri Braud via Histonet histonet@lists.utsouthwestern.edu
> Sent: Monday, October 28, 2019 10:14 AM
> To: 'histonet@lists.utsouthwestern.edu' histonet@lists.utsouthwestern.edu
> Subject: Re: [Histonet] Cell block processing
>
> [External Email] This ema
Terri Braud via Histonet
Sent: Monday, October 28, 2019 10:14 AM
To: 'histonet@lists.utsouthwestern.edu'
Subject: Re: [Histonet] Cell block processing
[External Email] This email originated from outside of the organization. Think
before you click: Don’t click on links, open atta
We collect our FNAs in CytoLyt. We also use it to wash all our non-gyn fluids,
but then we fix the cell block "pellet" in formalin.
We have had no problems with immunos, and are able to lyse the RBCs to provide
a nice, clear specimen.
Hope this helps.
Terri L. Braud, HT(ASCP)
Anatomic Pathology
tmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA
From: Charles Riley via Histonet
Sent: Friday, 25 October 2019 23:12
To: Histo List
Subject: [Histonet] Cell block processing
Does anyone have any ti
ober 25, 2019 12:57 PM
To: Joe W. Walker, Jr.
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Cell block processing
[External Email] This email originated from outside of the organization. Think
before you click: Don’t click on links, open attachments or respond to requests
;reserved=0>
-Original Message-
From: Charles Riley via Histonet
mailto:histonet@lists.utsouthwestern.edu>>
Sent: Friday, October 25, 2019 8:13 AM
To: Histo List
mailto:histonet@lists.utsouthwestern.edu>>
Subject: [Histonet] Cell block processing
[External Email]
t; joewal...@rrmc.org, www.rrmc.org
>
> -Original Message-
> From: Charles Riley via Histonet
> Sent: Friday, October 25, 2019 8:13 AM
> To: Histo List
> Subject: [Histonet] Cell block processing
>
> [External Email] This email originated from outside of the organizat
: [Histonet] Cell block processing
[External Email] This email originated from outside of the organization. Think
before you click: Don’t click on links, open attachments or respond to requests
for sensitive information if the email looks suspicious or you don’t recognize
the sender.
Does
Does anyone have any tips or suggestions on how to better process extremely
bloody FNA specimens?Is there anyway to clear out some or all of the
blood without destroying the other tissues?
--
Charles Riley BS HT, HTL(ASCP)CM
Histopathology Coordinator/ Mohs
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