Hey Joe,

All the specimens come to the lab fresh.  Instead of the Cytospin collection 
fluid we have been using thin prep preservcyt solution to resuspend, which is 
mostly methyl alcohol.  Do you think that would have some influence to the 
washing problem.  We are staining with the PAP stain.  Thanks for your input 
let me know if you have anymore suggestions.  Nina
________________________________________
From: Joe W. Walker, Jr. <jwwal...@rrmc.org>
Sent: Thursday, November 2, 2017 12:03 PM
To: Nina J. Rich; histonet@lists.utsouthwestern.edu
Subject: RE: cytospin prep

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Hi Nina,

How are the cytology specimens collected?  This will play a role in how you 
process them for evaluation on the Cytospin machine.  We do not utilize the 
mega funnels.  However, cytology specimens should be centrifuge first to remove 
any supernatant.  Then equal parts of the Cytospin collection fluid should be 
added to the cell button and the cell button should be resuspended.  Once 
resuspended, the amount of specimen that you put into the mega funnel chamber 
will vary depending on the cellularity of the cytology specimen.  Large cell 
buttons might require less while small buttons will require more.  If you over 
load the chamber, you will experience the cell spot/square falling off the 
slide when staining.  This assumes that you are Pap staining your slides, hence 
the use of the Cytospin collection fluid.  If you are making airdried specimens 
for Romanowsky stains, if you over load the chamber, you will have the same 
result of the spot falling of the slide.  The manufacturer should provide max 
volume limits for the mega funnels but again a very cellular specimen will 
create issues.  This has been our experience with cytospins.

Joe W. Walker, Jr. MS, SCT(ASCP)
Anatomical Pathology Manager
Rutland Regional Medical Center
160 Allen Street, Rutland, VT 05701
P 802.747.1790  F 802.747.6525
joewal...@rrmc.org, www.rrmc.org
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-----Original Message-----
From: Nina J. Rich via Histonet [mailto:histonet@lists.utsouthwestern.edu]
Sent: Thursday, November 02, 2017 11:38 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] cytospin prep

Good morning,


For all those that have to do cytology cytospins.  We are using the cytospin 4 
with the large square mega funnels.  We have a problem with the specimen always 
washing off the slide.  Is there anyone who can send me their processing 
procedure for this type of funnel, to include whether or not you centrifuge the 
specimen first. The small circular funnels do not wash.  Any input would 
greatly be appreciated.  Jean


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