[Histonet] GMS Question

Tony Henwood (SCHN) tony.henwood at health.nsw.gov.au
Fri May 1 15:51:07 CDT 2015


I would strongly suggest that you not use Periodic acid for the GMS, its alright for the PAS but for the GMS. Use chromic acid as described the standard texts.
Regards
Tony Henwood MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA)
Laboratory Manager & Senior Scientist, the Children’s Hospital at Westmead
Adjunct Fellow, School of Medicine, University of Western Sydney
Tel: 612 9845 3306
Fax: 612 9845 3318
Pathology Department
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA 
 
________________________________________
From: Paula Lucas [plucas at biopath.org]
Sent: Saturday, 2 May 2015 12:16 AM
To: histonet at lists.utsouthwestern.edu
Subject: [Histonet] GMS Question

Hello,



I think I already know the answer but I'm not sure why so if someone can
help me understand the theory behind it, I would greatly appreciate it.



Currently, we use the Richard Allen kit for the GMS stain and it uses
Periodic Acid as the 1st step.

We use a control tissue from a case we had that was positive for fungus and
it's a fungus ball from the Rt Maxillary.

We ran a test for fungus on a different and current case of the same tissue
(different patient): Rt Maxillary sinus.



The control tissue did work, but the patient's tissue did not, so the doctor
ordered a PAS for fungus and this clearly showed the fungal elements nicely.




My question is why would the control and patient tissue have different
results when they are both fungus balls from the same specimen source?



Thanks in advance,

Paula

Lab Manager

Bio-Path Medical Group

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