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 _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
