“…Samples of lesions and routine organs were fixed in 10 per cent neutral buffered formalin, processed routinely, sectioned at 3â
ÎŒm and stained with H&E. On select slides, automated dewaxing, rehydration, heat-induced epitope retrieval (PT link, Pre-Treatment Module for Tissue Specimens) and automated incubation (Dako Autostainer Universal Staining System) with anti-human CD3, anti-human CD79a (both Dako Denmark A/S, Glostrup, Denmark) and anti-human CD56 (Clone 123C3, Invitrogen, Paisley, UK) were carried out similar to described in previous investigations (O'Connor and others 2012, Schaffer and others 2012, Ota-Kuroki and others 2013, Sakamoto and others 2013, Ueno and others 2014, Wiggans and others 2014). …”