Delivering the most effective clinical therapy in acute promyelocytic leuka
emia (APL) is dependent on accurately making the diagnosis. The morphologic
al diagnosis can be improved by detecting the presence of a specific chromo
some translocation, the t(15;17)(q22;q21). This can be achieved using cytog
enetics, RT-PCR, FISH and anti-PML monoclonal antibody. The optimal approac
h will be rapid, accurate and readily integrated into the routine haematolo
gy laboratory. Immunofluorescent detection of microparticulate PML protein
fulfils these criteria, however, karyotyping will also detect the variant t
ranslocations and remains the 'gold-standard'.