“…This is due to the objective difficulty of separating leukemic from nonleukemic conditions [1,10], and to the relative paucity of adequate information on the clinical characters, laboratory features, and evolution of the multifar ious hemopoietic dysplasias [12,22,23]. The interest in these disorders lies both in the necessity for sharper diagnostic criteria, and the shortage of adequate therapy [4,10,22], Moreover, hemopoietic dysplasias pro vide a natural model, in humans, for investigation of a developing leuke mia, or of a disease situated at the boundary of leukemia [1,10,12,22]. The importance of these points was emphasized during a symposium re cently held in Paris, leading to a proposition for an international registry for hemopoietic dysplasias [8].…”