“…The malignant cells have in particular the surface, cytochemical and biochemical features of immature thymocytes (Kaplan et al, 1974;Gatien et al, 1975;Coccia et al, 1976;Jaffe et al, 1976;Stein et al, 1976;Donlon et al, 1977;Stein & Muller-Hermelink, 1977;Kersey et al, 1978;Kung et al, 1978;Lukes et al, 1978a, b;Bollum, 1979;Long et al, 1979). The marked propensity for progression to leukaemia establishes a continuum between these tumours and a subset of acute lymphoblastic leukaemia (ALL), i.e., the 25% of cases of ALL with T-cell markers (Kersey et al, 1973;Sen & Borella, 1975;Tsukimoto et al, 1976 (Catovsky et al, 1974). In our series of lymphoblastic lymphomas, cases which did not form E rosettes tended to manifest AP activity as a diffuse multigranular reaction.…”