“…These facts suggested that hypopituitarism was not present or was partially, if any, before the attack. It has been well recognised that a permanent or transient hypopituitarism including DI may occur with pituitary apoplexy (Brougham eI al., 1950;Taylor et al, 1968;Epstein t al., 1971;Jacobi et al, 1974) and that in some cases of acromegaly and ForbesAlbright syndrome (Forbes et al, 1954), the regression of the disease was observed after apoplexy (Taylor et al, 1968;McLaren et al, 1973;Jacobi et al, 1974). However, it has scarecely been reported that systematic evaluations of the pituitary Vol.25,No.3 PITUITARY APOPLEXY function using synthetic hypothalamic hormones, TRH and LHRH, and direct measurements of several trophic hormones were performed successively during the spontaneous recovery course.…”