There is no known immunosuppressive therapy for autoimmune premature ovaria
n failure that has been proven safe and effective by prospective randomized
placebo-controlled study. Nevertheless, immunosuppression using corticoste
roids has been used on an empirical basis for this condition. Here we prese
nt two cases of young women with premature ovarian failure who were treated
with glucocorticoids in the hopes of restoring fertility. The first case i
llustrates the potential benefit of such therapy, and the second case illus
trates a potential risk. The first patient with histologically proven autoi
mmune oophoritis was treated with alternate day glucocorticoid treatment. S
he had return of menstrual bleeding six times and ovulatory progesterone co
ncentrations four times over a 16 week period. The second patient with pres
umed but unconfirmed autoimmune ovarian failure was referred to us after ha
ving been treated with a 9 month course of corticosteroids. During that tre
atment her menses did not resume. The corticosteroid treatment was complica
ted by iatrogenic Gushing syndrome and osteonecrosis of the knee. Identifyi
ng patients with autoimmune premature ovarian failure presents the opportun
ity to restore ovarian function by treating these patients with the proper
immune medullation therapy. On the other hand, potent immune medullation th
erapy can have major complications. Corticosteroid therapy for autoimmune p
remature ovarian failure should be limited to use in placebo-controlled tri
als designed to evaluate the safety and efficacy of such treatment.