Normotensive primary hyperaldosteronism is exceedingly rare. We report two
new cases of this syndrome in two middle-aged women, one of Asian origin. T
he presenting signs were tetany in one case and an adrenal mass in the othe
r, Neither patient had hypertension, despite repeated measurements with a m
anual armlet. A typical biological profile of primary hyperaldosteronism wa
s demonstrated in both patients, including hypokalemia with inappropriate k
aliuresis, elevated resting plasma aldosterone, and undetectable plasma ren
in activity. The circadian rhythm of blood pressure was studied by ambulato
ry monitoring pre- and post-operatively. It confirmed the lack of hypertens
ion, but the circadian rhythm of blood pressure was lost before surgery in
one patient. Surgical removal of the histologically typical aldosterone-pro
ducing adenomas normalized the kalemia. The main finding in these two patie
nts was spontaneously low blood pressure in the post-operative period, This
suggests that excess aldosterone induced relative hypertension in these pa
tients whose blood pressure was spontaneously very low. Genetic screening f
or dexamethasone-sensitive hyper aldosteronism was negative in both patient
s.