Primary aldosteronism comprises two different conditions, the tumoral
form usually caused by an adenoma and the idiopathic form due to nodul
ar hyperplasia of the two adenals. More rarely, an adenoma of the adre
nal cortex, glucocorticosteroid-sensitive hyperplasia, and angiotensin
-sensitive adenoma or an autonomous nodule transformed to primary tumo
ral hyperplasia, may be observed. Primary alderosteronism may be conce
ived as a spectrum of genetic abnormalities which express themselves e
ither by hyperplasia or by a tumour. A defect in steroid genesis and p
rolonged stimulation of the cortex would lead to the formation of nodu
les which may become autonomous and generate a tumour. Hypertension ma
y be isolated. Detection requires three sampling of serum potassium in
all hypertensive patients, a study of the aldosterone-renin axis when
the value is less than 3.6 mEq, or whenever the hypertension is sever
e or resistant to treatment. The diagnosis is made by the association
of an increased plasma aldosterone level before getting up in the morn
ing and a plasma renin unaffected by orthostatism. The choice of medic
al or surgical treatment depends on the uni- or bilateral anatomic sub
strate. Computerised tomography, very sensitive but not specific, like
hormonal studies, often provides incomplete answers. Adrenalectomy is
indicated in the presence of a mass of centimetric proportions with c
oncordant results of the dynamic test. In other situations, investigat
ions are continued with the search for an aldosterone gradient by sele
ctive venous sampling. This is very valuable to determine the laterali
sation but fails in 25 % of cases, and its results have to be compared
with those of imaging techniques: CT scan, venography and, when neces
sary, scintigraphy. However, when all investigations have been complet
ed, it is not always possible to reach a definitive conclusion. In non
-surgical patients, in the absence of anatomical proof, the diagnosis
remains presumptive. Progress is awaited in the detection of normokali
emic forms and in the identification of surgically suitable cases whic
h are certainly underestimated,