mal range; 30-159) pg/ml and 10 (4.4-17.4) µg/dl, respectively. Although her plasma renin activity (PRA) and ACTH was suppressed to an undetectable level, no further examination was conducted or followedup. One year later, hypertension and progressive edema in the lower extremities gradually appeared. Reexamination revealed hypopotassemia and elevation of plasma aldosterone level as high as 216 (normal range; 30-159) pg/ml, with low PRA as 0.3 (0.5-2.0) ng/ml/ hr. Magnetic resonance imaging demonstrated that the right adrenal mass did not enlarge. Abstract. Synchronous associations of Cushing's syndrome (CS) and primary aldosteronism (PA) with multiple adrenocortical adenomas secreting each hormone independently have rarely been reported. Herein, we describe a unique case of PA associated with CS with detailed clinical and pathological investigations. bilateral adrenal masses with clinical symptoms of CS and PA were found in a 43-year-old woman. Venous sampling demonstrated excess secretion of cortisol, and aldosterone from right, and left tumor, respectively. A bilateral laparoscopic partial adrenalectomy was undergone. The right adrenal tumor (3 cm) was yellow in color with abundant lipofuscin granules, and was composed of both eosinophilic compact cells and clear cells. In situ hybridization showed that both mRNAs for HSd3b2 and CYP17A1 were strongly expressed in the tumor, suggesting cortisol synthesis. Left adrenal tumor (2.4 cm) was golden-yellow in color, and composed of clear cells only. expression of HSd3b2 and CYP11b mRNAs were observed in the tumor compatible with the aldosterone synthesis. Furthermore, minute nodules were found at the surface of normal-appearing cortex on both sides of the adrenal glands, and the expression of HSd3b2 and CYP11b mRNAs was clearly demonstrated within the nodules, indicating aldosterone synthesis. we diagnosed that the present case had 1) cortisol-producing right adrenocortical adenoma, 2) aldosterone producing left adrenocortical adenoma, and 3) cortical minute nodules with aldosterone production in both adrenal glands compatible with idiopathic adrenal hyperplasia. we reviewed the cases reported, and discussed the significance of the minute nodules in the adrenal cortex, often found in association with the adrenocortical adenoma.Key words: Adrenal gland, Cushing's syndrome, primary aldosteronism, bilateral adrenocortical adenomas, Laparoscopic adrenalectomy (Endocrine Journal 56: [495][496][497][498][499][500][501][502] 2009) A JApAnese woman was admitted to a local hospital for the treatment of her depression when she was age 35. Right adrenal mass of less than 20 mm was demonstrated by imaging studies during her workup. At this time, both plasma aldosterone and plasma cortisol levels were within normal limits, at 72 (nor-