Non-cushingoid Cushing's syndrome due to adrenocorticotropic hormone-independent bilateral adrenocortical macronodular hyperplasia.

This case report describes a 68-year-old man with Cushing's syndrome due to adrenocorticotropic hormone (ACTH)-independent bilateral adrenocortical macronodular hyperplasia (AIMAH). He was referred to our hospital for evaluation of bilateral enlargement of the adrenal glands found incidentally by computed tomography (CT). He had a ten-year history of hypertension. Although he was normokalemic and did not show Cushingoid features, the diagnosis of ACTH-independent Cushing's syndrome was established by endocrinological examinations. His plasma cortisol showed no diurnal rhythm and was unsuppressible by high-dose (8 mg/day) dexamethasone. Plasma ACTH was undetectable and did not respond to corticotropin-releasing hormone. Excised adrenal glands were markedly enlarged (right 28 g and left 64 g). Macroscopic appearance of the glands showed multiple yellowish nodules typical for AIMAH; microscopic findings were also compatible with AIMAH. The present case indicates that patients with AIMAH sometimes do not show typical Cushingoid features and therefore AIMAH can be found incidentally from ultrasound or CT examination of the abdomen.

[1]  C. Crouzel,et al.  Late sympathetic reinnervation and normalization of canine myocardial beta-adrenergic receptor density following denervation. , 1995, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[2]  F. De Geeter Clinically silent adrenal masses. , 1995, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[3]  S. Koizumi,et al.  Adrenocorticotropic hormone-independent bilateral adrenocortical macronodular hyperplasia: a case report and immunohistochemical studies. , 1994, Endocrine journal.

[4]  T. Saruta,et al.  Adrenocorticotropic hormone-independent bilateral adrenocortical macronodular hyperplasia as a distinct subtype of Cushing's syndrome. Enzyme histochemical and ultrastructural study of four cases with a review of the literature. , 1991, American journal of clinical pathology.

[5]  S. Makino,et al.  Cushing's syndrome due to huge nodular adrenocortical hyperplasia with fluctuation of urinary 17-OHCS excretion. , 1989, Endocrinologia japonica.

[6]  W. Travis,et al.  Primary Adrenal Causes of Cushing's Syndrome; Diagnosis and Surgical Management , 1989, Annals of surgery.

[7]  D. Page,et al.  Adrenocorticotropin-independent bilateral macronodular adrenal hyperplasia: an unusual cause of Cushing's syndrome. , 1989, The Journal of clinical endocrinology and metabolism.

[8]  M. Sepe,et al.  "GIANT" macronodular adrenal hyperplasia causing Cushing's syndrome: case report and review of the literature on a clinical distinction of adrenocortical nodular pathology associated with hypercortisolism. , 1989, Endocrinologia japonica.

[9]  M. Westphal,et al.  Cushing's syndrome due to bilateral adrenal macronodular hyperplasia with undetectable ACTH: cell culture of adenoma cells on extracellular matrix. , 1988, Hormone research.

[10]  K. Hashimoto,et al.  Cortisol responsiveness to insulin-induced hypoglycemia in Cushing's syndrome with huge nodular adrenocortical hyperplasia. , 1986, Endocrinologia japonica.

[11]  D. Aron,et al.  Pituitary ACTH dependency of nodular adrenal hyperplasia in Cushing's syndrome. Report of two cases and review of the literature. , 1981, The American journal of medicine.

[12]  H. Hidai,et al.  Cushing's syndrome due to huge adrenocortical multinodular hyperplasia. , 1975, Endocrinologia japonica.