INTRODUCTIONWe present a rare variety of adrenocorticotrophic hormone (ACTH)-independent Cushing's syndrome known as primary pigmented nodular adrenocortical disease (PPNAD).

CLINICAL PICTUREThe patient initially underwent unilateral adrenalectomy for what was thought to be a left adrenal adenoma.

OUTCOMEPartial resolution of symptoms and demonstrable persistent hypercortisolism after surgery prompted further evaluation with findings leading to the diagnosis of Carney complex. A review of the adrenal histology was consistent with PPNAD.

CONCLUSIONThis entity of PPNAD, which has rarely been reported in Asians, forms part of the Carney complex. The diagnosis may not be simple and straightforward, as illustrated in this patient.

Adrenal Glands ; diagnostic imaging ; Adrenalectomy ; Adrenocortical Hyperfunction ; physiopathology ; Adrenocorticotropic Hormone ; metabolism ; Adult ; Bone Density ; Cushing Syndrome ; diagnosis ; metabolism ; physiopathology ; Female ; Humans ; Tomography, X-Ray Computed