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- W2408954455 abstract "Introduction: We present a rare variety of adrenocorticotrophic hormone (ACTH)-independent Cushing’s syndrome known as primary pigmented nodular adrenocortical disease (PPNAD). Clinical Picture: The patient initially underwent unilateral adrenalectomy for what was thought to be a left adrenal adenoma. Outcome: Partial 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. Conclusion: This 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." @default.
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- W2408954455 date "2006-12-15" @default.
- W2408954455 modified "2023-10-03" @default.
- W2408954455 title "Unravelling the Mystery in a Case of Persistent ACTH-independent Cushing’s Syndrome" @default.
- W2408954455 doi "https://doi.org/10.47102/annals-acadmedsg.v35n12p892" @default.
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