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Corticotroph Adenomas

Cushing’s Disease and Nelson’s Syndrome

  • Chapter
Diagnosis and Management of Pituitary Tumors

Abstract

In 1932, Harvey Cushing published a report of 12 cases in which he described the metabolic derangements associated with pituitary basophilic adenomas, characterizing the syndrome that was later to bear his name (1). The term Cushing’s syndrome refers to the clinical manifestations of glucocorticoid excess regardless of specific etiology, whereas Cushing’s disease refers to those cases of Cushing’s syndrome secondary to pituitary adrenocorticotropic hormone (ACTH) hypersecretion. In the adult population, Cushing’s disease accounts for approx 70% of patients with endogenous Cushing’s syndrome, whereas the remaining 30% are attributable to the ectopic ACTH syndrome and primary adrenal tumors (2).

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Lo, J.C., Tyrrell, J.B., Wilson, C.B. (2001). Corticotroph Adenomas. In: Thapar, K., Kovacs, K., Scheithauer, B.W., Lloyd, R.V. (eds) Diagnosis and Management of Pituitary Tumors. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-217-3_18

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