Cushing's syndrome due to primary multinodular corticotrope hyperplasia.

Abstract

In this report, a case of Cushing's syndrome due to primary multinodular corticotrope hyperplasia is described. The patient had typical features of Cushing's syndrome and dynamic pituitary-adrenal testing, which suggested an ectopic adrenocorticotropic hormone (ACTH) syndrome. Results of petrosal sinus catheterization indicated that the pituitary gland was the source of excess ACTH. Total hypophysectomy resulted in complete remission of Cushing's syndrome. Light microscopic and immunohistochemical studies revealed multinodular corticotrope hyperplasia. Plasma corticotropin releasing hormone (CRH) was undetectable, and computed tomography of the chest and abdomen disclosed no neoplastic source of CRH. We speculate that either an abnormality in hypothalamic CRH secretion or corticotrope hypersensitivity to CRH might have been responsible for Cushing's syndrome in this patient.

• Authors: W F Young Jr, B W Scheithauer, H Gharib, E R Laws Jr, P C Carpenter
• Journal: Mayo Clinic proceedings (Mayo Clin Proc) Vol. 63 Issue 3 Pg. 256-62 (Mar 1988) ISSN: 0025-6196 [Print] England
• PMID: 2830441 (Publication Type: Case Reports, Journal Article, Review)

Chemical References

• Adrenocorticotropic Hormone

Topics

• Adrenocorticotropic Hormone (blood)
• Cushing Syndrome (blood, etiology)
• Female
• Humans
• Hyperplasia
• Middle Aged
• Pituitary Gland (pathology)