ECTOPIC ACTH SYNDROME AND CRH-MEDIATED CUSHINGS-SYNDROME

Authors
Citation
M. Becker et Dc. Aron, ECTOPIC ACTH SYNDROME AND CRH-MEDIATED CUSHINGS-SYNDROME, Endocrinology and metabolism clinics of North America, 23(3), 1994, pp. 585-606
Citations number
179
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
08898529
Volume
23
Issue
3
Year of publication
1994
Pages
585 - 606
Database
ISI
SICI code
0889-8529(1994)23:3<585:EASACC>2.0.ZU;2-D
Abstract
The ectopic ACTH syndrome accounts for a substantial number of patient s with naturally occurring Cushing's syndrome. Patients with either ec topic ACTH syndrome or the rare CRH-mediated Cushing's syndrome may be indistinguishable from patients with pituitary ACTH Cushing's syndrom e, based on clinical grounds or simple biochemical and radiologic test ing. Because their therapies differ, accurate diagnosis is essential. While clinical researchers continue to develop more effective diagnost ic techniques and therapies, further advances in the molecular and cel l biology of ACTH and CRH-producing tumors will undoubtedly shed light on the pathogenesis of this perplexing, fascinating, and controversia l entity.