W. D. Drucker, M.D.; N. P. Christy, M.D.
Drucker WD, Christy NP. Evidence of Persistent Abnormal Pituitary-adrenal Relationship in Patients Subtotally Adrenalectomized for Cushing's Syndrome.. Ann Intern Med. 1963;58:721-722. doi: 10.7326/0003-4819-58-4-721_3
Download citation file:
Published: Ann Intern Med. 1963;58(4):721-722.
This content is PDF only. Please click on the PDF icon to access.
Patients J. J. and D.W., bilaterally subtotally adrenalectomized for Cushing's disease (bilateral adrenal hyperplasia) 7 and 6 years before study, lacked pituitary tumors and were not hyperadrenal as shown by: clinical remission, normal excretion of urinary 17-ketogenic steroids (19 and 12 mg/day) and 17-ketosteroids (13 and 8 mg/day), normal secretory rate of cortisol (20 and 19 mg/day, isotope dilution method), and normal resting levels of plasma cortisol (13 and 11 μg/100 ml). Evidence of abnormal adenohypophysial regulation of adrenal cortical secretion included: total absence of circadian variation in levels of plasma cortisol; failure to respond by increased steroidogenesis
Learn more about subscription options.
Register Now for a free account.
Adrenal Disorders, Endocrine and Metabolism.
Results provided by:
Copyright © 2017 American College of Physicians. All Rights Reserved.
Print ISSN: 0003-4819 | Online ISSN: 1539-3704
Conditions of Use
This PDF is available to Subscribers Only