Author:
Tamm J.,Voigt K. D.,Kracht J.
Abstract
ABSTRACT
A case report is given of a patient with Cushing's syndrome due to bilateral adrenocortical hyperplasia. The 17-OHCS in plasma showed only a low or none response to corticotrophin (ACTH), administered intravenously. The elevated excretion of 17-OHCS in urine exhibited a further increase following the first ACTH administration, but were not depressed significantly after 120 mg triamcinolone within four days. No reaction of urinary 17-OHCS was seen following a second ACTH-infusion. A plausible explanation for these phenomena can not be given.
After bilateral adrenalectomy measurable amounts of 17-OHCS were excreted in urine, probably reflecting the steroid secretion of aberrant adrenal cortical tissue. Plasma clearance of exogenous cortisol was some-what delayed without disturbed formation of conjugated steroids.
Postoperative well-being of the patient was achieved only by treatment with the 21-deoxysteroid oxylone or with triamcinolone combined with deoxycorticosterone acetate.
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
6 articles.
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