CUSHING'S SYNDROME INTERPRETED AS HYPERADRENOCORTICISM LEADING TO HYPERGLUCONEOGENESIS: RESULTS OF TREATMENT WITH TESTOSTERONE PROPIONATE1
- 1 May 1941
- journal article
- research article
- Published by The Endocrine Society in Journal of Clinical Endocrinology & Metabolism
- Vol. 1 (5), 375-384
- https://doi.org/10.1210/jcem-1-5-375
Abstract
Testosterone propionate therapy in 3 cases of Cushing''s syndrome, without adrenal cancer, resulted in prompt retention of N (about 20 g. in 5 days), prompt retention of P, the ratio of retained N to retained P being approx. their ratio in protein, a gradually decreasing urinary Ca excretion, with a gradually increasing Ca balance, a delayed rise in serum phosphatase level. Associated with the marked N retention were the following clinical changes: increase in strength and wt., decrease in redness of the skin and loss of easy bruisability. Estradiol benzoate did not beneficially alter the N, P or Ca balances, nor in conjunction with testosterone did it alter the beneficial effect of that agent alone. Progesterone had a slightly beneficial effect but it was much inferior to testosterone.This publication has 1 reference indexed in Scilit: