Treatment of Familial Male Precocious Puberty with Spironolactone and Testolactone
- 23 February 1989
- journal article
- research article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 320 (8), 496-502
- https://doi.org/10.1056/nejm198902233200805
Abstract
Because the pubertal growth spurt in boys appears to be mediated by both androgens and estrogens, we hypothesized that blockade of both androgen action and estrogen synthesis would normalize the growth of boys with familial male precocious puberty. To test this hypothesis, we studied nine boys (age range, 3.3 to 7.7 years) during treatment with an antiandrogen (spironolactone) or an inhibitor of androgen-to-estrogen conversion (testolactone), followed by treatment with both agents. After six months of observation without treatment, the first four boys received spironolactone for six months, followed by spironolactone and testolactone. The next five boys received testolactone for six months, followed by spironolactone and testolactone.This publication has 30 references indexed in Scilit:
- Gonadotropin-Independent Precocious Puberty (“Testotoxicosis”): Influence of Maturational Status on Response to KetoconazoleJournal of Clinical Endocrinology & Metabolism, 1987
- Familial male precocious puberty in 3 generationsActa Endocrinologica, 1986
- Ketoconazole in the Management of Precocious Puberty Not Responsive to LHRH-Analogue TherapyNew England Journal of Medicine, 1985
- Puberty without GonadotropinsNew England Journal of Medicine, 1985
- Male-Limited Familial Precocious Puberty in Three GenerationsNew England Journal of Medicine, 1984
- Long-Term Treatment of Central Precocious Puberty with a Long-Acting Analogue of Luteinizing Hormone-Releasing HormoneNew England Journal of Medicine, 1983
- Gonadotropin-Independent Familial Sexual Precocity with Premature Leydig and Germinal Cell Maturation (Familial Testotoxicosis): Effects of a Potent Luteinizing Hormone-Releasing Factor Agonist and Medroxyprogesterone Acetate Therapy in Four Cases*Journal of Clinical Endocrinology & Metabolism, 1983
- Short-Term Treatment of Idiopathic Precocious Puberty with a Long-Acting Analogue of Luteinizing Hormone-Releasing HormoneNew England Journal of Medicine, 1981
- Testicular Leydig Cell Hyperplasia as a Cause of Familial Sexual Precocity*Journal of Clinical Endocrinology & Metabolism, 1981
- Familial Male Sexual Precocity: Report of the Eleventh Kindred Found, with Observations on Blood Group Linkage and Urinary C19-Steroid ExcretionJournal of Clinical Endocrinology & Metabolism, 1962