Combined treatment with bicalutamide and anastrozole in a young boy with peripheral precocious puberty due to McCune-Albright Syndrome

Endocrine Journal

Francesca Verna¹  Patrizia Matarazzo¹  Roberto Lala¹  Daniele Tessaris¹  Alessandro Mussa¹  Gerdi Tuli¹  Ludovica Fiore¹ 

[1] Department of Pediatric Endocrinology and Diabetology, University of Torino, Regina Margherita Children’s Hospital, Italy

关键词: Bicalutamide;    Anastrozole;    Peripheral precocious puberty;    McCune-Albright;    GSα protein;   

DOI  :  10.1507/endocrj.EJ11-0214

学科分类：内分泌与代谢学

来源: Japan Endocrine Society

【 摘 要 】

References(30)McCune-Albright Syndrome (MAS) is a congenital endocrine disorder due to mosaic tissutal hyper-function.We describe a boy with a molecularly confirmed MAS, clinically evident with congenital café-au-lait spots, bone fibrous dysplasia, hyperthyroidism, and renal phosphate wasting syndrome.At 4.6 years of age he disclosed a rapid progression of peripheral puberty, so we decided to treat him with bicalutamide 25 mg/day and anastrozole 1 mg/day.Combined third generation aromatase inhibitors - competitive androgen receptor blockers were employed in familial male precocious puberty (FMPP).Combined treatment was performed for 49 months from the age of 4.6 to 6.7 years.The patient underwent clinical, laboratory, and instrumental evaluation twice a year from the first admission to the current age.This treatment caused a rapid normalization of growth velocity, subsequent reduction of penile androgenization, and stabilization of testicular volume.The therapy was well tolerated for all its duration and neither side effects, nor secondary hypothalamic activation were noted.This report provides further evidence of effectiveness and safety of combined third generation aromatase inhibitors - competitive androgen receptor blockers in male precocious peripheral puberty, firstly employed in male MAS, and contributes to expand the spectrum of disorders in which their employment may reveal promising.

【 授权许可】

Unknown