Boy with central precocious puberty probably due to a peripheral cause

BMJ Case Rep. 2016 Jun 2:2016:bcr2016214554. doi: 10.1136/bcr-2016-214554.

Abstract

A 6½ years Indian boy was brought by his parents, who were anxious about the excessive increase in the size of the boy's phallus, from the age of 2 years. On physical examination, the child had a penis length greater than the 97th centile for age, a sexual maturity rating of gonads at stage 2 and pubic hair at stage 3, with height in the high normal range (90-97th centile). The bone age was 12 years. Laboratory evaluation showed pubertal levels of testosterone and pubertal gonadotropin response to stimulation, confirming central precocious puberty (CPP). Incidentally, the hormonal profile also suggested congenital adrenal hyperplasia (CAH). This case report depicts a case of CPP probably caused by CAH in boys, which is rare.

Publication types

  • Case Reports

MeSH terms

  • Adrenal Hyperplasia, Congenital / complications*
  • Adrenal Hyperplasia, Congenital / diagnostic imaging
  • Adrenal Hyperplasia, Congenital / drug therapy
  • Child
  • Gonadotropin-Releasing Hormone / metabolism
  • Humans
  • Hydrocortisone / therapeutic use
  • Luteinizing Hormone / therapeutic use
  • Male
  • Puberty, Precocious / diagnostic imaging
  • Puberty, Precocious / etiology*
  • Testosterone / blood
  • Ultrasonography

Substances

  • Gonadotropin-Releasing Hormone
  • Testosterone
  • Luteinizing Hormone
  • Hydrocortisone